Job Title: QC Technician Location: Billingshurst, West Sussex Salary: 28,500 per annum Job Type: Full Time, Permanent Work Pattern: We operate to a rotating shift pattern as follows: Early shift 06:45-14:45 (Monday to Thursday) and 06:45-13:45 (Friday). Late shift 14:30-22:30 (Monday to Thursday) and 13:30-20:30 (Friday). Saturday morning shift overtime available occasionally. About us: We are a dynamic and innovative small to medium sized business, established in Billingshurst in 1973. We are one of the World's leading manufacturers of water purification and disinfection tablets, supplying government organisations, charities and prominent retailers with our lifesaving products. Our commitment to quality and sustainability drives our success, and we are looking for an additional, dedicated and detail oriented, QC Technician to join our current team of two. About the role: As a QC Technician, you will be responsible for ensuring that our products and processes meet the highest standards of quality, compliance, and customer satisfaction. Full training will be provided however experience operating in food or pharmaceutical environments would be advantageous. Key Responsibilities: Follow safety protocols and maintain a clean work environment. Check that incoming Raw Materials are within specification. Check bulk and finished goods are produced within acceptable limits of quality, quantity and efficiency. Ensure that in-process control quality meets the specification and requirement stipulated in the work instructions or procedures. Provide accurate testing of components, Raw Materials, bulk/finished products and stability samples and technical support in the Analytical QC lab. Collecting, logging and storing of QC retention samples. Monitoring and ordering lab supplies. To calibrate QC laboratory equipment as per schedule on the appropriate SOP. To be fully conversant with GMP principles and QA SOP's. Checking of Batch records ensuring in Process Control Checks are being completed, and cross checking test results made by operations. About you: Highly literate. Good level of conversational and written English Highly numerate Experience of quality control practices/environment. Previous experience in a manufacturing or production environment (pharmaceutical/food manufacture etc. preferred) Experience of GMP/FMCG environment (preferred) Strong attention to detail and problem-solving skills Organised and methodical Good communication and teamwork abilities Ability to work to deadlines Willingness to work rotating shifts and overtime as needed. What we offer: Competitive salary Overtime during busy periods Comprehensive training and support Health and wellbeing programme Free onsite parking Additional Information: If you feel you have the experience and knowledge we're looking for we would love to hear from you. Hydrachem is an equal opportunities employer. All data obtained will be handled in accordance with GDPR requirements. Please click on the APPLY button to submit your CV for this role. Candidates with experience of: Quality Technician, Quality Control Inspector, Quality Inspector, Manufacturing Quality Assurance Technician, QC Analyst, Manufacturing Quality Analyst, Production Quality Assurance Specialist, may also be considered for this role.
Aug 22, 2026
Full time
Job Title: QC Technician Location: Billingshurst, West Sussex Salary: 28,500 per annum Job Type: Full Time, Permanent Work Pattern: We operate to a rotating shift pattern as follows: Early shift 06:45-14:45 (Monday to Thursday) and 06:45-13:45 (Friday). Late shift 14:30-22:30 (Monday to Thursday) and 13:30-20:30 (Friday). Saturday morning shift overtime available occasionally. About us: We are a dynamic and innovative small to medium sized business, established in Billingshurst in 1973. We are one of the World's leading manufacturers of water purification and disinfection tablets, supplying government organisations, charities and prominent retailers with our lifesaving products. Our commitment to quality and sustainability drives our success, and we are looking for an additional, dedicated and detail oriented, QC Technician to join our current team of two. About the role: As a QC Technician, you will be responsible for ensuring that our products and processes meet the highest standards of quality, compliance, and customer satisfaction. Full training will be provided however experience operating in food or pharmaceutical environments would be advantageous. Key Responsibilities: Follow safety protocols and maintain a clean work environment. Check that incoming Raw Materials are within specification. Check bulk and finished goods are produced within acceptable limits of quality, quantity and efficiency. Ensure that in-process control quality meets the specification and requirement stipulated in the work instructions or procedures. Provide accurate testing of components, Raw Materials, bulk/finished products and stability samples and technical support in the Analytical QC lab. Collecting, logging and storing of QC retention samples. Monitoring and ordering lab supplies. To calibrate QC laboratory equipment as per schedule on the appropriate SOP. To be fully conversant with GMP principles and QA SOP's. Checking of Batch records ensuring in Process Control Checks are being completed, and cross checking test results made by operations. About you: Highly literate. Good level of conversational and written English Highly numerate Experience of quality control practices/environment. Previous experience in a manufacturing or production environment (pharmaceutical/food manufacture etc. preferred) Experience of GMP/FMCG environment (preferred) Strong attention to detail and problem-solving skills Organised and methodical Good communication and teamwork abilities Ability to work to deadlines Willingness to work rotating shifts and overtime as needed. What we offer: Competitive salary Overtime during busy periods Comprehensive training and support Health and wellbeing programme Free onsite parking Additional Information: If you feel you have the experience and knowledge we're looking for we would love to hear from you. Hydrachem is an equal opportunities employer. All data obtained will be handled in accordance with GDPR requirements. Please click on the APPLY button to submit your CV for this role. Candidates with experience of: Quality Technician, Quality Control Inspector, Quality Inspector, Manufacturing Quality Assurance Technician, QC Analyst, Manufacturing Quality Analyst, Production Quality Assurance Specialist, may also be considered for this role.
Job Title: Sanctions Supervisor/QC Department: Financial Crime Duration: 12 months (highly likely extension) Location: London (Hybrid) Working Pattern: Full Time Join Our Team Are you passionate about financial crime prevention and regulatory compliance? Our client, a leading organisation in the financial services sector, is seeking a skilled Sanctions Supervisor/QC to enhance their Customer Due Diligence (CDD) team. This is an exciting opportunity for an experienced professional to contribute to the protection of the organisation against financial crime and sanctions-related risks. Key Responsibilities Act as the subject matter expert in the first line of defence model, identifying financial crime risks during client onboarding and periodic due diligence processes. Ensure accurate completion of customer information on CDD and operational systems, validating and screening data thoroughly. Conduct quality control (QC) checks and approve the work of analysts, ensuring adherence to the organisation's standards and procedures. Produce documentation and assist in daily workflows, especially during peak business activities. Monitor the Bank's internal sanctions screening tool, ensuring timely reviews and accurate documentation for regulatory compliance. Prepare and check sanctions validation packs, conducting thorough research and analysis of client exposure to sensitive countries. Liaise with various stakeholders across departments, providing expert advice on CDD and documentation matters. Support the ongoing training and development of junior staff, fostering a collaborative team environment. Qualifications and Skills Strong understanding of financial crime, sanctions, and AML regulations. Externally recognised qualifications in AML and customer due diligence (e.g., ICA Certificates, ACAMS) preferred. Excellent communication skills, both written and verbal, with the ability to convey complex information clearly. Proven analytical skills with a keen eye for detail and accuracy in documentation and reporting. Experience in mentoring and coaching team members, providing constructive feedback in a supportive manner. Proficiency in relevant systems (e.g., LJ Jones, Moody's Orbis, FircoSoft) is desirable. Why Join Us? This role presents a unique chance to impact the organisation's financial crime prevention efforts actively. You will collaborate with a diverse team, enhancing your expertise in compliance and regulatory matters. If you are self-sufficient, proactive, and ready to take on new challenges, we encourage you to apply. We use generative AI tools to support our candidate screening process. This helps us ensure a fair, consistent, and efficient experience for all applicants. Rest assured, all final decisions are made by our hiring team, and your application will be reviewed with care and attention. Adecco is a disability-confident employer. It is important to us that we run an inclusive and accessible recruitment process to support candidates of all backgrounds and all abilities to apply. Adecco is committed to building a supportive environment for you to explore the next steps in your career. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you.
