Join a respected agricultural manufacturing business as a Product Quality Control Technician in Banbury. This part-time role offers hands-on experience in quality assurance, laboratory testing, and production support within the animal feed industry. Product Quality Control TechnicianBanbury, Oxfordshire Part time, 25 hours per week, Monday - Friday with flexible scheduling Permanent position Competitive hourly rate Please note: Applicants must be authorised to work in the UK Our client is a well-established supplier of high-quality animal feed ingredients, serving the broiler, layer and pig feed markets across the UK. With more than 60 years of industry expertise, the company has built a strong reputation for delivering reliable products, excellent customer service, and innovative solutions within feed manufacturing and grain trading. The Role They are looking for a Product Quality Control Technician to join the team at the Banbury manufacturing site. This varied role plays an important part in ensuring the quality, integrity and traceability of feed products and raw materials. Key Responsibilities: Conduct quality control tests on incoming raw materials and finished products, including oils, protein and moisture testing Ensure compliance with FEMAS quality accreditation standards and internal company procedures Maintain and organise the laboratory environment, ensuring it remains clean, safe and efficient Collect and prepare samples for external laboratory analysis and liaise with laboratories and colleagues to support quality processes Inspect the condition of stored products and raw materials to maintain product integrity Manage and maintain the engineering stock database, ensuring spare parts and materials remain at agreed stock levels Provide administrative support, including ordering spare parts and maintaining records Oversee the rotation of finished products in storage to maintain quality standards Provide operational cover for the weighbridge when required Support quality audits conducted by customers and accreditation bodies Carry out additional duties as required to support production and quality teams The Ideal Candidate The ideal candidate will be organised, detail-oriented and capable of working both independently and collaboratively within a production environment. About you: Good general education with strong written and spoken English Competent in mathematics and scientific principles Comfortable using Microsoft Excel, Word and general computer systems Ideally educated to A Level standard or equivalent Previous experience in quality control, laboratory work or manufacturing is beneficial but not essential Strong attention to detail and accuracy Excellent organisational skills and tidy working practices Ability to work both independently and as part of a team Flexible attitude and willingness to support colleagues across departments Knowledge of the agricultural or feed manufacturing industry would be advantageous Benefits: Competitive hourly wage Permanent part-time position (25 hours per week) with flexible working schedule Supportive and friendly workplace culture Full training provided Opportunities to develop skills in quality assurance, laboratory testing and feed production processes How to apply for the role: If you have the skills and experience required for this position, click "apply" today and check your inbox for an email providing more information on how to complete your application and provide any other supporting documents. You must be authorised to work in the UK. No agencies, please. Other suitable skills and experience include Quality Control Assistant, Laboratory Technician, QA Technician, Quality Assurance Assistant, Production Operative, Food Safety Technician, Manufacturing Assistant, QC Operative, Process Technician, Materials Testing Technician.
Mar 16, 2026
Full time
Join a respected agricultural manufacturing business as a Product Quality Control Technician in Banbury. This part-time role offers hands-on experience in quality assurance, laboratory testing, and production support within the animal feed industry. Product Quality Control TechnicianBanbury, Oxfordshire Part time, 25 hours per week, Monday - Friday with flexible scheduling Permanent position Competitive hourly rate Please note: Applicants must be authorised to work in the UK Our client is a well-established supplier of high-quality animal feed ingredients, serving the broiler, layer and pig feed markets across the UK. With more than 60 years of industry expertise, the company has built a strong reputation for delivering reliable products, excellent customer service, and innovative solutions within feed manufacturing and grain trading. The Role They are looking for a Product Quality Control Technician to join the team at the Banbury manufacturing site. This varied role plays an important part in ensuring the quality, integrity and traceability of feed products and raw materials. Key Responsibilities: Conduct quality control tests on incoming raw materials and finished products, including oils, protein and moisture testing Ensure compliance with FEMAS quality accreditation standards and internal company procedures Maintain and organise the laboratory environment, ensuring it remains clean, safe and efficient Collect and prepare samples for external laboratory analysis and liaise with laboratories and colleagues to support quality processes Inspect the condition of stored products and raw materials to maintain product integrity Manage and maintain the engineering stock database, ensuring spare parts and materials remain at agreed stock levels Provide administrative support, including ordering spare parts and maintaining records Oversee the rotation of finished products in storage to maintain quality standards Provide operational cover for the weighbridge when required Support quality audits conducted by customers and accreditation bodies Carry out additional duties as required to support production and quality teams The Ideal Candidate The ideal candidate will be organised, detail-oriented and capable of working both independently and collaboratively within a production environment. About you: Good general education with strong written and spoken English Competent in mathematics and scientific principles Comfortable using Microsoft Excel, Word and general computer systems Ideally educated to A Level standard or equivalent Previous experience in quality control, laboratory work or manufacturing is beneficial but not essential Strong attention to detail and accuracy Excellent organisational skills and tidy working practices Ability to work both independently and as part of a team Flexible attitude and willingness to support colleagues across departments Knowledge of the agricultural or feed manufacturing industry would be advantageous Benefits: Competitive hourly wage Permanent part-time position (25 hours per week) with flexible working schedule Supportive and friendly workplace culture Full training provided Opportunities to develop skills in quality assurance, laboratory testing and feed production processes How to apply for the role: If you have the skills and experience required for this position, click "apply" today and check your inbox for an email providing more information on how to complete your application and provide any other supporting documents. You must be authorised to work in the UK. No agencies, please. Other suitable skills and experience include Quality Control Assistant, Laboratory Technician, QA Technician, Quality Assurance Assistant, Production Operative, Food Safety Technician, Manufacturing Assistant, QC Operative, Process Technician, Materials Testing Technician.
Quality Assurance (QA) Manager Medical Device manufacturer. Based Northern UK - M62 / M1 circa Manchester, Leeds, Sheffield, Doncaster Base salary £60-70k (Negotiable) with Bonus and Package. Role Overview Our client is a global medical device manufacturer seeking an experienced and hands-on Quality Assurance Manager to lead their Quality function in a regulated manufacturing environment. This role is ideal for a Quality professional from the medical device, pharmaceutical, or chemical manufacturing sectors who can operate strategically and practically - including close collaboration with laboratory teams to support QA testing and compliance. The QA Manager will ensure regulatory compliance, maintain a robust Quality Management System (QMS), and drive a culture of quality, safety, and continuous improvement across the business. Office access required 2-3 days a week. Key Responsibilities Quality Management & Compliance Lead, maintain, and continuously improve the QMS in line with: ISO 9001 ISO 14001 GMP standards (applicable to the sector) UK MDR (for medical device components, if applicable) Ensure audit readiness at all times and maintain accurate quality records. Manage document control, change control, and staff training compliance systems. Lead Management Review and report on key quality metrics and KPIs. One direct head reports into the QA Manager. Laboratory & Product Quality Oversight Work closely with laboratory teams to oversee QA testing processes. Ensure handling, testing, and documentation of products meet regulatory and safety standards. Integrate quality systems within lab operations to maintain data integrity, traceability, and compliance. Support method validation, stability studies, and product testing as required. GMP & Audit Leadership Lead internal and supplier audits, ensuring effective follow-up and closure of CAPAs. Prepare for and support external audits from certification bodies, MHRA, or other regulatory authorities. Implement and oversee GMP standards across production and laboratory operations. HACCP & Environmental Compliance Maintain and develop HACCP systems where relevant. Ensure environmental compliance aligned with ISO 14001 standards. Monitor and drive improvements in environmental, safety, and quality performance. Key Requirements Proven experience as a Quality Manager in medical device, pharmaceutical, or chemical manufacturing. Strong understanding of laboratory QA testing and ability to integrate with lab teams. Practical experience with: ISO 9001 ISO 14001 HACCP GMP standards Experience leading and managing internal and external audits. Strong knowledge of risk management, CAPA processes, and regulatory compliance. Excellent organisational, leadership, and communication skills. Personal Attributes Detail-oriented, proactive, and solutions-focused. Comfortable working strategically and hands-on. Confident engaging with auditors, regulators, and cross-functional teams. Committed to fostering a culture of compliance, accountability, and continuous improvement. Why Join? Leadership role with visible impact on quality, compliance, and operational excellence. Opportunity to work across multiple regulated sectors - medical device, pharmaceutical, and chemical manufacturing. Collaborative culture with close integration between lab, production, and operations. Competitive salary and benefits package.
Mar 16, 2026
Full time
Quality Assurance (QA) Manager Medical Device manufacturer. Based Northern UK - M62 / M1 circa Manchester, Leeds, Sheffield, Doncaster Base salary £60-70k (Negotiable) with Bonus and Package. Role Overview Our client is a global medical device manufacturer seeking an experienced and hands-on Quality Assurance Manager to lead their Quality function in a regulated manufacturing environment. This role is ideal for a Quality professional from the medical device, pharmaceutical, or chemical manufacturing sectors who can operate strategically and practically - including close collaboration with laboratory teams to support QA testing and compliance. The QA Manager will ensure regulatory compliance, maintain a robust Quality Management System (QMS), and drive a culture of quality, safety, and continuous improvement across the business. Office access required 2-3 days a week. Key Responsibilities Quality Management & Compliance Lead, maintain, and continuously improve the QMS in line with: ISO 9001 ISO 14001 GMP standards (applicable to the sector) UK MDR (for medical device components, if applicable) Ensure audit readiness at all times and maintain accurate quality records. Manage document control, change control, and staff training compliance systems. Lead Management Review and report on key quality metrics and KPIs. One direct head reports into the QA Manager. Laboratory & Product Quality Oversight Work closely with laboratory teams to oversee QA testing processes. Ensure handling, testing, and documentation of products meet regulatory and safety standards. Integrate quality systems within lab operations to maintain data integrity, traceability, and compliance. Support method validation, stability studies, and product testing as required. GMP & Audit Leadership Lead internal and supplier audits, ensuring effective follow-up and closure of CAPAs. Prepare for and support external audits from certification bodies, MHRA, or other regulatory authorities. Implement and oversee GMP standards across production and laboratory operations. HACCP & Environmental Compliance Maintain and develop HACCP systems where relevant. Ensure environmental compliance aligned with ISO 14001 standards. Monitor and drive improvements in environmental, safety, and quality performance. Key Requirements Proven experience as a Quality Manager in medical device, pharmaceutical, or chemical manufacturing. Strong understanding of laboratory QA testing and ability to integrate with lab teams. Practical experience with: ISO 9001 ISO 14001 HACCP GMP standards Experience leading and managing internal and external audits. Strong knowledge of risk management, CAPA processes, and regulatory compliance. Excellent organisational, leadership, and communication skills. Personal Attributes Detail-oriented, proactive, and solutions-focused. Comfortable working strategically and hands-on. Confident engaging with auditors, regulators, and cross-functional teams. Committed to fostering a culture of compliance, accountability, and continuous improvement. Why Join? Leadership role with visible impact on quality, compliance, and operational excellence. Opportunity to work across multiple regulated sectors - medical device, pharmaceutical, and chemical manufacturing. Collaborative culture with close integration between lab, production, and operations. Competitive salary and benefits package.
Quality Assurance (QA) Manager Medical Device manufacturer. Based Northern UK - M62 / M1 circa Manchester, Leeds, Sheffield, Doncaster Base salary £60-70k (Negotiable) with Bonus and Package. Role Overview Our client is a global medical device manufacturer seeking an experienced and hands-on Quality Assurance Manager to lead their Quality function in a regulated manufacturing environment. This role is ideal for a Quality professional from the medical device, pharmaceutical, or chemical manufacturing sectors who can operate strategically and practically - including close collaboration with laboratory teams to support QA testing and compliance. The QA Manager will ensure regulatory compliance, maintain a robust Quality Management System (QMS), and drive a culture of quality, safety, and continuous improvement across the business. Office access required 2-3 days a week. Key Responsibilities Quality Management & Compliance Lead, maintain, and continuously improve the QMS in line with: ISO 9001 ISO 14001 GMP standards (applicable to the sector) UK MDR (for medical device components, if applicable) Ensure audit readiness at all times and maintain accurate quality records. Manage document control, change control, and staff training compliance systems. Lead Management Review and report on key quality metrics and KPIs. One direct head reports into the QA Manager. Laboratory & Product Quality Oversight Work closely with laboratory teams to oversee QA testing processes. Ensure handling, testing, and documentation of products meet regulatory and safety standards. Integrate quality systems within lab operations to maintain data integrity, traceability, and compliance. Support method validation, stability studies, and product testing as required. GMP & Audit Leadership Lead internal and supplier audits, ensuring effective follow-up and closure of CAPAs. Prepare for and support external audits from certification bodies, MHRA, or other regulatory authorities. Implement and oversee GMP standards across production and laboratory operations. HACCP & Environmental Compliance Maintain and develop HACCP systems where relevant. Ensure environmental compliance aligned with ISO 14001 standards. Monitor and drive improvements in environmental, safety, and quality performance. Key Requirements Proven experience as a Quality Manager in medical device, pharmaceutical, or chemical manufacturing. Strong understanding of laboratory QA testing and ability to integrate with lab teams. Practical experience with: ISO 9001 ISO 14001 HACCP GMP standards Experience leading and managing internal and external audits. Strong knowledge of risk management, CAPA processes, and regulatory compliance. Excellent organisational, leadership, and communication skills. Personal Attributes Detail-oriented, proactive, and solutions-focused. Comfortable working strategically and hands-on. Confident engaging with auditors, regulators, and cross-functional teams. Committed to fostering a culture of compliance, accountability, and continuous improvement. Why Join? Leadership role with visible impact on quality, compliance, and operational excellence. Opportunity to work across multiple regulated sectors - medical device, pharmaceutical, and chemical manufacturing. Collaborative culture with close integration between lab, production, and operations. Competitive salary and benefits package.