Aug 21, 2026
Contractor
Job Title: Sanctions Supervisor/QC Department: Financial Crime Duration: 12 months (highly likely extension) Location: London (Hybrid) Working Pattern: Full Time Join Our Team Are you passionate about financial crime prevention and regulatory compliance? Our client, a leading organisation in the financial services sector, is seeking a skilled Sanctions Supervisor/QC to enhance their Customer Due Diligence (CDD) team. This is an exciting opportunity for an experienced professional to contribute to the protection of the organisation against financial crime and sanctions-related risks. Key Responsibilities Act as the subject matter expert in the first line of defence model, identifying financial crime risks during client onboarding and periodic due diligence processes. Ensure accurate completion of customer information on CDD and operational systems, validating and screening data thoroughly. Conduct quality control (QC) checks and approve the work of analysts, ensuring adherence to the organisation's standards and procedures. Produce documentation and assist in daily workflows, especially during peak business activities. Monitor the Bank's internal sanctions screening tool, ensuring timely reviews and accurate documentation for regulatory compliance. Prepare and check sanctions validation packs, conducting thorough research and analysis of client exposure to sensitive countries. Liaise with various stakeholders across departments, providing expert advice on CDD and documentation matters. Support the ongoing training and development of junior staff, fostering a collaborative team environment. Qualifications and Skills Strong understanding of financial crime, sanctions, and AML regulations. Externally recognised qualifications in AML and customer due diligence (e.g., ICA Certificates, ACAMS) preferred. Excellent communication skills, both written and verbal, with the ability to convey complex information clearly. Proven analytical skills with a keen eye for detail and accuracy in documentation and reporting. Experience in mentoring and coaching team members, providing constructive feedback in a supportive manner. Proficiency in relevant systems (e.g., LJ Jones, Moody's Orbis, FircoSoft) is desirable. Why Join Us? This role presents a unique chance to impact the organisation's financial crime prevention efforts actively. You will collaborate with a diverse team, enhancing your expertise in compliance and regulatory matters. If you are self-sufficient, proactive, and ready to take on new challenges, we encourage you to apply. We use generative AI tools to support our candidate screening process. This helps us ensure a fair, consistent, and efficient experience for all applicants. Rest assured, all final decisions are made by our hiring team, and your application will be reviewed with care and attention. Adecco is a disability-confident employer. It is important to us that we run an inclusive and accessible recruitment process to support candidates of all backgrounds and all abilities to apply. Adecco is committed to building a supportive environment for you to explore the next steps in your career. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you.
Randstad Construction & Property
Nottingham, Nottinghamshire
Randstad are partnering with one of the UK's fastest-growing safety and compliance businesses for this dual role of Asbestos Surveyor Analyst . Our client isn't looking for someone to just blend into the background; they want a trusted professional who genuinely enjoys being out in the field and taking charge of both surveying and analytical duties. If you thrive in a dynamic role where your expertise directly impacts site safety and abatement projects, and you want an employer that rewards your hard work with a completely transparent, stress-free package, this could be the perfect fit. Location: Covering North, East and West Midlands Salary: £33,000 - £40,000 Package: 25 days holiday (increasing 1 day per year of service) Stakeholder Pension, Life cover, Employee Assistance Programme, and a Health policy Total flexibility to choose a standard company car, a commercial van, or opt for a cash allowance What you'll actually be doing day-to-day: You'll travel to various client premises to competently undertake technical asbestos inspections, bulk sampling, and testing. You'll step into a management capacity for abatement schemes, ensuring everything aligns with legislative guidance, LARC, PoW, and internal RAMs. You'll own the process for successfully completing four-stage clearances and site re-occupations, liaising directly with clients, site representatives, and licensed removal operatives. Using modern reporting formats like PDAs, you'll produce highly accurate survey data, factual test reports, method statements, and detailed site plans. You will help train up newer staff, provide proactive feedback to management on site conditions, and offer clear, impartial advice to build strong client relationships. You'll strictly adhere to the UKAS accredited management system, stay on top of your own quality control (QC) and quality assurance (QA) schemes, and take proper care of your allocated vehicle and equipment. What you need to bring to the table: Must hold both your BOHS P402 and your BOHS P403/P404 (or the RSPH equivalents). Maintain valid personal site access accreditation's, like a CSCS card. Additional qualifications like a BOHS P406, W504 (S301), or a Certificate of Competence in Asbestos (CoCA) are advantageous Solid, hands-on experience performing both surveying and analytical duties across a variety of site environments. Have a highly methodical mentality, be IT literate, and comfortable working under your own initiative, and armed with a flexible, problem-solving "can-do" attitude. Why you'll love the setup: Our client genuinely listens to their field staff and has built a package that makes life easier and rewards hard work: No Travel-Time Headaches: Forget meticulously calculating door-to-door hours; your travel time is already baked right into your base salary to keep things simple. Fair Overtime: Enjoy a straightforward, fixed-rate structure for any weekend or night shifts. Your Ride, Your Choice: Total flexibility to choose a standard company car (like a hybrid estate), a commercial van, or opt for a cash allowance. Real Career Progression: Our client has a fantastic culture of promoting from within, meaning you can build a long-term, rewarding career with a management team that truly understands what you do. Interested? Apply today with an up to date CV Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application. Candidates must be eligible to live and work in the UK. For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
Aug 20, 2026
Full time
Randstad are partnering with one of the UK's fastest-growing safety and compliance businesses for this dual role of Asbestos Surveyor Analyst . Our client isn't looking for someone to just blend into the background; they want a trusted professional who genuinely enjoys being out in the field and taking charge of both surveying and analytical duties. If you thrive in a dynamic role where your expertise directly impacts site safety and abatement projects, and you want an employer that rewards your hard work with a completely transparent, stress-free package, this could be the perfect fit. Location: Covering North, East and West Midlands Salary: £33,000 - £40,000 Package: 25 days holiday (increasing 1 day per year of service) Stakeholder Pension, Life cover, Employee Assistance Programme, and a Health policy Total flexibility to choose a standard company car, a commercial van, or opt for a cash allowance What you'll actually be doing day-to-day: You'll travel to various client premises to competently undertake technical asbestos inspections, bulk sampling, and testing. You'll step into a management capacity for abatement schemes, ensuring everything aligns with legislative guidance, LARC, PoW, and internal RAMs. You'll own the process for successfully completing four-stage clearances and site re-occupations, liaising directly with clients, site representatives, and licensed removal operatives. Using modern reporting formats like PDAs, you'll produce highly accurate survey data, factual test reports, method statements, and detailed site plans. You will help train up newer staff, provide proactive feedback to management on site conditions, and offer clear, impartial advice to build strong client relationships. You'll strictly adhere to the UKAS accredited management