Mar 16, 2026
Full time
Quality Assurance (QA) Manager Medical Device manufacturer. Based Northern UK - M62 / M1 circa Manchester, Leeds, Sheffield, Doncaster Base salary £60-70k (Negotiable) with Bonus and Package. Role Overview Our client is a global medical device manufacturer seeking an experienced and hands-on Quality Assurance Manager to lead their Quality function in a regulated manufacturing environment. This role is ideal for a Quality professional from the medical device, pharmaceutical, or chemical manufacturing sectors who can operate strategically and practically - including close collaboration with laboratory teams to support QA testing and compliance. The QA Manager will ensure regulatory compliance, maintain a robust Quality Management System (QMS), and drive a culture of quality, safety, and continuous improvement across the business. Office access required 2-3 days a week. Key Responsibilities Quality Management & Compliance Lead, maintain, and continuously improve the QMS in line with: ISO 9001 ISO 14001 GMP standards (applicable to the sector) UK MDR (for medical device components, if applicable) Ensure audit readiness at all times and maintain accurate quality records. Manage document control, change control, and staff training compliance systems. Lead Management Review and report on key quality metrics and KPIs. One direct head reports into the QA Manager. Laboratory & Product Quality Oversight Work closely with laboratory teams to oversee QA testing processes. Ensure handling, testing, and documentation of products meet regulatory and safety standards. Integrate quality systems within lab operations to maintain data integrity, traceability, and compliance. Support method validation, stability studies, and product testing as required. GMP & Audit Leadership Lead internal and supplier audits, ensuring effective follow-up and closure of CAPAs. Prepare for and support external audits from certification bodies, MHRA, or other regulatory authorities. Implement and oversee GMP standards across production and laboratory operations. HACCP & Environmental Compliance Maintain and develop HACCP systems where relevant. Ensure environmental compliance aligned with ISO 14001 standards. Monitor and drive improvements in environmental, safety, and quality performance. Key Requirements Proven experience as a Quality Manager in medical device, pharmaceutical, or chemical manufacturing. Strong understanding of laboratory QA testing and ability to integrate with lab teams. Practical experience with: ISO 9001 ISO 14001 HACCP GMP standards Experience leading and managing internal and external audits. Strong knowledge of risk management, CAPA processes, and regulatory compliance. Excellent organisational, leadership, and communication skills. Personal Attributes Detail-oriented, proactive, and solutions-focused. Comfortable working strategically and hands-on. Confident engaging with auditors, regulators, and cross-functional teams. Committed to fostering a culture of compliance, accountability, and continuous improvement. Why Join? Leadership role with visible impact on quality, compliance, and operational excellence. Opportunity to work across multiple regulated sectors - medical device, pharmaceutical, and chemical manufacturing. Collaborative culture with close integration between lab, production, and operations. Competitive salary and benefits package.
Quality Assurance (QA) Manager Medical Device manufacturer. Based Northern UK - M62 / M1 circa Manchester, Leeds, Sheffield, Doncaster Base salary £60-70k (Negotiable) with Bonus and Package. Role Overview Our client is a global medical device manufacturer seeking an experienced and hands-on Quality Assurance Manager to lead their Quality function in a regulated manufacturing environment. This role is ideal for a Quality professional from the medical device, pharmaceutical, or chemical manufacturing sectors who can operate strategically and practically - including close collaboration with laboratory teams to support QA testing and compliance. The QA Manager will ensure regulatory compliance, maintain a robust Quality Management System (QMS), and drive a culture of quality, safety, and continuous improvement across the business. Office access required 2-3 days a week. Key Responsibilities Quality Management & Compliance Lead, maintain, and continuously improve the QMS in line with: ISO 9001 ISO 14001 GMP standards (applicable to the sector) UK MDR (for medical device components, if applicable) Ensure audit readiness at all times and maintain accurate quality records. Manage document control, change control, and staff training compliance systems. Lead Management Review and report on key quality metrics and KPIs. One direct head reports into the QA Manager. Laboratory & Product Quality Oversight Work closely with laboratory teams to oversee QA testing processes. Ensure handling, testing, and documentation of products meet regulatory and safety standards. Integrate quality systems within lab operations to maintain data integrity, traceability, and compliance. Support method validation, stability studies, and product testing as required. GMP & Audit Leadership Lead internal and supplier audits, ensuring effective follow-up and closure of CAPAs. Prepare for and support external audits from certification bodies, MHRA, or other regulatory authorities. Implement and oversee GMP standards across production and laboratory operations. HACCP & Environmental Compliance Maintain and develop HACCP systems where relevant. Ensure environmental compliance aligned with ISO 14001 standards. Monitor and drive improvements in environmental, safety, and quality performance. Key Requirements Proven experience as a Quality Manager in medical device, pharmaceutical, or chemical manufacturing. Strong understanding of laboratory QA testing and ability to integrate with lab teams. Practical experience with: ISO 9001 ISO 14001 HACCP GMP standards Experience leading and managing internal and external audits. Strong knowledge of risk management, CAPA processes, and regulatory compliance. Excellent organisational, leadership, and communication skills. Personal Attributes Detail-oriented, proactive, and solutions-focused. Comfortable working strategically and hands-on. Confident engaging with auditors, regulators, and cross-functional teams. Committed to fostering a culture of compliance, accountability, and continuous improvement. Why Join? Leadership role with visible impact on quality, compliance, and operational excellence. Opportunity to work across multiple regulated sectors - medical device, pharmaceutical, and chemical manufacturing. Collaborative culture with close integration between lab, production, and operations. Competitive salary and benefits package.
Mar 16, 2026
Full time
Quality Assurance (QA) Manager Medical Device manufacturer. Based Northern UK - M62 / M1 circa Manchester, Leeds, Sheffield, Doncaster Base salary £60-70k (Negotiable) with Bonus and Package. Role Overview Our client is a global medical device manufacturer seeking an experienced and hands-on Quality Assurance Manager to lead their Quality function in a regulated manufacturing environment. This role is ideal for a Quality professional from the medical device, pharmaceutical, or chemical manufacturing sectors who can operate strategically and practically - including close collaboration with laboratory teams to support QA testing and compliance. The QA Manager will ensure regulatory compliance, maintain a robust Quality Management System (QMS), and drive a culture of quality, safety, and continuous improvement across the business. Office access required 2-3 days a week. Key Responsibilities Quality Management & Compliance Lead, maintain, and continuously improve the QMS in line with: ISO 9001 ISO 14001 GMP standards (applicable to the sector) UK MDR (for medical device components, if applicable) Ensure audit readiness at all times and maintain accurate quality records. Manage document control, change control, and staff training compliance systems. Lead Management Review and report on key quality metrics and KPIs. One direct head reports into the QA Manager. Laboratory & Product Quality Oversight Work closely with laboratory teams to oversee QA testing processes. Ensure handling, testing, and documentation of products meet regulatory and safety standards. Integrate quality systems within lab operations to maintain data integrity, traceability, and compliance. Support method validation, stability studies, and product testing as required. GMP & Audit Leadership Lead internal and supplier audits, ensuring effective follow-up and closure of CAPAs. Prepare for and support external audits from certification bodies, MHRA, or other regulatory authorities. Implement and oversee GMP standards across production and laboratory operations. HACCP & Environmental Compliance Maintain and develop HACCP systems where relevant. Ensure environmental compliance aligned with ISO 14001 standards. Monitor and drive improvements in environmental, safety, and quality performance. Key Requirements Proven experience as a Quality Manager in medical device, pharmaceutical, or chemical manufacturing. Strong understanding of laboratory QA testing and ability to integrate with lab teams. Practical experience with: ISO 9001 ISO 14001 HACCP GMP standards Experience leading and managing internal and external audits. Strong knowledge of risk management, CAPA processes, and regulatory compliance. Excellent organisational, leadership, and communication skills. Personal Attributes Detail-oriented, proactive, and solutions-focused. Comfortable working strategically and hands-on. Confident engaging with auditors, regulators, and cross-functional teams. Committed to fostering a culture of compliance, accountability, and continuous improvement. Why Join? Leadership role with visible impact on quality, compliance, and operational excellence. Opportunity to work across multiple regulated sectors - medical device, pharmaceutical, and chemical manufacturing. Collaborative culture with close integration between lab, production, and operations. Competitive salary and benefits package.
Electrical Inspector Location: Waterbeach, Cambridgeshire Salary: £30,000 - £35,000 per annum Hours: Monday-Thursday: 8:00am - 4:30pm, Friday: 8:00am - 1:00pm (On-site role) About the Business Our client is a specialist aerospace manufacturing organisation designing, producing, and supporting advanced aircraft systems for major global airframers. Operating in a highly regulated environment, they pride ourselves on quality, safety, and continuous improvement across everything they do. The Role We are seeking an experienced Electrical Inspector for our client to support the smooth operation of the Quality function. This role plays a key part in ensuring compliance with aerospace standards, minimizing quality costs, and maximizing customer satisfaction through robust inspection, testing, and quality assurance processes. Key Responsibilities Ensure quality activities comply with all health, safety, and environmental policies Contribute to the development and continuous improvement of quality systems and processes Carry out First Article Inspections (FAI) and compile FAI reports Read and interpret complex, multi-level electrical drawings and specifications Perform testing in line with procedures and complete acceptance test reports Conduct electrical testing including continuity, dielectric, insulation, bonding, fault-finding, and functional testing Raise and manage non-conformance reports (NCRs) Liaise with design teams and suppliers to resolve drawing or specification issues Maintain the Quality Management System in line with certifications and regulatory requirements Review quality data to identify process improvement opportunities Ensure ongoing compliance with aerospace regulations and quality standards Support management with the development and maintenance of effective QA systems Willingness to work overtime, including evenings and weekends, when required This role may involve additional duties in line with business needs. Knowledge, Skills & Experience Knowledge: Working knowledge of EASA Part 21 and/or Part 145 Understanding of AS9100 Rev D aerospace quality standards Strong grasp of quality management principles, tools, and techniques Skills & Competencies: Excellent verbal and written communication skills Ability to work independently and as part of a team Strong attention to detail and problem-solving skills Confident engaging with regulatory bodies Proficient in Microsoft Office and general IT systems Experience: Previous experience in a Quality or Electrical Inspection role Working knowledge of Airbus and/or Boeing systems and processes Experience with IFE (In-Flight Entertainment) systems preferred A CQI-approved or other relevant quality qualification is advantageous If you are interested in the role of Electrical Inspector and feel that you have the relevant experience, please contact your Recruitment Partner, Lisa Logan at Unicorn Resourcing on or email If this job isn't exactly right for you but you're looking for something new, please contact us for a confidential career discussion. Unicorn Resourcing Limited is acting as an Employment Agency in regard to this Permanent opportunity.
Mar 16, 2026
Full time
Electrical Inspector Location: Waterbeach, Cambridgeshire Salary: £30,000 - £35,000 per annum Hours: Monday-Thursday: 8:00am - 4:30pm, Friday: 8:00am - 1:00pm (On-site role) About the Business Our client is a specialist aerospace manufacturing organisation designing, producing, and supporting advanced aircraft systems for major global airframers. Operating in a highly regulated environment, they pride ourselves on quality, safety, and continuous improvement across everything they do. The Role We are seeking an experienced Electrical Inspector for our client to support the smooth operation of the Quality function. This role plays a key part in ensuring compliance with aerospace standards, minimizing quality costs, and maximizing customer satisfaction through robust inspection, testing, and quality assurance processes. Key Responsibilities Ensure quality activities comply with all health, safety, and environmental policies Contribute to the development and continuous improvement of quality systems and processes Carry out First Article Inspections (FAI) and compile FAI reports Read and interpret complex, multi-level electrical drawings and specifications Perform testing in line with procedures and complete acceptance test reports Conduct electrical testing including continuity, dielectric, insulation, bonding, fault-finding, and functional testing Raise and manage non-conformance reports (NCRs) Liaise with design teams and suppliers to resolve drawing or specification issues Maintain the Quality Management System in line with certifications and regulatory requirements Review quality data to identify process improvement opportunities Ensure ongoing compliance with aerospace regulations and quality standards Support management with the development and maintenance of effective QA systems Willingness to work overtime, including evenings and weekends, when required This role may involve additional duties in line with business needs. Knowledge, Skills & Experience Knowledge: Working knowledge of EASA Part 21 and/or Part 145 Understanding of AS9100 Rev D aerospace quality standards Strong grasp of quality management principles, tools, and techniques Skills & Competencies: Excellent verbal and written communication skills Ability to work independently and as part of a team Strong attention to detail and problem-solving skills Confident engaging with regulatory bodies Proficient in Microsoft Office and general IT systems Experience: Previous experience in a Quality or Electrical Inspection role Working knowledge of Airbus and/or Boeing systems and processes Experience with IFE (In-Flight Entertainment) systems preferred A CQI-approved or other relevant quality qualification is advantageous If you are interested in the role of Electrical Inspector and feel that you have the relevant experience, please contact your Recruitment Partner, Lisa Logan at Unicorn Resourcing on or email If this job isn't exactly right for you but you're looking for something new, please contact us for a confidential career discussion. Unicorn Resourcing Limited is acting as an Employment Agency in regard to this Permanent opportunity.