system, stay on top of your own quality control (QC) and quality assurance (QA) schemes, and take proper care of your allocated vehicle and equipment. What you need to bring to the table: Must hold both your BOHS P402 and your BOHS P403/P404 (or the RSPH equivalents). Maintain valid personal site access accreditation's, like a CSCS card. Additional qualifications like a BOHS P406, W504 (S301), or a Certificate of Competence in Asbestos (CoCA) are advantageous Solid, hands-on experience performing both surveying and analytical duties across a variety of site environments. Have a highly methodical mentality, be IT literate, and comfortable working under your own initiative, and armed with a flexible, problem-solving "can-do" attitude. Why you'll love the setup: Our client genuinely listens to their field staff and has built a package that makes life easier and rewards hard work: No Travel-Time Headaches: Forget meticulously calculating door-to-door hours; your travel time is already baked right into your base salary to keep things simple. Fair Overtime: Enjoy a straightforward, fixed-rate structure for any weekend or night shifts. Your Ride, Your Choice: Total flexibility to choose a standard company car (like a hybrid estate), a commercial van, or opt for a cash allowance. Real Career Progression: Our client has a fantastic culture of promoting from within, meaning you can build a long-term, rewarding career with a management team that truly understands what you do. Interested? Apply today with an up to date CV Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application. Candidates must be eligible to live and work in the UK. For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
About the Role Smart4Sciences is working with a leading healthcare organisation to recruit a QC Stability Lead to join their Quality Control team in Hull. This is an excellent opportunity for an experienced QC Analyst / Pharmaceutical Analyst looking to take on a lead-level position. You will join a team of 8 analysts, providing technical and troubleshooting support across laboratory equipment, analytical methods and systems. Key Responsibilities Provide technical support and troubleshooting guidance to the QC analytical team. Support troubleshooting of laboratory equipment, systems and analytical methods. Carry out pharmaceutical analysis in accordance with GMP requirements. Perform analytical testing using techniques including HPLC, GC and Karl Fischer . Provide technical guidance and support to other analysts within the team. Assist with analytical method troubleshooting where required. Ensure laboratory activities are carried out in accordance with GMP requirements and relevant procedures. Work closely with the Head of QC to support the effective technical operation of the laboratory. About you: Strong experience within pharmaceutical QC/analytical testing. Hands-on experience with HPLC, GC and Karl Fischer. Experience working within a GMP-accredited laboratory environment. Strong analytical troubleshooting and problem-solving skills. Experience troubleshooting laboratory equipment, systems and analytical methods. The confidence to provide technical guidance and support to other analysts. Excellent attention to detail and a methodical approach to laboratory work. Apply Now If you are an experienced pharmaceutical analyst with strong analytical and troubleshooting experience and are looking for the next step in your QC career, we would be keen to hear from you.
Aug 20, 2026
Full time
About the Role Smart4Sciences is working with a leading healthcare organisation to recruit a QC Stability Lead to join their Quality Control team in Hull. This is an excellent opportunity for an experienced QC Analyst / Pharmaceutical Analyst looking to take on a lead-level position. You will join a team of 8 analysts, providing technical and troubleshooting support across laboratory equipment, analytical methods and systems. Key Responsibilities Provide technical support and troubleshooting guidance to the QC analytical team. Support troubleshooting of laboratory equipment, systems and analytical methods. Carry out pharmaceutical analysis in accordance with GMP requirements. Perform analytical testing using techniques including HPLC, GC and Karl Fischer . Provide technical guidance and support to other analysts within the team. Assist with analytical method troubleshooting where required. Ensure laboratory activities are carried out in accordance with GMP requirements and relevant procedures. Work closely with the Head of QC to support the effective technical operation of the laboratory. About you: Strong experience within pharmaceutical QC/analytical testing. Hands-on experience with HPLC, GC and Karl Fischer. Experience working within a GMP-accredited laboratory environment. Strong analytical troubleshooting and problem-solving skills. Experience troubleshooting laboratory equipment, systems and analytical methods. The confidence to provide technical guidance and support to other analysts. Excellent attention to detail and a methodical approach to laboratory work. Apply Now If you are an experienced pharmaceutical analyst with strong analytical and troubleshooting experience and are looking for the next step in your QC career, we would be keen to hear from you.
Do you have experience driving multinational growth by creating unique solutions in the martech and adtech space? If so, this MarTech Analyst opportunity may be the perfect fit for you. The Opportunity: As a Marketing Technology Analyst, you will help with the coordination and daily management of marketing tools and platforms used by the marketing department. Reporting to the Marketing Technology Manager, you will coordinate the efforts between marketing and third-party contractors, consultants and internal IT staff to complete projects according to plan. You will work with management and marketing channels to establish a project's goals and oversee quality control throughout its life cycle. The Day-to-Day: Help with ongoing monitoring and enhancements of platforms/tools in the Marketing technology stack, including cross platform integrations and managing technical vendors Configure advertising and marketing technology platforms to support global marketing measurement and activation across digital marketing experiences Communicate business enhancements and modifications - verbally or through written documentation - to senior management, peers, staff and other employees so that issues and solutions are understood Capture and document requirements for system enhancements from global marketing team Conduct trainings and provide technical expertise and support for global marketing Ensure quality, uptime and accuracy of tech stack Qualifications: 3+ years of professional experience in marketing technology or IT; Bachelor's degree or equivalent combination of education and experience Hands-on experience with web analytics, digital content management and marketing automation tools Ability to write and troubleshoot JavaScript, HTML and CSS Familiarity with web debugging tools, CMS, Analytics, A/B testing tools, TMS, Manual/Automated QC, Ad Tech platforms (Facebook for Business, Google Adwords, Tealium) Familiarity with Excel, macros, and SQL scripting/editing Why Fisher Investments Europe: The global Fisher organisation distinguishes itself by putting clients first, providing unmatched service, and taking a personalised approach to investing. You can feel confident knowing that we align with our clients' best interests by using a simple and transparent fee structure and recognised European custodians. It's the people that make the Fisher purpose possible, and to help our employees meet their long-term goals, we offer an array of benefits, including: 100% paid premiums for our top-tier supplemental medical, dental and annual health screening plans for employees and their qualified dependents 28 days annual leave, with the ability to purchase up to 3 additional days per year, plus up to 8 paid holidays Enhanced maternity pay package with 16 weeks' top up to full base pay for eligible employees $10,000 fertility, hormonal health and family-forming benefit A retirement pension plan, featuring a 9% company contribution of base pay with an additional company match of up to 5% of base pay on personal contributions Gym subsidy of up to £50 per month Employee Assistance Program and other emotional wellbeing services A collaborative working environment that practises ongoing training, educational support and employee appreciation events This is an in-office role. Based on your role, tenure, and performance eligibility you may have the opportunity to participate in our hybrid work from home program. This program is subject to change. Employees residing outside of the US will be eligible for the $10,000 equivalent in their local currency. FISHER INVESTMENTS EUROPE IS AN EQUAL OPPORTUNITY EMPLOYER