About the Role: Grade Level (for internal use): 11 The Team: We are seeking an experienced Research Manager to lead a global team of research analysts responsible for identifying and validating supply chain relationships across the automotive ecosystem. This role will set the research direction, strengthen methodologies, and ensure consistent, high-quality outputs across for the Procurement Intelligence research team. You will join a talented and intellectually curious team of analysts working creatively to build objective insights that automotive procurement and risk stakeholders rely on. S&P Global has recently announced the intent to separate our Mobility Segment into a standalone public company. For more information, visit Responsibilities and Impact: Define and execute the research approach and methodologies used to identify and validate suppliers and supply chain relationships across the automotive ecosystem. Lead and develop a distributed team of research analysts across multiple time zones, setting priorities, managing workloads, and ensuring timely delivery against SLAs and project timelines. Establish research best practices (source triangulation, confidence scoring, documentation standards, audit trails, and escalation paths) to ensure consistency, repeatability, and defensibility of outputs. Guide analysts on data sources and collection strategies, including how to select, evaluate, and triangulate sources to validate supplier relationships and trading activity. Implement quality assurance (QA) and continuous improvement, including regular calibration sessions, spot checks, root cause reviews of defects, and coaching to reduce rework and improve accuracy over time. Collaborate cross functionally with operations, product/development, and commercial teams to align research outputs with platform requirements, client needs, and go to market messaging. Identify new research opportunities that expand coverage and support business growth. Support customer facing engagements as needed, including methodology discussions, research readouts, and responding to client inquiries regarding data provenance and validation logic. What We're Looking For: Basic Required Qualifications: Bachelor's degree in Business, Engineering, Supply Chain Management or a related field. 5+ years of experience in research management, competitive intelligence, supply chain research, or a related role-preferably tied to automotive or global supply chains. Proven experience managing distributed teams (multiple time zones), including performance management, coaching, and operational execution. Demonstrated ability to design research methods and translate ambiguous questions into structured workflows, measurable outputs, and clear analyst instructions. Excellent written and verbal communication skills, including the ability to present research findings and defend methodology to internal and external stakeholders. Additional Preferred Qualifications: Strong understanding of automotive supply chain structures and/or procurement processes (supplier tiers, sourcing, localization, capacity constraints, and operational risk concepts). Domain expertise in Electronics & Semiconductor Systems, Powertrain & Chassis Systems, or Interior & Cabin Systems. Experience partnering with technical teams to operationalise research outputs into scalable datasets. Background in supplier discovery/validation using a mix of primary/secondary research (e.g., interviews, industry publications, trade data, corporate filings, customs/shipping signals). Experience building or managing quality programs (QA frameworks, rubrics, confidence scoring, SOPs, training curricula). Track record of publishing research (reports, briefings, client deliverables) or presenting insights to procurement, supply chain, risk, or executive audiences. Familiarity with global trade and compliance concepts relevant to automotive sourcing (e.g., sanctions/export controls exposure, country of origin considerations, forced labor screening workflows). Master's degree (MBA or related) is a plus. Compensation/Benefits Information: (This section is only applicable to US candidates) S&P Global states that the anticipated base salary range for this position is $91,805 to $181,560. Final base salary for this role will be based on the individual's geographic location, as well as experience level, skill set, training, licenses and certifications. In addition to base compensation, this role is eligible for an annual incentive plan. This role is not eligible for additional compensation such as an annual incentive bonus or sales commission plan. This role is eligible to receive additional S&P Global benefits. For more information on the benefits we provide to our employees, please click Here About S&P Global Mobility At S&P Global Mobility, we provide invaluable insights derived from unmatched automotive data, enabling our customers to anticipate change and make decisions with conviction. Our expertise helps them to optimise their businesses, reach the right consumers, and shape the future of mobility. We open the door to automotive innovation, revealing the buying patterns of today and helping customers plan for the emerging technologies of tomorrow. What's In It For You? Our Mission: Advancing Essential Intelligence. Our People: We're more than 35,000 strong worldwide-so we're able to understand nuances while having a broad perspective. Our team is driven by curiosity and a shared belief that Essential Intelligence can help build a more prosperous future for us all. From finding new ways to measure sustainability to analysing energy transition across the supply chain to building workflow solutions that make it easy to tap into insight and apply it. We are changing the way people see things and empowering them to make an impact on the world we live in. We're committed to a more equitable future and to helping our customers find new, sustainable ways of doing business. Join us and help create the critical insights that truly make a difference. Our Values: Integrity, Discovery, Partnership Benefits: We take care of you, so you can take care of business. We care about our people. That's why we provide everything you- and your career-need to thrive at S&P Global. Our benefits include: Health & Wellness: Health care coverage designed for the mind and body. Flexible Downtime: Generous time off helps keep you energized for your time on. Continuous Learning: Access a wealth of resources to grow your career and learn valuable new skills. Invest in Your Future: Secure your financial future through competitive pay, retirement planning, a continuing education programme with a company matched student loan contribution, and financial wellness programmes. Family Friendly Perks: It's not just about you. S&P Global has perks for your partners and little ones, too, with some best in class benefits for families. Beyond the Basics: From retail discounts to referral incentive awards-small perks can make a big difference. For more information on benefits by country visit: Global Hiring and Opportunity at S&P Global: At S&P Global, we are committed to fostering a connected and engaged workplace where all individuals have access to opportunities based on their skills, experience, and contributions. Our hiring practices emphasise fairness, transparency, and merit, ensuring that we attract and retain top talent. By valuing different perspectives and promoting a culture of respect and collaboration, we drive innovation and power global markets. Recruitment Fraud Alert: If you receive an email from a domain or any other regionally based domains, it is a scam and should be reported to . S&P Global never requires any candidate to pay money for job applications, interviews, offer letters, "pre employment training" or for equipment/delivery of equipment. Stay informed and protect yourself from recruitment fraud by reviewing our guidelines, fraudulent domains, and how to report suspicious activity here. Equal Opportunity Employer S&P Global is an equal opportunity employer and all qualified candidates will receive consideration for employment without regard to race/ethnicity, colour, religion, sex, sexual orientation, gender identity, national origin, age, disability, marital status, military veteran status, unemployment status, or any other status protected by law. Only electronic job submissions will be considered for employment. If you need an accommodation during the application process due to a disability, please send an email to: and your request will be forwarded to the appropriate person. US Candidates Only: The EEO is the Law Poster describes discrimination protections under federal law. Pay Transparency Nondiscrimination Provision - English_formattedESQA508c.pdf RESECH103.2 - Middle Management Tier II (EEO Job Group) Job ID: 326237 Posted On: 2026-03-06 Location: Virtual, United Kingdom
Mar 16, 2026
Full time
About the Role: Grade Level (for internal use): 11 The Team: We are seeking an experienced Research Manager to lead a global team of research analysts responsible for identifying and validating supply chain relationships across the automotive ecosystem. This role will set the research direction, strengthen methodologies, and ensure consistent, high-quality outputs across for the Procurement Intelligence research team. You will join a talented and intellectually curious team of analysts working creatively to build objective insights that automotive procurement and risk stakeholders rely on. S&P Global has recently announced the intent to separate our Mobility Segment into a standalone public company. For more information, visit Responsibilities and Impact: Define and execute the research approach and methodologies used to identify and validate suppliers and supply chain relationships across the automotive ecosystem. Lead and develop a distributed team of research analysts across multiple time zones, setting priorities, managing workloads, and ensuring timely delivery against SLAs and project timelines. Establish research best practices (source triangulation, confidence scoring, documentation standards, audit trails, and escalation paths) to ensure consistency, repeatability, and defensibility of outputs. Guide analysts on data sources and collection strategies, including how to select, evaluate, and triangulate sources to validate supplier relationships and trading activity. Implement quality assurance (QA) and continuous improvement, including regular calibration sessions, spot checks, root cause reviews of defects, and coaching to reduce rework and improve accuracy over time. Collaborate cross functionally with operations, product/development, and commercial teams to align research outputs with platform requirements, client needs, and go to market messaging. Identify new research opportunities that expand coverage and support business growth. Support customer facing engagements as needed, including methodology discussions, research readouts, and responding to client inquiries regarding data provenance and validation logic. What We're Looking For: Basic Required Qualifications: Bachelor's degree in Business, Engineering, Supply Chain Management or a related field. 5+ years of experience in research management, competitive intelligence, supply chain research, or a related role-preferably tied to automotive or global supply chains. Proven experience managing distributed teams (multiple time zones), including performance management, coaching, and operational execution. Demonstrated ability to design research methods and translate ambiguous questions into structured workflows, measurable outputs, and clear analyst instructions. Excellent written and verbal communication skills, including the ability to present research findings and defend methodology to internal and external stakeholders. Additional Preferred Qualifications: Strong understanding of automotive supply chain structures and/or procurement processes (supplier tiers, sourcing, localization, capacity constraints, and operational risk concepts). Domain expertise in Electronics & Semiconductor Systems, Powertrain & Chassis Systems, or Interior & Cabin Systems. Experience partnering with technical teams to operationalise research outputs into scalable datasets. Background in supplier discovery/validation using a mix of primary/secondary research (e.g., interviews, industry publications, trade data, corporate filings, customs/shipping signals). Experience building or managing quality programs (QA frameworks, rubrics, confidence scoring, SOPs, training curricula). Track record of publishing research (reports, briefings, client deliverables) or presenting insights to procurement, supply chain, risk, or executive audiences. Familiarity with global trade and compliance concepts relevant to automotive sourcing (e.g., sanctions/export controls exposure, country of origin considerations, forced labor screening workflows). Master's degree (MBA or related) is a plus. Compensation/Benefits Information: (This section is only applicable to US candidates) S&P Global states that the anticipated base salary range for this position is $91,805 to $181,560. Final base salary for this role will be based on the individual's geographic location, as well as experience level, skill set, training, licenses and certifications. In addition to base compensation, this role is eligible for an annual incentive plan. This role is not eligible for additional compensation such as an annual incentive bonus or sales commission plan. This role is eligible to receive additional S&P Global benefits. For more information on the benefits we provide to our employees, please click Here About S&P Global Mobility At S&P Global Mobility, we provide invaluable insights derived from unmatched automotive data, enabling our customers to anticipate change and make decisions with conviction. Our expertise helps them to optimise their businesses, reach the right consumers, and shape the future of mobility. We open the door to automotive innovation, revealing the buying patterns of today and helping customers plan for the emerging technologies of tomorrow. What's In It For You? Our Mission: Advancing Essential Intelligence. Our People: We're more than 35,000 strong worldwide-so we're able to understand nuances while having a broad perspective. Our team is driven by curiosity and a shared belief that Essential Intelligence can help build a more prosperous future for us all. From finding new ways to measure sustainability to analysing energy transition across the supply chain to building workflow solutions that make it easy to tap into insight and apply it. We are changing the way people see things and empowering them to make an impact on the world we live in. We're committed to a more equitable future and to helping our customers find new, sustainable ways of doing business. Join us and help create the critical insights that truly make a difference. Our Values: Integrity, Discovery, Partnership Benefits: We take care of you, so you can take care of business. We care about our people. That's why we provide everything you- and your career-need to thrive at S&P Global. Our benefits include: Health & Wellness: Health care coverage designed for the mind and body. Flexible Downtime: Generous time off helps keep you energized for your time on. Continuous Learning: Access a wealth of resources to grow your career and learn valuable new skills. Invest in Your Future: Secure your financial future through competitive pay, retirement planning, a continuing education programme with a company matched student loan contribution, and financial wellness programmes. Family Friendly Perks: It's not just about you. S&P Global has perks for your partners and little ones, too, with some best in class benefits for families. Beyond the Basics: From retail discounts to referral incentive awards-small perks can make a big difference. For more information on benefits by country visit: Global Hiring and Opportunity at S&P Global: At S&P Global, we are committed to fostering a connected and engaged workplace where all individuals have access to opportunities based on their skills, experience, and contributions. Our hiring practices emphasise fairness, transparency, and merit, ensuring that we attract and retain top talent. By valuing different perspectives and promoting a culture of respect and collaboration, we drive innovation and power global markets. Recruitment Fraud Alert: If you receive an email from a domain or any other regionally based domains, it is a scam and should be reported to . S&P Global never requires any candidate to pay money for job applications, interviews, offer letters, "pre employment training" or for equipment/delivery of equipment. Stay informed and protect yourself from recruitment fraud by reviewing our guidelines, fraudulent domains, and how to report suspicious activity here. Equal Opportunity Employer S&P Global is an equal opportunity employer and all qualified candidates will receive consideration for employment without regard to race/ethnicity, colour, religion, sex, sexual orientation, gender identity, national origin, age, disability, marital status, military veteran status, unemployment status, or any other status protected by law. Only electronic job submissions will be considered for employment. If you need an accommodation during the application process due to a disability, please send an email to: and your request will be forwarded to the appropriate person. US Candidates Only: The EEO is the Law Poster describes discrimination protections under federal law. Pay Transparency Nondiscrimination Provision - English_formattedESQA508c.pdf RESECH103.2 - Middle Management Tier II (EEO Job Group) Job ID: 326237 Posted On: 2026-03-06 Location: Virtual, United Kingdom
Job Description QC Lab Manager Petersfield 8.15am - 4.30pm Monday - Friday JOB REQUIREMENTS & QUALIFICATIONS Minimum Education level: Batchelor's science degree or equivalent experience Five years' laboratory experience, with at least three years in a supervisory position, preferably in microbiology, analytical chemistry or product evaluation laboratories in Quality Control for a global consumer goods or pharmaceutical company Experience in developing laboratory SOPs and revisions according to regulatory guidelines. Effective oral and written communication skills and ability to appropriately communicate information to cross functional stakeholders and suppliers Strong knowledge of GMP, ISO and safety guidelines Strong problem-solving skills Knowledge of statistical assessments of data Solid knowledge of all laboratory equipment (e.g., Viscometer, ACS Color Computer, Vitek, Analytical Instrumentation) Proficiency in Microsoft Office Suite, Electronic QMS, and SAP systems is preferred Flexible to support off-shift work when needed. POSITION SUMMARY Support the Senior Manager, in the QC Lab for a particular shift and/or lab function in planning, organizing, implementing and controlling the daily activities of the QC laboratory to ascertain that raw materials, mass and finished goods meet internal and external specifications. Responsible for overseeing lab testing processes with ability to troubleshoot instruments and issues. Conduct and supervise all OOS investigations and reject investigations. Manage QC lab equipment, qualification protocols and reports, and administration. Participate in continuous improvement projects regionally to drive efficiencies in the lab. KEY ROLES & RESPONSIBILITIES Management of QC Lab Testing for a shift or lab function Plan, organise, implement and control the daily activities of the QC laboratory to ascertain that both raw materials and assay of finished goods / mass meet internal and external specification. This includes management for lab workflow, sample analysis, sample retention, standards management, raw material qualification, TPM testing, outsourced testing, inventory management and document management Ensure execution of data integrity checks / verifications per procedures Provide QC expertise to plant hygiene program and lead corrective action based on findings. Ensure there is testing support in relation to the environmental monitoring program and any associated risk assessments Identify SOPs and support the Senior Manager, QC Lab in work instruction updates or creating new based on lab trends and CAPAs. Review SOPs and work instructions and provide to QC Lab Lead for approval. Review and trending of OOS, CAPAs and deviations related to their QC lab function Testing Data Review and Release -Data Reviewer role responsibilities Review routine supporting test data and results, including sample preparation records, chromatograms / graphs, logbooks, calculations, and data sheets. Enter results in SAP/LIMS. Release raw materials, non-OTC mass, and Cosmetic FGs in SAP Review non-routine supporting test data and results (i.e. micro testing for water systems, validation testing) Equipment Program Manage QC lab equipment budget, equipment purchases, installation and initiate change control as needed Develop lab equipment qualification (IQ/OQ/PQ) protocols and reports Manage specific area's equipment administration, including calibration, preventive maintenance, and troubleshooting as needed Compliance / Continuous Improvement within Lab Function Area Ensure all lab processes are adhering to relevant regulatory GMPs and global company policies & procedures Participate in internal audits to ensure regulatory readiness Work collaboratively with Planning, GBSC, QA Labs, Manufacturing, Validation, and Operations to drive continuous improvement. Monitor lab KPIs and drive improvements Ensure all customer complaints are investigated, improvements implemented and response made in a timely manner Support Plant and Global programmes to ensure compliance in key areas including Good Manufacturing Practices, Data Integrity, and the General Data Protection Regulation (GDPR). Personnel Management & Training Apply QC Lab objectives to their lab function area and conduct performance reviews against those objectives. Provide the coaching, mentorship and training necessary to support ongoing personal and professional development of QC lab staff (GMP and refresher training) Assist in the development and execution of quality training curriculum for the laboratory.
Mar 16, 2026
Full time
Job Description QC Lab Manager Petersfield 8.15am - 4.30pm Monday - Friday JOB REQUIREMENTS & QUALIFICATIONS Minimum Education level: Batchelor's science degree or equivalent experience Five years' laboratory experience, with at least three years in a supervisory position, preferably in microbiology, analytical chemistry or product evaluation laboratories in Quality Control for a global consumer goods or pharmaceutical company Experience in developing laboratory SOPs and revisions according to regulatory guidelines. Effective oral and written communication skills and ability to appropriately communicate information to cross functional stakeholders and suppliers Strong knowledge of GMP, ISO and safety guidelines Strong problem-solving skills Knowledge of statistical assessments of data Solid knowledge of all laboratory equipment (e.g., Viscometer, ACS Color Computer, Vitek, Analytical Instrumentation) Proficiency in Microsoft Office Suite, Electronic QMS, and SAP systems is preferred Flexible to support off-shift work when needed. POSITION SUMMARY Support the Senior Manager, in the QC Lab for a particular shift and/or lab function in planning, organizing, implementing and controlling the daily activities of the QC laboratory to ascertain that raw materials, mass and finished goods meet internal and external specifications. Responsible for overseeing lab testing processes with ability to troubleshoot instruments and issues. Conduct and supervise all OOS investigations and reject investigations. Manage QC lab equipment, qualification protocols and reports, and administration. Participate in continuous improvement projects regionally to drive efficiencies in the lab. KEY ROLES & RESPONSIBILITIES Management of QC Lab Testing for a shift or lab function Plan, organise, implement and control the daily activities of the QC laboratory to ascertain that both raw materials and assay of finished goods / mass meet internal and external specification. This includes management for lab workflow, sample analysis, sample retention, standards management, raw material qualification, TPM testing, outsourced testing, inventory management and document management Ensure execution of data integrity checks / verifications per procedures Provide QC expertise to plant hygiene program and lead corrective action based on findings. Ensure there is testing support in relation to the environmental monitoring program and any associated risk assessments Identify SOPs and support the Senior Manager, QC Lab in work instruction updates or creating new based on lab trends and CAPAs. Review SOPs and work instructions and provide to QC Lab Lead for approval. Review and trending of OOS, CAPAs and deviations related to their QC lab function Testing Data Review and Release -Data Reviewer role responsibilities Review routine supporting test data and results, including sample preparation records, chromatograms / graphs, logbooks, calculations, and data sheets. Enter results in SAP/LIMS. Release raw materials, non-OTC mass, and Cosmetic FGs in SAP Review non-routine supporting test data and results (i.e. micro testing for water systems, validation testing) Equipment Program Manage QC lab equipment budget, equipment purchases, installation and initiate change control as needed Develop lab equipment qualification (IQ/OQ/PQ) protocols and reports Manage specific area's equipment administration, including calibration, preventive maintenance, and troubleshooting as needed Compliance / Continuous Improvement within Lab Function Area Ensure all lab processes are adhering to relevant regulatory GMPs and global company policies & procedures Participate in internal audits to ensure regulatory readiness Work collaboratively with Planning, GBSC, QA Labs, Manufacturing, Validation, and Operations to drive continuous improvement. Monitor lab KPIs and drive improvements Ensure all customer complaints are investigated, improvements implemented and response made in a timely manner Support Plant and Global programmes to ensure compliance in key areas including Good Manufacturing Practices, Data Integrity, and the General Data Protection Regulation (GDPR). Personnel Management & Training Apply QC Lab objectives to their lab function area and conduct performance reviews against those objectives. Provide the coaching, mentorship and training necessary to support ongoing personal and professional development of QC lab staff (GMP and refresher training) Assist in the development and execution of quality training curriculum for the laboratory.
Computer Science Teacher £150 - £220 per day St Neots Are you an innovator ready to inspire the next generation of software engineers, cybersecurity experts, and digital architects? Can you transform complex syntax into creative solutions and make the logic of algorithms resonate with a diverse classroom? We are seeking a forward-thinking Qualified Computer Science Teacher to join a vibrant Secondary School in St Neots . This is a full-time, long-term position for a practitioner who is passionate about the evolving digital landscape and can deliver high-quality instruction across Key Stages 3, 4, and 5. Whether it's coding in Python or deconstructing network architecture, we need a teacher who can bridge the gap between theory and real-world application. Your Responsibilities Curriculum Innovation: Plan and deliver a robust Computer Science curriculum that covers programming, data representation, computer systems, and the ethical impact of technology. Programming Excellence: Guide students through practical coding challenges, primarily in Python , ensuring they develop strong computational thinking and debugging skills. Examination Success: Lead GCSE and A-Level cohorts through their specifications (OCR/AQA), providing the targeted intervention needed to secure top-tier results. Project-Based Learning: Oversee the Non-Exam Assessment (NEA) for older students, mentoring them as they design, develop, and test original software projects. Digital Citizenship: Foster an understanding of cybersecurity and online safety, equipping students with the tools to navigate the modern world responsibly. Departmental Growth: Collaborate with the wider STEM team to integrate technology across the school and lead extracurricular coding clubs or robotics challenges. What You'll Bring to the Team Qualified Teacher Status (QTS): This is mandatory for this role. Subject Expertise: A degree in Computer Science, ICT, or a related field, with a deep understanding of hardware, software, and logic. Technical Proficiency: Strong hands-on skills in at least one high-level programming language (Python preferred). Adaptable Pedagogy: The ability to differentiate complex technical concepts for students of all abilities, from digital beginners to advanced coders. Compliance: An enhanced Child DBS on the Update Service (or a willingness to process one through Randstad). Why Partner with Randstad? Elite Daily Rates: £150 - £220 per day Local Stability: Secure a consistent, full-time role in a well-regarded St Neots school. Professional Growth: Access free, certified CPD in Safeguarding, Pedagogy, and the latest classroom technologies. Dedicated Consultant: Work with Neeraj , your personal consultant who specialises in the Cambridgeshire and St Neots education markets. Referral Scheme: Earn a £300 voucher for every qualified teacher you refer who joins the Randstad team! How to Apply If you are a dedicated and supportive individual ready to make a difference in a school setting, please apply immediately with your CV or contact Neeraj at for more information. We are the UK market leader for recruitment in education. We have nearly two decades of experience helping teachers and support staff find temporary and permanent roles in schools, colleges, and nurseries. We partner with over 2,500 schools each week, supporting more than 135,000 children every day across the country, which allows us to find the right match for your skills.
Mar 16, 2026
Seasonal
Computer Science Teacher £150 - £220 per day St Neots Are you an innovator ready to inspire the next generation of software engineers, cybersecurity experts, and digital architects? Can you transform complex syntax into creative solutions and make the logic of algorithms resonate with a diverse classroom? We are seeking a forward-thinking Qualified Computer Science Teacher to join a vibrant Secondary School in St Neots . This is a full-time, long-term position for a practitioner who is passionate about the evolving digital landscape and can deliver high-quality instruction across Key Stages 3, 4, and 5. Whether it's coding in Python or deconstructing network architecture, we need a teacher who can bridge the gap between theory and real-world application. Your Responsibilities Curriculum Innovation: Plan and deliver a robust Computer Science curriculum that covers programming, data representation, computer systems, and the ethical impact of technology. Programming Excellence: Guide students through practical coding challenges, primarily in Python , ensuring they develop strong computational thinking and debugging skills. Examination Success: Lead GCSE and A-Level cohorts through their specifications (OCR/AQA), providing the targeted intervention needed to secure top-tier results. Project-Based Learning: Oversee the Non-Exam Assessment (NEA) for older students, mentoring them as they design, develop, and test original software projects. Digital Citizenship: Foster an understanding of cybersecurity and online safety, equipping students with the tools to navigate the modern world responsibly. Departmental Growth: Collaborate with the wider STEM team to integrate technology across the school and lead extracurricular coding clubs or robotics challenges. What You'll Bring to the Team Qualified Teacher Status (QTS): This is mandatory for this role. Subject Expertise: A degree in Computer Science, ICT, or a related field, with a deep understanding of hardware, software, and logic. Technical Proficiency: Strong hands-on skills in at least one high-level programming language (Python preferred). Adaptable Pedagogy: The ability to differentiate complex technical concepts for students of all abilities, from digital beginners to advanced coders. Compliance: An enhanced Child DBS on the Update Service (or a willingness to process one through Randstad). Why Partner with Randstad? Elite Daily Rates: £150 - £220 per day Local Stability: Secure a consistent, full-time role in a well-regarded St Neots school. Professional Growth: Access free, certified CPD in Safeguarding, Pedagogy, and the latest classroom technologies. Dedicated Consultant: Work with Neeraj , your personal consultant who specialises in the Cambridgeshire and St Neots education markets. Referral Scheme: Earn a £300 voucher for every qualified teacher you refer who joins the Randstad team! How to Apply If you are a dedicated and supportive individual ready to make a difference in a school setting, please apply immediately with your CV or contact Neeraj at for more information. We are the UK market leader for recruitment in education. We have nearly two decades of experience helping teachers and support staff find temporary and permanent roles in schools, colleges, and nurseries. We partner with over 2,500 schools each week, supporting more than 135,000 children every day across the country, which allows us to find the right match for your skills.