Aug 16, 2026
Full time
Do you have experience driving multinational growth by creating unique solutions in the martech and adtech space? If so, this MarTech Analyst opportunity may be the perfect fit for you. The Opportunity: As a Marketing Technology Analyst, you will help with the coordination and daily management of marketing tools and platforms used by the marketing department. Reporting to the Marketing Technology Manager, you will coordinate the efforts between marketing and third-party contractors, consultants and internal IT staff to complete projects according to plan. You will work with management and marketing channels to establish a project's goals and oversee quality control throughout its life cycle. The Day-to-Day: Help with ongoing monitoring and enhancements of platforms/tools in the Marketing technology stack, including cross platform integrations and managing technical vendors Configure advertising and marketing technology platforms to support global marketing measurement and activation across digital marketing experiences Communicate business enhancements and modifications - verbally or through written documentation - to senior management, peers, staff and other employees so that issues and solutions are understood Capture and document requirements for system enhancements from global marketing team Conduct trainings and provide technical expertise and support for global marketing Ensure quality, uptime and accuracy of tech stack Qualifications: 3+ years of professional experience in marketing technology or IT; Bachelor's degree or equivalent combination of education and experience Hands-on experience with web analytics, digital content management and marketing automation tools Ability to write and troubleshoot JavaScript, HTML and CSS Familiarity with web debugging tools, CMS, Analytics, A/B testing tools, TMS, Manual/Automated QC, Ad Tech platforms (Facebook for Business, Google Adwords, Tealium) Familiarity with Excel, macros, and SQL scripting/editing Why Fisher Investments Europe: The global Fisher organisation distinguishes itself by putting clients first, providing unmatched service, and taking a personalised approach to investing. You can feel confident knowing that we align with our clients' best interests by using a simple and transparent fee structure and recognised European custodians. It's the people that make the Fisher purpose possible, and to help our employees meet their long-term goals, we offer an array of benefits, including: 100% paid premiums for our top-tier supplemental medical, dental and annual health screening plans for employees and their qualified dependents 28 days annual leave, with the ability to purchase up to 3 additional days per year, plus up to 8 paid holidays Enhanced maternity pay package with 16 weeks' top up to full base pay for eligible employees $10,000 fertility, hormonal health and family-forming benefit A retirement pension plan, featuring a 9% company contribution of base pay with an additional company match of up to 5% of base pay on personal contributions Gym subsidy of up to £50 per month Employee Assistance Program and other emotional wellbeing services A collaborative working environment that practises ongoing training, educational support and employee appreciation events This is an in-office role. Based on your role, tenure, and performance eligibility you may have the opportunity to participate in our hybrid work from home program. This program is subject to change. Employees residing outside of the US will be eligible for the $10,000 equivalent in their local currency. FISHER INVESTMENTS EUROPE IS AN EQUAL OPPORTUNITY EMPLOYER
Assistant Laboratory AnalystApplylocations: Truro Laboratorytime type: Full timeposted on: Posted Todayjob requisition id: JR102330We are pleased to be offering a great opportunity to work in the leading Mineral Processing Testing Facility in Europe. SLR Consulting are looking to hire an Assistant Laboratory Analyst as part of their Analytical Team. The individual would be involved in assisting the preparation of test work and ore samples for elemental analysis in the Analytical Laboratory. This is a full-time position working primarily between 08:30 - 16:30 subject to work requirements. Please note that the laboratory location (Wheal Jane Earth Science Park, Baldhu, Truro, TR3 6EE) is not easily accessible by public transport and therefore the commute needs to be seriously considered when applying. Typical responsibilities include: • Entering sample data into the laboratory sample tracking system in accordance with standard procedures, • Supporting the analytical chemists with sample preparation, preparation of laboratory reagents and solutions etc as and when required, • Maintaining QA/QC databases, • Complying with standard analytical procedures, • Maintaining, calibrating and cleaning equipment as appropriate, • Working in a methodical manner quickly and efficiently, • Assisting with general tidying of the laboratory, • Monitoring stock levels and ordering chemicals, • Disposing of chemicals and waste products safely, • Working in a safe manner, abiding by company SSOW and COSHH regulations at all times. A successful candidate will require: • Good team working and communication skills, • Ability to manage time to maximise productivity, Ability to quickly and accurately conduct required quality control tests, • Safe and responsible working manner in laboratory areas, • Ability to work unsupervised, • Attention to detail and accuracy of recording information, • Awareness of commercial importance of products and ability to plan and prioritise work accordingly. • Qualified to a minimum of GCSE standard in English and Maths. • Experience of similar work is an advantage but not essential as training will be given. About us We provised high quality metallurgical testwork programmes ranging from initial bench scoping investigations to feasibility studies and pilot plant campaigns. We have extensive experience on a variety of ore and commodity types from across the world. Our metallurgical testing forms a key part of the overall development of a mining project, with testing being conducted to the highest standard and consideration made to the overall project economics, as well as metallurgical performance. SLR are global leaders in Sustainability Solutions, helping our clients achieve their sustainability goals. We are a consultancy with 4000+ employees across 6 regions in over 125 countries. Our 'one team' culture is at the heart of our business, providing a collaborative and supportive environment for professional development. Along with competitive salaries, our staff enjoy a comprehensive benefits package with a company pension plus excellent healthcare offering, travel and life insurance and a structured career framework with regular reviews offering outstanding opportunities for progression. Alongside 25 day's annual leave, with additional flexible bank holidays, we offer flexible, agile and hybrid working which enables staff to tailor hours worked around core hours, with family friendly policies help balance the needs of professional and home life. Culture & Inclusion at SLR We are committed to being an equal opportunities employer, and our expectations go beyond purely complying with legislation. Through our Regional C&I Committees, Global Council and Employee Networks, we foster an inclusive environment where all people regardless of their background can thrive.We welcome applications from all individuals, regardless of their background, including those from groups that are currently under-represented at SLR, such as people identifying as 2SLGBTQI+, Indigenous peoples, ethnic minority groups, women, and people with visible or invisible disabilities, including those who are neurodivergent.Should you require any special adjustments throughout the recruitment process with us, please let us know. As a Disability Confident Committed employer, we seek to ensure all applicants have equitable support when applying to SLR. SLR Commitment - All applicants with a disability who meet the essential requirements for the job will be guaranteed an interview in line with our Disability Confident Committed status.
Jul 31, 2026
Full time
Assistant Laboratory AnalystApplylocations: Truro Laboratorytime type: Full timeposted on: Posted Todayjob requisition id: JR102330We are pleased to be offering a great opportunity to work in the leading Mineral Processing Testing Facility in Europe. SLR Consulting are looking to hire an Assistant Laboratory Analyst as part of their Analytical Team. The individual would be involved in assisting the preparation of test work and ore samples for elemental analysis in the Analytical Laboratory. This is a full-time position working primarily between 08:30 - 16:30 subject to work requirements. Please note that the laboratory location (Wheal Jane Earth Science Park, Baldhu, Truro, TR3 6EE) is not easily accessible by public transport and therefore the commute needs to be seriously considered when applying. Typical responsibilities include: • Entering sample data into the laboratory sample tracking system in accordance with standard procedures, • Supporting the analytical chemists with sample preparation, preparation of laboratory reagents and solutions etc as and when required, • Maintaining QA/QC databases, • Complying with standard analytical procedures, • Maintaining, calibrating and cleaning equipment as appropriate, • Working in a methodical manner quickly and efficiently, • Assisting with general tidying of the laboratory, • Monitoring stock levels and ordering chemicals, • Disposing of chemicals and waste products safely, • Working in a safe manner, abiding by company SSOW and COSHH regulations at all times. A successful candidate will require: • Good team working and communication skills, • Ability to manage time to maximise productivity, Ability to quickly and accurately conduct required quality control tests, • Safe and responsible working manner in laboratory areas, • Ability to work unsupervised, • Attention to detail and accuracy of recording information, • Awareness of commercial importance of products and ability to plan and prioritise work accordingly. • Qualified to a minimum of GCSE standard in English and Maths. • Experience of similar work is an advantage but not essential as training will be given. About us We provised high quality metallurgical testwork programmes ranging from initial bench scoping investigations to feasibility studies and pilot plant campaigns. We have extensive experience on a variety of ore and commodity types from across the world. Our metallurgical testing forms a key part of the overall development of a mining project, with testing being conducted to the highest standard and consideration made to the overall project economics, as well as metallurgical performance. SLR are global leaders in Sustainability Solutions, helping our clients achieve their sustainability goals. We are a consultancy with 4000+ employees across 6 regions in over 125 countries. Our 'one team' culture is at the heart of our business, providing a collaborative and supportive environment for professional development. Along with competitive salaries, our staff enjoy a comprehensive benefits package with a company pension plus excellent healthcare offering, travel and life insurance and a structured career framework with regular reviews offering outstanding opportunities for progression. Alongside 25 day's annual leave, with additional flexible bank holidays, we offer flexible, agile and hybrid working which enables staff to tailor hours worked around core hours, with family friendly policies help balance the needs of professional and home life. Culture & Inclusion at SLR We are committed to being an equal opportunities employer, and our expectations go beyond purely complying with legislation. Through our Regional C&I Committees, Global Council and Employee Networks, we foster an inclusive environment where all people regardless of their background can thrive.We welcome applications from all individuals, regardless of their background, including those from groups that are currently under-represented at SLR, such as people identifying as 2SLGBTQI+, Indigenous peoples, ethnic minority groups, women, and people with visible or invisible disabilities, including those who are neurodivergent.Should you require any special adjustments throughout the recruitment process with us, please let us know. As a Disability Confident Committed employer, we seek to ensure all applicants have equitable support when applying to SLR. SLR Commitment - All applicants with a disability who meet the essential requirements for the job will be guaranteed an interview in line with our Disability Confident Committed status.
Data Quality Control AnalystSkip to main contentFifty5Blue are committed to protecting and respecting your privacy. As a global business, we are committed to your privacy, and our obligations under the data protection laws which apply in your region. For further details, you may access a complete copy of Fifty5Blue employee data privacy policy here: Privacy and Cookies Policy - Fifty5Blue# Fifty5BlueData Quality Control Analyst page is loaded Data Quality Control AnalystApplylocations: London, Westgatetime type: Full timeposted on: Posted Yesterdaytime left to apply: End Date: August 31, 2026 (30+ days left to apply)job requisition id: R100240We help partners understand the changing advertising landscape. Specialising in audience measurement, consumer targeting and in-depth intelligence into paid, owned and earned media, their global coverage and local expertise enable better understanding of media audiences and their relationships with brands. Job Details Job Title: Quality Control Analyst Location: London, Hanger Lane Full-time/Permanent/Hybrid Job Details BARB (The Broadcasters' Audience Research Board) is responsible for the measurement of the number of people watching television in the UK, on behalf of the television companies and the advertising industry.The BARB Operations team is responsible for delivering daily TV ratings to the UKs broadcast industry and associated agencies. This is the UK's currency measurement, and the service is contracted out by BARB (Broadcasters Audience Research Board) to research companies that perform this function for them. There are currently 8000 homes on the BARB panel from which viewing data is collected daily. In addition to the information collected about viewing of broadcast content on the TV set, a separate piece of equipment called a Focal Meter is used to capture online viewing from each of our broadband homes. Tasks & Responsibilities This role is for a QC Analyst within a team of 7. Evaluating the data received from BARB homes and deciding on whether any potential faults need to be followed up. Reviewing data collected from new homes and deciding on whether a home has passed all the vital checks and criteria to become a live home on the active panel. Collaborating closely with the internal Panel Admin Team and external field engineers to progress issues precluding homes from reporting accurately. Helping to provide information and guidance to field engineers on the source of problems causing issues with data quality. Using a wide of tools and dashboards to investigate issues that might have a detrimental impact on data quality. Perform investigations to understand any unusual trends or patterns of viewing behaviour observed in daily results. Supervise the performance and efficiency of other members of the BARB team, including technicians and data entry Ensuring that all procedures are carried out in accordance with the client specification Undertake QC activities within specified timeframes to ensure that contracts' Service Level Agreements are satisfied Your Profile and Key Skills We Are Looking For Good knowledge and experience in Microsoft Office tools, especially Excel, Access and Power BI. Experience of running statistical data analyses in a previous role or to satisfy an academic qualification. Familiarity with various tools and dashboards used for data investigation and quality control. Preferred but not essential (SQL/Python) Ability to evaluate and interpret data accurately to identify potential faults and unusual trends. Good time management skills. A confident person with good communication skills Would need to be prepared to work unsociable hours on a rota basis at weekends and bank holidays. Country United Kingdom Why join Fifty5Blue? We pride ourselves on understanding people, and what makes us think and act the way we do. And because we know people, we like to make sure our own people are being looked after as well. Equality of opportunity for everyone is our highest priority and we support our colleagues to work in a way that supports their health and wellbeing. While we encourage teams to spend part of their working week in the office, we understand no one size fits all; our approach is flexible to ensure everybody feels included, accepted, and that we can win together. We're dedicated to creating an inclusive culture and value the diversity of our people, clients, suppliers and communities, and we encourage applications from all backgrounds and sections of society. Even if you feel like you're not an exact match, we'd love to receive your application and talk to you about this job or others at Fifty5Blue. About UsFifty5Blue is a global leader in media measurement and analytics, operating in more than 80 countries.We bring clarity to complexity. Our independent, hybrid cross-media audience measurement combines trusted audience panels with large-scale data to establish a single, coherent view across platforms and markets. This gives content owners, advertisers, agencies and platforms the clarity and confidence to develop content and plan advertising decisively.With deep expertise across global media systems, we design integrated, comparable measurement frameworks that support a more consistent and accountable media market. Why join Fifty5Blue?Our specialist expertise, pioneering technology and commitment to innovation provide the ideal environment for career growth.Want to have a real-world impact? Help us deliver the trusted data that informs decisions in content and advertising across the world.When you join us, you'll gain the benefit of our global reach, advanced technical innovation and deep expertise. We'll support you with training and career development opportunities. Become part of a community of passionate, dedicated professionals.