Unternehmensgruppe Theo Müller
Minsterley, Shropshire
A leading dairy company is seeking a QA Food Science Specialist to be the scientific expert across its UK sites in Market Drayton. The role focuses on maintaining food safety, quality compliance, and driving continuous improvement. Candidates should have a science-based degree in Food Science or related field, strong experience in food manufacturing, preferably with microbiology expertise. The company offers various benefits including private healthcare, pension, and generous annual leave.
Mar 16, 2026
Full time
A leading dairy company is seeking a QA Food Science Specialist to be the scientific expert across its UK sites in Market Drayton. The role focuses on maintaining food safety, quality compliance, and driving continuous improvement. Candidates should have a science-based degree in Food Science or related field, strong experience in food manufacturing, preferably with microbiology expertise. The company offers various benefits including private healthcare, pension, and generous annual leave.
Unternehmensgruppe Theo Müller
Market Drayton, Shropshire
Who we are We're Müller UK & Ireland, a family run dairy business and we're experts at what we do. Dairy is a key part of a healthy and balanced diet and we're super proud to help meet the nutritional needs of millions of people, every, single, day. To do this, our business has been split into two areas: Müller Milk & Ingredients (MMI) and Müller Yogurt & Desserts (MYD). We know that sounds like a lot, but that's why we need you! Yogurts and desserts flow through everything at Müller - from farm to factory to fridge. But the true impact comes from our people, in each and every corner of the business, working hard and as a team to put smiles on faces everywhere, making each day delicious for our shoppers. And, as the UK's most popular dairy brand, we're always striving to make a real difference for our planet, our partners and our people, putting sustainability at the heart of everything we do. Did you know that 29 Müller yogurt and desserts are eaten every second? And that's just the start, with ambitious plans to grow, while continuing to make a real difference for the planet, our partners and people, we're looking for a team of fridge fillers and self starters to help us on our mission to put a smile on the nation's face. Join a team of fridge fillers and self starters just doing their for the bigger picture. QA Food Science Specialist Location: Market Drayton, Telford or Minsterley (with travel required to all three sites) At Müller, we're driven by quality, innovation and a passion for great tasting dairy. As part of our Quality Assurance team within Müller Yogurt & Desserts, we're now looking for a QA Food Science Specialist to act as the scientific subject matter expert across our UK sites. This is a key technical role, providing leadership across microbiology, chemistry and process science, ensuring robust standards that protect food safety, quality and compliance while supporting continuous improvement. What you'll be doing: Acting as the scientific expert across Müller Yogurt & Desserts, covering the microbiological, chemicaland physical properties of food. Leading the development, deployment and governance of science based technical standards and specifications Driving spoilage prevention, mould and pathogen reduction through data led improvement plans Supporting root cause analysis of quality incidents and contributing to crisis and incident management Driving continuous improvement in laboratory quality systems, equipment capability and horizon scanning for new technologies Partnering cross functionally with Operations, Engineering, Group Quality and external laboratories Coaching and developing laboratory and site teams to strengthen quality capability at every level What we're looking for: A science based degree in Food Science, Microbiology or a related discipline Strong experience within food manufacturing, ideally FMCG or dairy and with a microbiology bias HACCP Level 4 and Food Safety Level 4 desirable but not essential A structured, analytical approach with the confidence to challenge the status quo Excellent stakeholder management and communication skills What you'll receive: In return for your commitment, drive and enthusiasm, we offer our employees numerous benefits as part of your employment, including: Private medical healthcare Contributory pension plan Life assurance Employee Assistance Programme Generous annual leave increasing with service. In addition, our employees have access to a Rewards Benefits Programme, giving you a range of discounts across 800 retailers online and in store. Why Müller? You'll be joining a business that invests in quality, technology and people, offering the opportunity to influence standards at scale while continuing to develop your technical expertise within a market leading FMCG environment.
Mar 16, 2026
Full time
Who we are We're Müller UK & Ireland, a family run dairy business and we're experts at what we do. Dairy is a key part of a healthy and balanced diet and we're super proud to help meet the nutritional needs of millions of people, every, single, day. To do this, our business has been split into two areas: Müller Milk & Ingredients (MMI) and Müller Yogurt & Desserts (MYD). We know that sounds like a lot, but that's why we need you! Yogurts and desserts flow through everything at Müller - from farm to factory to fridge. But the true impact comes from our people, in each and every corner of the business, working hard and as a team to put smiles on faces everywhere, making each day delicious for our shoppers. And, as the UK's most popular dairy brand, we're always striving to make a real difference for our planet, our partners and our people, putting sustainability at the heart of everything we do. Did you know that 29 Müller yogurt and desserts are eaten every second? And that's just the start, with ambitious plans to grow, while continuing to make a real difference for the planet, our partners and people, we're looking for a team of fridge fillers and self starters to help us on our mission to put a smile on the nation's face. Join a team of fridge fillers and self starters just doing their for the bigger picture. QA Food Science Specialist Location: Market Drayton, Telford or Minsterley (with travel required to all three sites) At Müller, we're driven by quality, innovation and a passion for great tasting dairy. As part of our Quality Assurance team within Müller Yogurt & Desserts, we're now looking for a QA Food Science Specialist to act as the scientific subject matter expert across our UK sites. This is a key technical role, providing leadership across microbiology, chemistry and process science, ensuring robust standards that protect food safety, quality and compliance while supporting continuous improvement. What you'll be doing: Acting as the scientific expert across Müller Yogurt & Desserts, covering the microbiological, chemicaland physical properties of food. Leading the development, deployment and governance of science based technical standards and specifications Driving spoilage prevention, mould and pathogen reduction through data led improvement plans Supporting root cause analysis of quality incidents and contributing to crisis and incident management Driving continuous improvement in laboratory quality systems, equipment capability and horizon scanning for new technologies Partnering cross functionally with Operations, Engineering, Group Quality and external laboratories Coaching and developing laboratory and site teams to strengthen quality capability at every level What we're looking for: A science based degree in Food Science, Microbiology or a related discipline Strong experience within food manufacturing, ideally FMCG or dairy and with a microbiology bias HACCP Level 4 and Food Safety Level 4 desirable but not essential A structured, analytical approach with the confidence to challenge the status quo Excellent stakeholder management and communication skills What you'll receive: In return for your commitment, drive and enthusiasm, we offer our employees numerous benefits as part of your employment, including: Private medical healthcare Contributory pension plan Life assurance Employee Assistance Programme Generous annual leave increasing with service. In addition, our employees have access to a Rewards Benefits Programme, giving you a range of discounts across 800 retailers online and in store. Why Müller? You'll be joining a business that invests in quality, technology and people, offering the opportunity to influence standards at scale while continuing to develop your technical expertise within a market leading FMCG environment.
Unternehmensgruppe Theo Müller
Market Drayton, Shropshire
A leading dairy company is seeking a QA Food Science Specialist to be the scientific expert across its UK sites in Market Drayton. The role focuses on maintaining food safety, quality compliance, and driving continuous improvement. Candidates should have a science-based degree in Food Science or related field, strong experience in food manufacturing, preferably with microbiology expertise. The company offers various benefits including private healthcare, pension, and generous annual leave.
Mar 16, 2026
Full time
A leading dairy company is seeking a QA Food Science Specialist to be the scientific expert across its UK sites in Market Drayton. The role focuses on maintaining food safety, quality compliance, and driving continuous improvement. Candidates should have a science-based degree in Food Science or related field, strong experience in food manufacturing, preferably with microbiology expertise. The company offers various benefits including private healthcare, pension, and generous annual leave.
We are seeking a highly experienced SCADA Commissioning Consultant to manage and coordinate SCADA commissioning activities on-site for large-scale infrastructure and energy projects. This role requires expertise in Hitachi MicroSCADA, Substation Control Systems, and grid compliance. The consultant will work closely with contractors, project managers, and stakeholders to ensure smooth execution and compliance with governance and industry standards. Key Qualifications: 5+ years of hands-on SCADA commissioning experience in large-scale energy or infrastructure projects. In-depth knowledge of Hitachi MicroSCADA, Substation Control Systems, and National Grid compliance processes. Strong technical background (B.Sc. or equivalent in Electrical Engineering or related field). Familiarity with Ørsted's governance, documentation standards, and EPC delivery model. Experience with IPMA B/C, PMP, or similar project management frameworks is desirable. Proven ability to manage contractors and lead commissioning activities independently. Key Responsibilities: Lead SCADA commissioning activities on-site, ensuring quality and timely delivery. Supervise and manage SCADA contractors, ensuring adherence to quality standards and safety regulations. Draft, maintain, and update the SCADA Commissioning Plan, defining scope, QA/QC, and timelines. Sign off on contractor checklists and commissioning documentation, ensuring accuracy and compliance. Manage and close snag lists, driving corrective actions and ensuring issues are resolved on time. Provide structured progress reports to the SCADA Package Manager and Commissioning Manager. Ensure compliance with National Grid's requirements and grid code obligations during commissioning. Coordinate with SCADA contractors, Electrical Commissioning Managers, and other stakeholders to align with the overall commissioning plan. Resolve commissioning issues independently and elevate critical matters as needed.
Mar 16, 2026
Full time
We are seeking a highly experienced SCADA Commissioning Consultant to manage and coordinate SCADA commissioning activities on-site for large-scale infrastructure and energy projects. This role requires expertise in Hitachi MicroSCADA, Substation Control Systems, and grid compliance. The consultant will work closely with contractors, project managers, and stakeholders to ensure smooth execution and compliance with governance and industry standards. Key Qualifications: 5+ years of hands-on SCADA commissioning experience in large-scale energy or infrastructure projects. In-depth knowledge of Hitachi MicroSCADA, Substation Control Systems, and National Grid compliance processes. Strong technical background (B.Sc. or equivalent in Electrical Engineering or related field). Familiarity with Ørsted's governance, documentation standards, and EPC delivery model. Experience with IPMA B/C, PMP, or similar project management frameworks is desirable. Proven ability to manage contractors and lead commissioning activities independently. Key Responsibilities: Lead SCADA commissioning activities on-site, ensuring quality and timely delivery. Supervise and manage SCADA contractors, ensuring adherence to quality standards and safety regulations. Draft, maintain, and update the SCADA Commissioning Plan, defining scope, QA/QC, and timelines. Sign off on contractor checklists and commissioning documentation, ensuring accuracy and compliance. Manage and close snag lists, driving corrective actions and ensuring issues are resolved on time. Provide structured progress reports to the SCADA Package Manager and Commissioning Manager. Ensure compliance with National Grid's requirements and grid code obligations during commissioning. Coordinate with SCADA contractors, Electrical Commissioning Managers, and other stakeholders to align with the overall commissioning plan. Resolve commissioning issues independently and elevate critical matters as needed.