Jul 31, 2026
Full time
Data Quality Control AnalystSkip to main contentFifty5Blue are committed to protecting and respecting your privacy. As a global business, we are committed to your privacy, and our obligations under the data protection laws which apply in your region. For further details, you may access a complete copy of Fifty5Blue employee data privacy policy here: Privacy and Cookies Policy - Fifty5Blue# Fifty5BlueData Quality Control Analyst page is loaded Data Quality Control AnalystApplylocations: London, Westgatetime type: Full timeposted on: Posted Yesterdaytime left to apply: End Date: August 31, 2026 (30+ days left to apply)job requisition id: R100240We help partners understand the changing advertising landscape. Specialising in audience measurement, consumer targeting and in-depth intelligence into paid, owned and earned media, their global coverage and local expertise enable better understanding of media audiences and their relationships with brands. Job Details Job Title: Quality Control Analyst Location: London, Hanger Lane Full-time/Permanent/Hybrid Job Details BARB (The Broadcasters' Audience Research Board) is responsible for the measurement of the number of people watching television in the UK, on behalf of the television companies and the advertising industry.The BARB Operations team is responsible for delivering daily TV ratings to the UKs broadcast industry and associated agencies. This is the UK's currency measurement, and the service is contracted out by BARB (Broadcasters Audience Research Board) to research companies that perform this function for them. There are currently 8000 homes on the BARB panel from which viewing data is collected daily. In addition to the information collected about viewing of broadcast content on the TV set, a separate piece of equipment called a Focal Meter is used to capture online viewing from each of our broadband homes. Tasks & Responsibilities This role is for a QC Analyst within a team of 7. Evaluating the data received from BARB homes and deciding on whether any potential faults need to be followed up. Reviewing data collected from new homes and deciding on whether a home has passed all the vital checks and criteria to become a live home on the active panel. Collaborating closely with the internal Panel Admin Team and external field engineers to progress issues precluding homes from reporting accurately. Helping to provide information and guidance to field engineers on the source of problems causing issues with data quality. Using a wide of tools and dashboards to investigate issues that might have a detrimental impact on data quality. Perform investigations to understand any unusual trends or patterns of viewing behaviour observed in daily results. Supervise the performance and efficiency of other members of the BARB team, including technicians and data entry Ensuring that all procedures are carried out in accordance with the client specification Undertake QC activities within specified timeframes to ensure that contracts' Service Level Agreements are satisfied Your Profile and Key Skills We Are Looking For Good knowledge and experience in Microsoft Office tools, especially Excel, Access and Power BI. Experience of running statistical data analyses in a previous role or to satisfy an academic qualification. Familiarity with various tools and dashboards used for data investigation and quality control. Preferred but not essential (SQL/Python) Ability to evaluate and interpret data accurately to identify potential faults and unusual trends. Good time management skills. A confident person with good communication skills Would need to be prepared to work unsociable hours on a rota basis at weekends and bank holidays. Country United Kingdom Why join Fifty5Blue? We pride ourselves on understanding people, and what makes us think and act the way we do. And because we know people, we like to make sure our own people are being looked after as well. Equality of opportunity for everyone is our highest priority and we support our colleagues to work in a way that supports their health and wellbeing. While we encourage teams to spend part of their working week in the office, we understand no one size fits all; our approach is flexible to ensure everybody feels included, accepted, and that we can win together. We're dedicated to creating an inclusive culture and value the diversity of our people, clients, suppliers and communities, and we encourage applications from all backgrounds and sections of society. Even if you feel like you're not an exact match, we'd love to receive your application and talk to you about this job or others at Fifty5Blue. About UsFifty5Blue is a global leader in media measurement and analytics, operating in more than 80 countries.We bring clarity to complexity. Our independent, hybrid cross-media audience measurement combines trusted audience panels with large-scale data to establish a single, coherent view across platforms and markets. This gives content owners, advertisers, agencies and platforms the clarity and confidence to develop content and plan advertising decisively.With deep expertise across global media systems, we design integrated, comparable measurement frameworks that support a more consistent and accountable media market. Why join Fifty5Blue?Our specialist expertise, pioneering technology and commitment to innovation provide the ideal environment for career growth.Want to have a real-world impact? Help us deliver the trusted data that informs decisions in content and advertising across the world.When you join us, you'll gain the benefit of our global reach, advanced technical innovation and deep expertise. We'll support you with training and career development opportunities. Become part of a community of passionate, dedicated professionals.
QC Team Leader Dundee 45,000 - 50,000 + 5% Bonus + Excellent Benefits Are you an experienced Quality Control professional looking to take the next step in your leadership career? We're recruiting for a QC Team Leader to join a well-established pharmaceutical manufacturing business during an exciting period of investment and growth. This is an opportunity to lead a team of QC Analysts, play a key role in developing laboratory capability and help drive quality, compliance and continuous improvement across the site. This is a hands-on leadership role where you'll combine your technical laboratory knowledge with people management responsibilities, supporting the day-to-day operation of the QC laboratory whilst ensuring the highest standards of GMP and regulatory compliance. Key Responsibilities Lead, coach and develop a team of QC Analysts. Oversee day-to-day laboratory activities and workload planning. Review QC testing across raw materials, in-process, finished products and stability samples. Support investigations, CAPAs, change controls and continuous improvement activities. Ensure compliance with GMP, GLP and Data Integrity requirements. Review and update SOPs, analytical methods and laboratory documentation. Work closely with QA, Manufacturing and other departments to support operational priorities. Promote a positive quality culture and support ongoing team development. About You We're keen to speak with candidates who have: Experience leading or supervising a Quality Control laboratory team. A pharmaceutical manufacturing background. Strong knowledge of GMP and pharmaceutical quality standards. Experience of chromatography techniques such as HPLC and/or GC. Experience supporting investigations, CAPAs and quality systems. The ability to coach, develop and motivate others. A degree in a scientific discipline or equivalent industry experience. Package 45,000 - 50,000 basic salary 5% annual bonus Private medical insurance Medicash scheme 30 days' annual leave (inclusive of public holidays) 5% employer pension contribution Excellent long-term career development If you're looking for a leadership opportunity within a growing pharmaceutical manufacturing environment, we'd love to hear from you.