Overview Every day, Imagine Communications delivers billions of media moments all over the world -anywhere, anytime and on any device. Imagine Communications delivers innovative, end-to-end media software and networking solutions to over 3,000 customers in more than 185 countries, including the top broadcast facilities and the most technologically advanced sports and live-event venues. Why Imagine? Imagine Communications offers a generous pension to all our employees, private Medical and Dental. We like to make sure all our employees are safe when travelling so we've got travel insurance covered too. Employee Wellbeing is a priority for us, so all employees and their family have access to our EAP service. We have subsidised Gym membership, Life assurance and Group income protection. A Bit About The Role Imagine Communications is seeking a Senior Software Engineer with deep C++ expertise to join our engineering team in Toronto, Canada or Cambridge, UK (both locations are remote friendly). This role focuses on high-performance development for real-time broadcast and media processing systems. The successful candidate will design, implement, optimize and maintain high-bandwidth stream processing microservices that demand high CPU, memory and network stack efficiency, within an existing microservices framework, while collaborating closely with cross-functional teams. Design, develop, and maintain high-performance backend components in modern C++. Implement and optimize real-time stream processing microservices within an existing microservice framework to deliver high bandwidth, low latency media processing. Analyze and improve CPU utilization, memory usage, network stack and kernel interactions and overall system performance. Profile and troubleshoot complex C++ applications to identify bottlenecks and inefficiencies. Develop and maintain REST-based services and interfaces. Work within Linux environments to build, debug, and deploy software solutions. Maintain and extend Bash scripting microservices orchestration layer. Collaborate with QA, DevOps, and product teams to ensure robust feature delivery. Participate in code reviews and contribute to continuous improvement of code quality and architecture. Support ongoing code maintenance, refactoring, and technical debt reduction. About You Bachelor's degree in Computer Science, Software Engineering, or equivalent experience. Senior-level experience in backend software development using modern C++. Strong expertise in multithreaded programming and concurrency concepts. Proven experience developing near real-time or high-performance systems. Solid understanding of CPU performance, memory management, Linux scheduling and application profiling techniques. Hands-on experience working on real-time or near real-time processing in Linux environments. Experience implementing or consuming REST APIs (Microsoft C++ REST SDK or similar frameworks). Strong knowledge of TCP/IP networking fundamentals. Excellent debugging, analytical, and problem-solving skills. Proficiency with Bash scripting. Strong communication skills and ability to work effectively in Agile teams. The following experience is considered an asset: Experience with high-performance networking: 100Gb/sec+, InfiniBand, RDMA, OFED, Ibverbs Experience in broadcast or media processing environments. Familiarity with SMPTE ST 2110, SMPTE 2022-6, playout, ingest, or transcoding technologies Familiarity with video processing technologies including FFmpeg (or similar) framework Exposure to UI or web-layer development. Celebrating difference, together stronger At Imagine Communications, we don't just accept difference - we celebrate it, we support it, and we thrive on it for the benefit of our customers, our employees, our products, and our communities. We are committed to providing an environment of mutual respect. Imagine Communications is proud to be an equal opportunity workplace and is an affirmative action employer.
Mar 15, 2026
Full time
Overview Every day, Imagine Communications delivers billions of media moments all over the world -anywhere, anytime and on any device. Imagine Communications delivers innovative, end-to-end media software and networking solutions to over 3,000 customers in more than 185 countries, including the top broadcast facilities and the most technologically advanced sports and live-event venues. Why Imagine? Imagine Communications offers a generous pension to all our employees, private Medical and Dental. We like to make sure all our employees are safe when travelling so we've got travel insurance covered too. Employee Wellbeing is a priority for us, so all employees and their family have access to our EAP service. We have subsidised Gym membership, Life assurance and Group income protection. A Bit About The Role Imagine Communications is seeking a Senior Software Engineer with deep C++ expertise to join our engineering team in Toronto, Canada or Cambridge, UK (both locations are remote friendly). This role focuses on high-performance development for real-time broadcast and media processing systems. The successful candidate will design, implement, optimize and maintain high-bandwidth stream processing microservices that demand high CPU, memory and network stack efficiency, within an existing microservices framework, while collaborating closely with cross-functional teams. Design, develop, and maintain high-performance backend components in modern C++. Implement and optimize real-time stream processing microservices within an existing microservice framework to deliver high bandwidth, low latency media processing. Analyze and improve CPU utilization, memory usage, network stack and kernel interactions and overall system performance. Profile and troubleshoot complex C++ applications to identify bottlenecks and inefficiencies. Develop and maintain REST-based services and interfaces. Work within Linux environments to build, debug, and deploy software solutions. Maintain and extend Bash scripting microservices orchestration layer. Collaborate with QA, DevOps, and product teams to ensure robust feature delivery. Participate in code reviews and contribute to continuous improvement of code quality and architecture. Support ongoing code maintenance, refactoring, and technical debt reduction. About You Bachelor's degree in Computer Science, Software Engineering, or equivalent experience. Senior-level experience in backend software development using modern C++. Strong expertise in multithreaded programming and concurrency concepts. Proven experience developing near real-time or high-performance systems. Solid understanding of CPU performance, memory management, Linux scheduling and application profiling techniques. Hands-on experience working on real-time or near real-time processing in Linux environments. Experience implementing or consuming REST APIs (Microsoft C++ REST SDK or similar frameworks). Strong knowledge of TCP/IP networking fundamentals. Excellent debugging, analytical, and problem-solving skills. Proficiency with Bash scripting. Strong communication skills and ability to work effectively in Agile teams. The following experience is considered an asset: Experience with high-performance networking: 100Gb/sec+, InfiniBand, RDMA, OFED, Ibverbs Experience in broadcast or media processing environments. Familiarity with SMPTE ST 2110, SMPTE 2022-6, playout, ingest, or transcoding technologies Familiarity with video processing technologies including FFmpeg (or similar) framework Exposure to UI or web-layer development. Celebrating difference, together stronger At Imagine Communications, we don't just accept difference - we celebrate it, we support it, and we thrive on it for the benefit of our customers, our employees, our products, and our communities. We are committed to providing an environment of mutual respect. Imagine Communications is proud to be an equal opportunity workplace and is an affirmative action employer.
SRT Marine Systems plc (SRT) is a market leader in the domain of international marine surveillance technology and systems. We are a respected, established, and an ambitious multi-national company headquartered in the UK with a global customer base. The company has a worldwide impact in the marine sector by leading the next generation of Maritime Domain Awareness technologies "MDA", products, and systems that significantly enhance security, safety, environmental protection, and sustainability. Our customers are global and range from the largest national coast guards to individual vessel owners. SRT is an exciting company where high-quality results are rewarded. We are ambitious and constantly seek to innovate in order to deliver better products and services to our customers. We strive to make SRT a rewarding and challenging place to work, where talented, hard-working individuals have the opportunity to make a real impact across the marine industry. Role overview of our Senior Software Tester As a Senior Software Tester you will work on the continued build of our Marine Domain Awareness (MDA) platform which is used to create an operational picture of maritime activity. Our systems ingest large volumes of streaming data from both satellite and terrestrial, along with other sensor sources. You will play a key role in validating the behaviour of a distributed, event-driven system operating on real-time maritime data. Testing activities include both automation and manual testing. The role of Senior Software Tester role is a hybrid working position based from our Cardiff office, you will be required to attend office 1 day per week as per the team's requirements. How We Work Sprint Work Developmenttickets move across the Jira board through the delivery workflow Tickets reaching the Test stage are assigned to a tester Testers validate functionality using a mix of automated and manual testing approaches QA Release Cycles Every six weeks, we conduct a dedicated two-week QA phase where: Testers pause normal sprint board work The focus shifts to release-wide regression testing Both manual and automated test suites are executed to validate the full platform Senior Software Tester - Responsibilities (not exhaustive): Test new features and improvements delivered during sprint cycles Design, implement, and maintain automated tests, along with the execution of manual exploratory and regression testing when required Validate message-driven workflows across distributed services Test REST API endpoints supporting CRUD operations within the system Participate in release regression cycles and help validate production-ready builds Investigate issues, reproduce defects, and provide clear bug reports Work closely with developers and product teams to clarify requirements and ensure testability Senior Software Tester - Required Skills and Experience Strong experience as a software tester or QA engineer Experience testing complex distributed systems or backend platforms Experience creating automated tests Familiarity with tools such as Postman (or similar API testing tools) Ability to write test scripts using one or more scripting languages (e.g. Python, JavaScript, Bash) Ability to understand system behaviour through logs, messages, and APIs Strong debugging and problem-solving skills Experience working within Agile / Scrum teams Familiarity with Jira or similar issue-tracking tools Company Benefits Highly Competitive Salary and Pension Hybrid Working Development opportunities SRT Marine Systems plc are an equal opportunity employer. We are committed to creating an inclusive working environment for all employees and actively encourage applications from all sectors of the community.
Mar 15, 2026
Full time
SRT Marine Systems plc (SRT) is a market leader in the domain of international marine surveillance technology and systems. We are a respected, established, and an ambitious multi-national company headquartered in the UK with a global customer base. The company has a worldwide impact in the marine sector by leading the next generation of Maritime Domain Awareness technologies "MDA", products, and systems that significantly enhance security, safety, environmental protection, and sustainability. Our customers are global and range from the largest national coast guards to individual vessel owners. SRT is an exciting company where high-quality results are rewarded. We are ambitious and constantly seek to innovate in order to deliver better products and services to our customers. We strive to make SRT a rewarding and challenging place to work, where talented, hard-working individuals have the opportunity to make a real impact across the marine industry. Role overview of our Senior Software Tester As a Senior Software Tester you will work on the continued build of our Marine Domain Awareness (MDA) platform which is used to create an operational picture of maritime activity. Our systems ingest large volumes of streaming data from both satellite and terrestrial, along with other sensor sources. You will play a key role in validating the behaviour of a distributed, event-driven system operating on real-time maritime data. Testing activities include both automation and manual testing. The role of Senior Software Tester role is a hybrid working position based from our Cardiff office, you will be required to attend office 1 day per week as per the team's requirements. How We Work Sprint Work Developmenttickets move across the Jira board through the delivery workflow Tickets reaching the Test stage are assigned to a tester Testers validate functionality using a mix of automated and manual testing approaches QA Release Cycles Every six weeks, we conduct a dedicated two-week QA phase where: Testers pause normal sprint board work The focus shifts to release-wide regression testing Both manual and automated test suites are executed to validate the full platform Senior Software Tester - Responsibilities (not exhaustive): Test new features and improvements delivered during sprint cycles Design, implement, and maintain automated tests, along with the execution of manual exploratory and regression testing when required Validate message-driven workflows across distributed services Test REST API endpoints supporting CRUD operations within the system Participate in release regression cycles and help validate production-ready builds Investigate issues, reproduce defects, and provide clear bug reports Work closely with developers and product teams to clarify requirements and ensure testability Senior Software Tester - Required Skills and Experience Strong experience as a software tester or QA engineer Experience testing complex distributed systems or backend platforms Experience creating automated tests Familiarity with tools such as Postman (or similar API testing tools) Ability to write test scripts using one or more scripting languages (e.g. Python, JavaScript, Bash) Ability to understand system behaviour through logs, messages, and APIs Strong debugging and problem-solving skills Experience working within Agile / Scrum teams Familiarity with Jira or similar issue-tracking tools Company Benefits Highly Competitive Salary and Pension Hybrid Working Development opportunities SRT Marine Systems plc are an equal opportunity employer. We are committed to creating an inclusive working environment for all employees and actively encourage applications from all sectors of the community.
A growing software business is hiring a Software Engineer to support continued growth and rising demand for its platform. Software Engineer Remote Up to 60,000 Java or Kotlin Spring Boot This is a back-end focused role, ideal for an engineer who enjoys building reliable, scalable applications and wants to work on software used by well-known customers. You will be involved in the design, development and delivery of new features, as well as improving core products in a fast-moving environment. The role is fully remote , with the option to attend the Newbury office around once a month if desired. What you will be doing Developing back-end applications using Java or Kotlin Building software with Spring Boot Designing and delivering new features Enhancing existing products and platform capability Working across the full software development lifecycle Supporting QA and UAT feedback through to release Collaborating with project, account and delivery teams to understand requirements and turn them into practical solutions Writing clean, maintainable, high-quality code What they are looking for Strong commercial experience in software engineering Good hands-on experience with Java or Kotlin Strong experience with Spring Boot A back-end development background Experience building scalable systems in a modern development environment Strong problem-solving skills and attention to detail Ability to work independently in a remote setup Nice to have Microservices experience Docker or Kubernetes RabbitMQ or other messaging tools MongoDB or other NoSQL database experience Experience in telecoms, billing or transaction-led systems Package Up to 60,000 Remote working Optional monthly office time in Newbury 24 days holiday plus birthday off Private medical Life assurance Critical illness cover Employee assistance programme Contributory pension Apply now or contact Chris Lynes at Spectrum IT Recruitment Spectrum IT Recruitment (South) Limited is acting as an Employment Agency in relation to this vacancy.
Mar 15, 2026
Full time
A growing software business is hiring a Software Engineer to support continued growth and rising demand for its platform. Software Engineer Remote Up to 60,000 Java or Kotlin Spring Boot This is a back-end focused role, ideal for an engineer who enjoys building reliable, scalable applications and wants to work on software used by well-known customers. You will be involved in the design, development and delivery of new features, as well as improving core products in a fast-moving environment. The role is fully remote , with the option to attend the Newbury office around once a month if desired. What you will be doing Developing back-end applications using Java or Kotlin Building software with Spring Boot Designing and delivering new features Enhancing existing products and platform capability Working across the full software development lifecycle Supporting QA and UAT feedback through to release Collaborating with project, account and delivery teams to understand requirements and turn them into practical solutions Writing clean, maintainable, high-quality code What they are looking for Strong commercial experience in software engineering Good hands-on experience with Java or Kotlin Strong experience with Spring Boot A back-end development background Experience building scalable systems in a modern development environment Strong problem-solving skills and attention to detail Ability to work independently in a remote setup Nice to have Microservices experience Docker or Kubernetes RabbitMQ or other messaging tools MongoDB or other NoSQL database experience Experience in telecoms, billing or transaction-led systems Package Up to 60,000 Remote working Optional monthly office time in Newbury 24 days holiday plus birthday off Private medical Life assurance Critical illness cover Employee assistance programme Contributory pension Apply now or contact Chris Lynes at Spectrum IT Recruitment Spectrum IT Recruitment (South) Limited is acting as an Employment Agency in relation to this vacancy.
A leading engineering firm in Glenrothes is seeking a QA/QC Inspector to ensure compliance with quality standards. The role includes verifying incoming goods, collaborating with the quality department, and maintaining inspection equipment. Candidates should have a recognised engineering apprenticeship and experience in medium to heavy engineering environments. This role requires excellent communication skills and familiarity with CMM and Gauge maker equipment. A competitive salary, shift work hours, and benefits package are offered.
Mar 15, 2026
Full time
A leading engineering firm in Glenrothes is seeking a QA/QC Inspector to ensure compliance with quality standards. The role includes verifying incoming goods, collaborating with the quality department, and maintaining inspection equipment. Candidates should have a recognised engineering apprenticeship and experience in medium to heavy engineering environments. This role requires excellent communication skills and familiarity with CMM and Gauge maker equipment. A competitive salary, shift work hours, and benefits package are offered.
As Modular Services Project Manager, you will oversee the end to end delivery of modular LV/MV power pods and associated electrical systems-from planning and design coordination through manufacturing, FAT, installation, and commissioning support. This role requires a strong technical background in LV/MV systems, switchgear, and panel assembly, combined with excellent project leadership, quality management, and stakeholder coordination skills. Key Responsibilities Lead and manage modular power pod projects from Sales phase through design, BIM, build, FAT, delivery, and client handover. Coordinate project activities between Sales, engineering, production, design, QA, and subcontractors. Oversee FAT processes, ensuring documentation, test procedures, and results meet ISO 9001 requirements. Monitor project timelines, budgets, resources, and risk registers. Review drawings, schematics, and layouts (GA) and ensure accurate installation and build quality. Manage quality audits, testing standards, and project reporting. Support and manage on site installation, commissioning, and resolution of technical issues to support project sign off. Maintain excellent communication with clients, suppliers, and internal teams. Promote continuous improvement across modular build and electrical testing processes. Qualifications Proven background in LV/MV switchgear, control panel wiring, or modular electrical systems. FAT testing experience, liaise with clients and company stakeholders. Experience managing electrical projects or major packages within a technical environment. Ability to interpret electrical schematics, GA drawings, and technical specifications. Strong understanding of quality processes, documentation control, and compliance. Proficient with project management software and Microsoft office applications. Experience delivering modular units, prefabricated power systems, substations, or electrical rooms. Previous leadership experience in engineering teams or project environments. Exposure to design, manufacturing, and installation of LV/MV distribution systems. Level 7 Diploma in Project Management (or equivalent industry experience). ECS Gold Card electrician. Benefits Private Health Insurance Performance Bonus 25 days annual leave + bank holidays Birthday Off Pension Plan Hybrid working / Flexible working
Mar 15, 2026
Full time
As Modular Services Project Manager, you will oversee the end to end delivery of modular LV/MV power pods and associated electrical systems-from planning and design coordination through manufacturing, FAT, installation, and commissioning support. This role requires a strong technical background in LV/MV systems, switchgear, and panel assembly, combined with excellent project leadership, quality management, and stakeholder coordination skills. Key Responsibilities Lead and manage modular power pod projects from Sales phase through design, BIM, build, FAT, delivery, and client handover. Coordinate project activities between Sales, engineering, production, design, QA, and subcontractors. Oversee FAT processes, ensuring documentation, test procedures, and results meet ISO 9001 requirements. Monitor project timelines, budgets, resources, and risk registers. Review drawings, schematics, and layouts (GA) and ensure accurate installation and build quality. Manage quality audits, testing standards, and project reporting. Support and manage on site installation, commissioning, and resolution of technical issues to support project sign off. Maintain excellent communication with clients, suppliers, and internal teams. Promote continuous improvement across modular build and electrical testing processes. Qualifications Proven background in LV/MV switchgear, control panel wiring, or modular electrical systems. FAT testing experience, liaise with clients and company stakeholders. Experience managing electrical projects or major packages within a technical environment. Ability to interpret electrical schematics, GA drawings, and technical specifications. Strong understanding of quality processes, documentation control, and compliance. Proficient with project management software and Microsoft office applications. Experience delivering modular units, prefabricated power systems, substations, or electrical rooms. Previous leadership experience in engineering teams or project environments. Exposure to design, manufacturing, and installation of LV/MV distribution systems. Level 7 Diploma in Project Management (or equivalent industry experience). ECS Gold Card electrician. Benefits Private Health Insurance Performance Bonus 25 days annual leave + bank holidays Birthday Off Pension Plan Hybrid working / Flexible working
MANUFACTURING SUPERVISOR Job Title Manufacturing Supervisor Location St Albans, Hertfordshire Salary £42,000 £45,000 Shift Monday to Friday (8am 4pm) Job Role of the Manufacturing Supervisor. A fantastic opportunity has arisen for an experienced Manufacturing Supervisor to join a well-established UK pharmaceutical manufacturer operating from a modern, state-of-the-art GMP facility in Hertfordshire. Following continued growth and internal movement, the company is looking to strengthen its manufacturing leadership team with a motivated and hands-on supervisor. In this role, you will report directly to the Manufacturing Manager and lead a manufacturing team of approximately 15 operators. You will be responsible for overseeing daily production activities while ensuring high standards of quality, compliance, safety, and operational efficiency. The successful candidate will also deputise for the Manufacturing Manager when required. You will coordinate day-to-day manufacturing operations including blending, granulation, compression, and encapsulation processes, ensuring all activities are completed in line with cGMP, SOPs, MHRA requirements, approved batch records, and site safety procedures. The position also involves monitoring production performance, managing workflow, and supporting continuous improvement initiatives across the manufacturing department. Sector Pharmaceutical Manufacturing Non-Negotiable Requirements of the Manufacturing Supervisor Supervisory or leadership experience within a pharmaceutical or GMP-regulated manufacturing environment. Requirements for the Manufacturing Supervisor. Experience leading and developing production teams within a regulated manufacturing environment. Strong understanding of cGMP standards, SOPs, and MHRA requirements. Experience managing deviations, investigations, and CAPA processes. Confident communication, leadership, and team management skills. Desirable Requirements for the Manufacturing Supervisor. Engineering or pharmaceutical qualification (Level 3 or equivalent). Experience supporting audits and cross-functional collaboration with QA, QC, Engineering, and Production Planning teams. The Manufacturing Supervisor will benefit from: Working for a stable and well-established pharmaceutical manufacturer. Competitive salary package of £42,000 £45,000 depending on experience. Monday to Friday working hours (8am 4pm) supporting work-life balance. 28 days holiday (inclusive), pension scheme, and bonus opportunities. Long-term career progression within a growing GMP manufacturing environment. If you are interested in this role and feel that you have the right skills, then please click apply at the bottom of this advert. For further details contact Consultant Name at Pioneer Selection. As a registered candidate with Pioneer Selection Ltd, you automatically become eligible for our referral scheme. You will receive £250 for every candidate we place in permanent employment who has been recommended by you. Terms and Conditions apply please see our website for further details.
Mar 15, 2026
Full time
MANUFACTURING SUPERVISOR Job Title Manufacturing Supervisor Location St Albans, Hertfordshire Salary £42,000 £45,000 Shift Monday to Friday (8am 4pm) Job Role of the Manufacturing Supervisor. A fantastic opportunity has arisen for an experienced Manufacturing Supervisor to join a well-established UK pharmaceutical manufacturer operating from a modern, state-of-the-art GMP facility in Hertfordshire. Following continued growth and internal movement, the company is looking to strengthen its manufacturing leadership team with a motivated and hands-on supervisor. In this role, you will report directly to the Manufacturing Manager and lead a manufacturing team of approximately 15 operators. You will be responsible for overseeing daily production activities while ensuring high standards of quality, compliance, safety, and operational efficiency. The successful candidate will also deputise for the Manufacturing Manager when required. You will coordinate day-to-day manufacturing operations including blending, granulation, compression, and encapsulation processes, ensuring all activities are completed in line with cGMP, SOPs, MHRA requirements, approved batch records, and site safety procedures. The position also involves monitoring production performance, managing workflow, and supporting continuous improvement initiatives across the manufacturing department. Sector Pharmaceutical Manufacturing Non-Negotiable Requirements of the Manufacturing Supervisor Supervisory or leadership experience within a pharmaceutical or GMP-regulated manufacturing environment. Requirements for the Manufacturing Supervisor. Experience leading and developing production teams within a regulated manufacturing environment. Strong understanding of cGMP standards, SOPs, and MHRA requirements. Experience managing deviations, investigations, and CAPA processes. Confident communication, leadership, and team management skills. Desirable Requirements for the Manufacturing Supervisor. Engineering or pharmaceutical qualification (Level 3 or equivalent). Experience supporting audits and cross-functional collaboration with QA, QC, Engineering, and Production Planning teams. The Manufacturing Supervisor will benefit from: Working for a stable and well-established pharmaceutical manufacturer. Competitive salary package of £42,000 £45,000 depending on experience. Monday to Friday working hours (8am 4pm) supporting work-life balance. 28 days holiday (inclusive), pension scheme, and bonus opportunities. Long-term career progression within a growing GMP manufacturing environment. If you are interested in this role and feel that you have the right skills, then please click apply at the bottom of this advert. For further details contact Consultant Name at Pioneer Selection. As a registered candidate with Pioneer Selection Ltd, you automatically become eligible for our referral scheme. You will receive £250 for every candidate we place in permanent employment who has been recommended by you. Terms and Conditions apply please see our website for further details.