Jul 31, 2026
Full time
QC Team Leader Dundee 45,000 - 50,000 + 5% Bonus + Excellent Benefits Are you an experienced Quality Control professional looking to take the next step in your leadership career? We're recruiting for a QC Team Leader to join a well-established pharmaceutical manufacturing business during an exciting period of investment and growth. This is an opportunity to lead a team of QC Analysts, play a key role in developing laboratory capability and help drive quality, compliance and continuous improvement across the site. This is a hands-on leadership role where you'll combine your technical laboratory knowledge with people management responsibilities, supporting the day-to-day operation of the QC laboratory whilst ensuring the highest standards of GMP and regulatory compliance. Key Responsibilities Lead, coach and develop a team of QC Analysts. Oversee day-to-day laboratory activities and workload planning. Review QC testing across raw materials, in-process, finished products and stability samples. Support investigations, CAPAs, change controls and continuous improvement activities. Ensure compliance with GMP, GLP and Data Integrity requirements. Review and update SOPs, analytical methods and laboratory documentation. Work closely with QA, Manufacturing and other departments to support operational priorities. Promote a positive quality culture and support ongoing team development. About You We're keen to speak with candidates who have: Experience leading or supervising a Quality Control laboratory team. A pharmaceutical manufacturing background. Strong knowledge of GMP and pharmaceutical quality standards. Experience of chromatography techniques such as HPLC and/or GC. Experience supporting investigations, CAPAs and quality systems. The ability to coach, develop and motivate others. A degree in a scientific discipline or equivalent industry experience. Package 45,000 - 50,000 basic salary 5% annual bonus Private medical insurance Medicash scheme 30 days' annual leave (inclusive of public holidays) 5% employer pension contribution Excellent long-term career development If you're looking for a leadership opportunity within a growing pharmaceutical manufacturing environment, we'd love to hear from you.
Rosemont seeks a Senior Analyst - Quality Control (Microbiology) to join our Leeds facility. The role requires leading OOS investigations, CAPA activities and environmental monitoring within a GMP QC lab environment. You will review validation and transfer activities, support regulatory inspections and drive continuous improvement while collaborating with Production, R&D and Project Management teams.
Jul 31, 2026
Full time
Rosemont seeks a Senior Analyst - Quality Control (Microbiology) to join our Leeds facility. The role requires leading OOS investigations, CAPA activities and environmental monitoring within a GMP QC lab environment. You will review validation and transfer activities, support regulatory inspections and drive continuous improvement while collaborating with Production, R&D and Project Management teams.
Senior Analyst - Quality Control (Microbiology) This role requires the successful candidate to be based at our Leeds facility Monday - Friday each week. Key Responsibilities Lead and support Out of Specification (OOS) investigations and root cause analysis activities. Perform QC compliance gap assessments against relevant pharmacopoeial and regulatory requirements. Support method optimisation, verification, validation and transfer activities. Review validation, stability and risk assessment reports. Prepare and review technical transfer protocols and reports. Participate in CAPA implementation, change controls and continuous improvement programmes. Support audit readiness activities and contribute during regulatory and customer audits. Represent Quality Control with key internal stakeholders including Production, R&D and Project Management teams. Contribute to New Product Development (NPD) projects and QC deliverables. Provide coaching, training and technical support to colleagues while deputising for Team Leaders when required. Maintain compliance with GMP, Quality Management Systems and company procedures. About You Degree in Microbiology or equivalent relevant experience. Strong Microbiology Skills and experience in performing Microbiology laboratory work such as Preservative efficacy testing, total viable counts, environmental monitoring and water testing Significant experience working within a GMP laboratory environment. Strong understanding of analytical testing, method validation and laboratory compliance requirements. Experience leading investigations, CAPAs and continuous improvement initiatives. Excellent report writing, problem-solving and risk assessment skills. Ability to work independently whilst managing complex technical issues. Strong communication and stakeholder management capabilities. Strong Team work and organisation skills. Experience in scheduling and planning team activities. 4+ years' experience in a Quality Control analytical laboratory environment. Experience supporting regulatory inspections and customer audits. Leadership, coaching or mentoring experience. Experience supporting pharmaceutical product development or technical transfer activities. At Rosemont, we believe great benefits go beyond salary. That's why our offering is shaped by what our people truly value: Healthcare Cash Plan - Personal cover to support your health and wellbeing 3% Employee / 5% Company Pension Contribution - Helping you plan for the future 26 Days Annual Leave + Bank Holidays Flexible Working - Including hybrid and flexible working hours available. Free On-Site Parking - Convenient access to our Leeds facility Rosemont Rewards Platform - Discounts, free perks, and wellbeing tools for all employees We are committed to fostering an environment of enablement where our people can grow, develop their talents, and pursue meaningful career paths. By placing patients and customers at the heart of everything we do, we drive high performance through accountability, consistency, and a strong governance structure. We champion inclusion, community, and a rewarding employee experience - creating a culture that supports development, celebrates achievement, and empowers individuals to thrive. Diversity & Inclusion is integral to our culture and reflecting the patients we serve. At Rosemont, we believe equal opportunity for all is fundamental to our company's values and all our applicants can expect fairness and transparency in our recruitment process.
Jul 31, 2026
Full time
Senior Analyst - Quality Control (Microbiology) This role requires the successful candidate to be based at our Leeds facility Monday - Friday each week. Key Responsibilities Lead and support Out of Specification (OOS) investigations and root cause analysis activities. Perform QC compliance gap assessments against relevant pharmacopoeial and regulatory requirements. Support method optimisation, verification, validation and transfer activities. Review validation, stability and risk assessment reports. Prepare and review technical transfer protocols and reports. Participate in CAPA implementation, change controls and continuous improvement programmes. Support audit readiness activities and contribute during regulatory and customer audits. Represent Quality Control with key internal stakeholders including Production, R&D and Project Management teams. Contribute to New Product Development (NPD) projects and QC deliverables. Provide coaching, training and technical support to colleagues while deputising for Team Leaders when required. Maintain compliance with GMP, Quality Management Systems and company procedures. About You Degree in Microbiology or equivalent relevant experience. Strong Microbiology Skills and experience in performing Microbiology laboratory work such as Preservative efficacy testing, total viable counts, environmental monitoring and water testing Significant experience working within a GMP laboratory environment. Strong understanding of analytical testing, method validation and laboratory compliance requirements. Experience leading investigations, CAPAs and continuous improvement initiatives. Excellent report writing, problem-solving and risk assessment skills. Ability to work independently whilst managing complex technical issues. Strong communication and stakeholder management capabilities. Strong Team work and organisation skills. Experience in scheduling and planning team activities. 4+ years' experience in a Quality Control analytical laboratory environment. Experience supporting regulatory inspections and customer audits. Leadership, coaching or mentoring experience. Experience supporting pharmaceutical product development or technical transfer activities. At Rosemont, we believe great benefits go beyond salary. That's why our offering is shaped by what our people truly value: Healthcare Cash Plan - Personal cover to support your health and wellbeing 3% Employee / 5% Company Pension Contribution - Helping you plan for the future 26 Days Annual Leave + Bank Holidays Flexible Working - Including hybrid and flexible working hours available. Free On-Site Parking - Convenient access to our Leeds facility Rosemont Rewards Platform - Discounts, free perks, and wellbeing tools for all employees We are committed to fostering an environment of enablement where our people can grow, develop their talents, and pursue meaningful career paths. By placing patients and customers at the heart of everything we do, we drive high performance through accountability, consistency, and a strong governance structure. We champion inclusion, community, and a rewarding employee experience - creating a culture that supports development, celebrates achievement, and empowers individuals to thrive. Diversity & Inclusion is integral to our culture and reflecting the patients we serve. At Rosemont, we believe equal opportunity for all is fundamental to our company's values and all our applicants can expect fairness and transparency in our recruitment process.