At OQC, we're building the quantum computers that will power the next generation of scientific discovery and commercial innovation. Our mission is to put quantum in the hands of humanity - and we're looking for exceptional engineers to help us do it. We are seeking a Senior Software Engineer to join our growing Compiler team and shape the future of our compiler stack. This is a hands on role where you will own complex technical challenges, shape architectural decisions, and mentor other engineers while applying your expertise in classical compilers to the cutting edge of quantum computing. The Role The Senior Software Engineer plays a pivotal role in designing, building and delivering the advanced software systems that underpin the production and operation of OQC's quantum computers. This role owns complex technical challenges end to end; from gathering requirements and architecting robust solutions through to prototyping, deployment and production support, ensuring software is scalable, high performance and fit for purpose in a cutting edge quantum environment. Beyond hands on engineering, the role provides technical leadership, setting direction on architecture and best practice, balancing technical risk against business progress, mentoring and up skilling other engineers, and driving high standards in quality, performance and security. This is a role for someone who not only solves deep technical problems, but shapes how those problems are approached across the organisation. What you'll be working on: Own: Lead the end to end software development lifecycle within OQC's compiler development, from requirements gathering and solution design through to deployment and production support. Architect: Design scalable, high performance software solutions to support our long term technical strategy. Prioritise: Independently set development priorities within the compiler team, balancing cross functional dependencies, resource constraints and delivery milestones. Guide: Assign tasks, mentor engineers and proactively remove blockers, ensuring technical challenges are identified early and resolved effectively. Resolve: Debug and take ownership of complex development and production issues, managing escalations and driving problems through to robust, permanent solutions. Assure: Uphold high standards in code quality, testing, documentation, security and non functional performance requirements across all deliverables. Collaborate: Partner with internal stakeholders to translate technical requirements into practical, fit for purpose solutions. Improve: Continuously evaluate tools, frameworks and industry trends, recommending and implementing improvements that strengthen engineering capability and product quality. What We're Looking For We value strong fundamentals, technical curiosity, and a passion for challenging problems. Coding skills: Extensive knowledge of Python is essential Classical Compilers: Knowledge and experience of LLVM based compiler techniques Low Level Programming Languages: Excellent knowledge of C/C++ or other low level programming languages such as Rust Solid Foundational Knowledge: Understanding of Computing Science concepts (OOAD / Code Structure, Algorithms and Data Structures, Operating Systems, Networking). Project Lifecycle Ownership: Design complex new systems from the requirements to production ideally in an agile environment. Mentoring: Proven ability to coach others in complex areas to upskill their technical performance Commitment to Quality: Knowledge of QA as applied to software and products The "Nice to Haves" Experience with Embedded software and/or working close to the hardware control systems. Knowledge or experience of signal processing Why Join OQC? At OQC, you'll work shoulder to shoulder with world class scientists, engineers and technologists who are redefining what's computationally possible. This is a rare opportunity to apply your expertise to genuinely cutting edge technology that moves beyond theory and into real world impact - solving meaningful problems across science, industry and society. If you're motivated by deep technical challenges, collaborative excellence, and the chance to help shape the future of quantum computing, OQC offers a place where your work will truly matter. Learn more about our benefits and positive work culture here: Closing date for applications: Friday 13th March
Mar 15, 2026
Full time
At OQC, we're building the quantum computers that will power the next generation of scientific discovery and commercial innovation. Our mission is to put quantum in the hands of humanity - and we're looking for exceptional engineers to help us do it. We are seeking a Senior Software Engineer to join our growing Compiler team and shape the future of our compiler stack. This is a hands on role where you will own complex technical challenges, shape architectural decisions, and mentor other engineers while applying your expertise in classical compilers to the cutting edge of quantum computing. The Role The Senior Software Engineer plays a pivotal role in designing, building and delivering the advanced software systems that underpin the production and operation of OQC's quantum computers. This role owns complex technical challenges end to end; from gathering requirements and architecting robust solutions through to prototyping, deployment and production support, ensuring software is scalable, high performance and fit for purpose in a cutting edge quantum environment. Beyond hands on engineering, the role provides technical leadership, setting direction on architecture and best practice, balancing technical risk against business progress, mentoring and up skilling other engineers, and driving high standards in quality, performance and security. This is a role for someone who not only solves deep technical problems, but shapes how those problems are approached across the organisation. What you'll be working on: Own: Lead the end to end software development lifecycle within OQC's compiler development, from requirements gathering and solution design through to deployment and production support. Architect: Design scalable, high performance software solutions to support our long term technical strategy. Prioritise: Independently set development priorities within the compiler team, balancing cross functional dependencies, resource constraints and delivery milestones. Guide: Assign tasks, mentor engineers and proactively remove blockers, ensuring technical challenges are identified early and resolved effectively. Resolve: Debug and take ownership of complex development and production issues, managing escalations and driving problems through to robust, permanent solutions. Assure: Uphold high standards in code quality, testing, documentation, security and non functional performance requirements across all deliverables. Collaborate: Partner with internal stakeholders to translate technical requirements into practical, fit for purpose solutions. Improve: Continuously evaluate tools, frameworks and industry trends, recommending and implementing improvements that strengthen engineering capability and product quality. What We're Looking For We value strong fundamentals, technical curiosity, and a passion for challenging problems. Coding skills: Extensive knowledge of Python is essential Classical Compilers: Knowledge and experience of LLVM based compiler techniques Low Level Programming Languages: Excellent knowledge of C/C++ or other low level programming languages such as Rust Solid Foundational Knowledge: Understanding of Computing Science concepts (OOAD / Code Structure, Algorithms and Data Structures, Operating Systems, Networking). Project Lifecycle Ownership: Design complex new systems from the requirements to production ideally in an agile environment. Mentoring: Proven ability to coach others in complex areas to upskill their technical performance Commitment to Quality: Knowledge of QA as applied to software and products The "Nice to Haves" Experience with Embedded software and/or working close to the hardware control systems. Knowledge or experience of signal processing Why Join OQC? At OQC, you'll work shoulder to shoulder with world class scientists, engineers and technologists who are redefining what's computationally possible. This is a rare opportunity to apply your expertise to genuinely cutting edge technology that moves beyond theory and into real world impact - solving meaningful problems across science, industry and society. If you're motivated by deep technical challenges, collaborative excellence, and the chance to help shape the future of quantum computing, OQC offers a place where your work will truly matter. Learn more about our benefits and positive work culture here: Closing date for applications: Friday 13th March
Bowel Cancer Screening - Southern Hub B3 The Royal Surrey County Hospital is seeking to appoint enthusiastic Screening Officers to join a dynamic and friendly team dedicated to the provision of a high quality screening service for the NHS Bowel Cancer Screening Hub located on the Surrey Research Park, Guildford. The NHS Bowel Cancer Screening Programme provides Bowel Cancer Screening in England, and the Southern Hub serves a population of 15.7 million in the South of England performing around 1.7 million tests per year. The Hub invites all 54-74 years olds within its population to be screened using the faecal occult blood test and we are currently extending the age range down to 50 years old. It provides a freephone helpline service, a modern laboratory and liaises with 18 screening centre in their provision of colonoscopy investigation for all participants with positive screening results. The successful candidate will be a part of the screening officer team at the Hub providing day to day support to our busy helpline and laboratory and undertaking various administrative and clerical duties to ensure we are providing a high quality service for our users. Please note this role does not meet the new UKVI requirements for sponsorship Main duties of the job The post holder will work in both the Hub laboratory and Helpline/Administrative areas. The proportion of time spent in each area will depend on the needs of the service. As the programme develops there will be opportunities for staff to develop their skills in specific areas. Be competent in the use of Bowel Cancer Screening Software (BCSS), identify population cohorts for screening and arrange for the circulation of letters, leaflets and test kits, make a computerised record of test results, and extract from the system data required for quality monitoring and reporting. Receive and respond to telephone calls from participants, relatives, members of the public and other professional's organisations using prepared guidelines in an efficient, helpful, tactful and compassionate manner. Undertake specimen reception and recording in accordance with an approved procedure As a competent member of the team, be on hand to guide, train and supervise the work of new and junior team members. About us Royal Surrey is a compassionate and collaborative acute and community Trust. Recognising that our 5000 colleagues are our greatest strength, we offer a comprehensive health and wellbeing program along with a commitment to developing and advancing your career. Our diverse and welcoming Royal Surrey family will ensure you that you feel valued from your initial interview through your entire tenure. We are clinically led and provide joined up care by bridging the gap between hospital and community services alongside regional specialist cancer care. Our main acute hospital site is in Guildford with community hospital sites at Milford, Haslemere and Cranleigh. We provide adult community health services in homes across Guildford and Waverley. The Care Quality Commission (CQC) have given us an overall rating of Outstanding. Royal Surrey has a strong reputation and history to build on. We are proud of our achievements and we are investing in our colleagues through our commitment to supporting professional development as well as investing more than £45 million in our physical environment and new equipment in the next few years. There has never been a better time to join us. Although it isn't the Trusts normal practice, adverts may close early, so you are encouraged to submit an application as soon as possible. A video about the Royal Surrey - Job responsibilities Please refer to the full Job Description Do you thrive in a role where you know youre making a positive impact? Are you looking to join a supportive and engaged team? Would you enjoy a role with true variety, blending supporting the public, laboratory and administration work? Laboratory Activities Undertake specimen reception and recording in accordance with an approved procedure. Undertake, and where directed supervise others in, quality assurance procedures including internal QC and external QA measurements. Be responsible for tidiness and cleanliness of the laboratory. Use and maintain all laboratory equipment according to Hub Standard Operating Procedures (SOPs). Use maintenance and fault reporting of the equipment within the department in compliance with Hub policies and SOPs. Support the Laboratory & Quality Lead and Team Leaders with the organisation of the department ensuring an efficient and effective service. To assist the Laboratory & Quality Lead and Team Leaders in the provision of progress and performance reports as required. Maintain within the department appropriate stock levels including reagents and stationary. Ensure safe disposal of specimens and waste in compliance with Hub SOPs. Ensure work is carried out efficiently and accurately in accordance with SOPs. Be aware of and comply at all times with the Trust, BSPS, and Hub Health and Safety regulations and safe laboratory procedures. The Hub has free parking on site and is based on the Surrey Research Park in Guildford surrounded by green spaces. The Hub building is light, spacious and close to the local amenities of the Royal Surrey Hospital. We are looking for an enthusiastic team player who is looking for a new challenge. Should you wish to discuss the role in more detail please contact Tina Cook either via email on or via phone on . Applicants are advised to visit the hub prior to applying to gain a better understanding of the role and service. Person Specification Qualifications Educated to GCSE level grade C or above or equivalent qualification or experience. Knowledge and Experience Proven experience working within an multidisciplinary office environment Proven knowledge of computers to include the use of Microsoft Office and Windows - this will be tested at interview Proven experience of working with the public Proven experience working within the NHS Bowel Screening Programme including the use of the Bowel Cancer Screening System Proven experience working within a laboratory setting Proven experience working within an NHS environment Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions. Employer name Royal Surrey NHS Foundation Trust Address Southern Royal Surrey County Hospital £26,240 to £27,928 a yearper annum including (HCAS) High Cost Area Supplement Contract Permanent Working pattern Full-time Reference number 384-AR-EMF20039/40 Job locations Southern Royal Surrey County Hospital
Mar 14, 2026
Full time
Bowel Cancer Screening - Southern Hub B3 The Royal Surrey County Hospital is seeking to appoint enthusiastic Screening Officers to join a dynamic and friendly team dedicated to the provision of a high quality screening service for the NHS Bowel Cancer Screening Hub located on the Surrey Research Park, Guildford. The NHS Bowel Cancer Screening Programme provides Bowel Cancer Screening in England, and the Southern Hub serves a population of 15.7 million in the South of England performing around 1.7 million tests per year. The Hub invites all 54-74 years olds within its population to be screened using the faecal occult blood test and we are currently extending the age range down to 50 years old. It provides a freephone helpline service, a modern laboratory and liaises with 18 screening centre in their provision of colonoscopy investigation for all participants with positive screening results. The successful candidate will be a part of the screening officer team at the Hub providing day to day support to our busy helpline and laboratory and undertaking various administrative and clerical duties to ensure we are providing a high quality service for our users. Please note this role does not meet the new UKVI requirements for sponsorship Main duties of the job The post holder will work in both the Hub laboratory and Helpline/Administrative areas. The proportion of time spent in each area will depend on the needs of the service. As the programme develops there will be opportunities for staff to develop their skills in specific areas. Be competent in the use of Bowel Cancer Screening Software (BCSS), identify population cohorts for screening and arrange for the circulation of letters, leaflets and test kits, make a computerised record of test results, and extract from the system data required for quality monitoring and reporting. Receive and respond to telephone calls from participants, relatives, members of the public and other professional's organisations using prepared guidelines in an efficient, helpful, tactful and compassionate manner. Undertake specimen reception and recording in accordance with an approved procedure As a competent member of the team, be on hand to guide, train and supervise the work of new and junior team members. About us Royal Surrey is a compassionate and collaborative acute and community Trust. Recognising that our 5000 colleagues are our greatest strength, we offer a comprehensive health and wellbeing program along with a commitment to developing and advancing your career. Our diverse and welcoming Royal Surrey family will ensure you that you feel valued from your initial interview through your entire tenure. We are clinically led and provide joined up care by bridging the gap between hospital and community services alongside regional specialist cancer care. Our main acute hospital site is in Guildford with community hospital sites at Milford, Haslemere and Cranleigh. We provide adult community health services in homes across Guildford and Waverley. The Care Quality Commission (CQC) have given us an overall rating of Outstanding. Royal Surrey has a strong reputation and history to build on. We are proud of our achievements and we are investing in our colleagues through our commitment to supporting professional development as well as investing more than £45 million in our physical environment and new equipment in the next few years. There has never been a better time to join us. Although it isn't the Trusts normal practice, adverts may close early, so you are encouraged to submit an application as soon as possible. A video about the Royal Surrey - Job responsibilities Please refer to the full Job Description Do you thrive in a role where you know youre making a positive impact? Are you looking to join a supportive and engaged team? Would you enjoy a role with true variety, blending supporting the public, laboratory and administration work? Laboratory Activities Undertake specimen reception and recording in accordance with an approved procedure. Undertake, and where directed supervise others in, quality assurance procedures including internal QC and external QA measurements. Be responsible for tidiness and cleanliness of the laboratory. Use and maintain all laboratory equipment according to Hub Standard Operating Procedures (SOPs). Use maintenance and fault reporting of the equipment within the department in compliance with Hub policies and SOPs. Support the Laboratory & Quality Lead and Team Leaders with the organisation of the department ensuring an efficient and effective service. To assist the Laboratory & Quality Lead and Team Leaders in the provision of progress and performance reports as required. Maintain within the department appropriate stock levels including reagents and stationary. Ensure safe disposal of specimens and waste in compliance with Hub SOPs. Ensure work is carried out efficiently and accurately in accordance with SOPs. Be aware of and comply at all times with the Trust, BSPS, and Hub Health and Safety regulations and safe laboratory procedures. The Hub has free parking on site and is based on the Surrey Research Park in Guildford surrounded by green spaces. The Hub building is light, spacious and close to the local amenities of the Royal Surrey Hospital. We are looking for an enthusiastic team player who is looking for a new challenge. Should you wish to discuss the role in more detail please contact Tina Cook either via email on or via phone on . Applicants are advised to visit the hub prior to applying to gain a better understanding of the role and service. Person Specification Qualifications Educated to GCSE level grade C or above or equivalent qualification or experience. Knowledge and Experience Proven experience working within an multidisciplinary office environment Proven knowledge of computers to include the use of Microsoft Office and Windows - this will be tested at interview Proven experience of working with the public Proven experience working within the NHS Bowel Screening Programme including the use of the Bowel Cancer Screening System Proven experience working within a laboratory setting Proven experience working within an NHS environment Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions. Employer name Royal Surrey NHS Foundation Trust Address Southern Royal Surrey County Hospital £26,240 to £27,928 a yearper annum including (HCAS) High Cost Area Supplement Contract Permanent Working pattern Full-time Reference number 384-AR-EMF20039/40 Job locations Southern Royal Surrey County Hospital