Talentmark are recruiting for a QC Microbiology Analyst to join a Pharmaceutical Services Company in Central Belt Scotland. This is a permanent role with Mon-Fri day time working hours and is site based. The Role: You will undertake the tasks and analytical processes involved in method feasibility/development/validation, day to day analysis, data interpretation and documentation of samples for microbiology analysis. Responsibilities: Undertake microbiology analysis and quantitative interpretation of any resultant data generated following defined protocols and procedures. Generate analytical reports and certificates of analysis for any data generated. Complete all assigned work to the appropriate level of science, quality and regulatory compliance. Present a professional manner at all times when dealing with internal and external customers. Carry out all work to the requested specifications and timescales. Ensure all work undertaken meets with the prescribed requirements of the Quality System and the requirements of cGMP. Your Background: Educated to degree level in Microbiology or a related field. Strong Microbiology laboratory skills with the ability to work independently and as part of a team. Experience of Aseptic Technique and experience in a pharmaceutical industry laboratory Experience of working to cGMP. Knowledge of QPulse QMS would be beneficial. Excellent attention to detail, communication and documentation skills. Apply: It is essential all applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence.
Jul 31, 2026
Full time
Talentmark are recruiting for a QC Microbiology Analyst to join a Pharmaceutical Services Company in Central Belt Scotland. This is a permanent role with Mon-Fri day time working hours and is site based. The Role: You will undertake the tasks and analytical processes involved in method feasibility/development/validation, day to day analysis, data interpretation and documentation of samples for microbiology analysis. Responsibilities: Undertake microbiology analysis and quantitative interpretation of any resultant data generated following defined protocols and procedures. Generate analytical reports and certificates of analysis for any data generated. Complete all assigned work to the appropriate level of science, quality and regulatory compliance. Present a professional manner at all times when dealing with internal and external customers. Carry out all work to the requested specifications and timescales. Ensure all work undertaken meets with the prescribed requirements of the Quality System and the requirements of cGMP. Your Background: Educated to degree level in Microbiology or a related field. Strong Microbiology laboratory skills with the ability to work independently and as part of a team. Experience of Aseptic Technique and experience in a pharmaceutical industry laboratory Experience of working to cGMP. Knowledge of QPulse QMS would be beneficial. Excellent attention to detail, communication and documentation skills. Apply: It is essential all applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence.
Randstad are partnering with one of the UK's fastest-growing safety and compliance businesses to find a dedicated Asbestos Analyst. Our client isn't looking for someone to just blend into the background. They want a trusted professional who genuinely enjoys being out in the field and taking charge to ensure site safety. If you thrive in a dynamic role where your analytical expertise directly impacts abatement projects, and you want an employer that rewards your hard work with a completely transparent, stress-free package, this could be the perfect fit. Location: Midlands Salary: 33,000 - 38,000 Package: 25 days holiday (plus 1 day per year of service) Stakeholder pension, Life cover, an Employee Assistance Programme, and Health policy What you'll actually be doing day-to-day: You'll travel to various client premises to competently undertake technical asbestos inspections and testing. You'll manage abatement schemes, ensuring everything aligns with legislative guidance, LARC, PoW, and internal RAMs. You'll liaise directly with clients and licensed removal operatives to successfully complete four-stage clearances and site re-occupations. You'll produce highly accurate, factual test reports, method statements, and site plans. You will help train up newer staff, provide proactive feedback to management on site conditions, and offer clear, impartial advice to build strong client relationships. You'll stay on top of your own quality control (QC) and quality assurance (QA) schemes and take proper care of your allocated vehicle and equipment. What you need to bring to the table: Must hold a BOHS P403/P404 (or the RSPH equivalent) and have valid site access accreditations, like a CSCS card. Highly desirable: BOHS P406, S301, or a Certificate of Competence in Asbestos (CoCA) A background of solid, hands-on experience performing analytical duties across different site environments. Highly methodical mentality, comfortable working under your own initiative, and armed with a flexible, problem-solving "can-do" attitude. The highs of the role: No Travel-Time Headaches: Forget meticulously calculating door-to-door hours; your travel time is already baked right into your base salary to keep things simple. Fair Overtime: Enjoy a straightforward, fixed-rate structure for any weekend or night shifts. Your Ride, Your Choice: Total flexibility to choose a standard company car (like a hybrid estate), a commercial van, or opt for a cash allowance. Real Career Progression: Our client has a fantastic culture of promoting from within, meaning you can build a long-term, rewarding career with a management team that truly understands what you do. Ready to take the next confident step in your analytical career? Apply through Randstad today and let's have a chat! Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application. Candidates must be eligible to live and work in the UK. For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
Jul 30, 2026
Full time
Randstad are partnering with one of the UK's fastest-growing safety and compliance businesses to find a dedicated Asbestos Analyst. Our client isn't looking for someone to just blend into the background. They want a trusted professional who genuinely enjoys being out in the field and taking charge to ensure site safety. If you thrive in a dynamic role where your analytical expertise directly impacts abatement projects, and you want an employer that rewards your hard work with a completely transparent, stress-free package, this could be the perfect fit. Location: Midlands Salary: 33,000 - 38,000 Package: 25 days holiday (plus 1 day per year of service) Stakeholder pension, Life cover, an Employee Assistance Programme, and Health policy What you'll actually be doing day-to-day: You'll travel to various client premises to competently undertake technical asbestos inspections and testing. You'll manage abatement schemes, ensuring everything aligns with legislative guidance, LARC, PoW, and internal RAMs. You'll liaise directly with clients and licensed removal operatives to successfully complete four-stage clearances and site re-occupations. You'll produce highly accurate, factual test reports, method statements, and site plans. You will help train up newer staff, provide proactive feedback to management on site conditions, and offer clear, impartial advice to build strong client relationships. You'll stay on top of your own quality control (QC) and quality assurance (QA) schemes and take proper care of your allocated vehicle and equipment. What you need to bring to the table: Must hold a BOHS P403/P404 (or the RSPH equivalent) and have valid site access accreditations, like a CSCS card. Highly desirable: BOHS P406, S301, or a Certificate of Competence in Asbestos (CoCA) A background of solid, hands-on experience performing analytical duties across different site environments. Highly methodical mentality, comfortable working under your own initiative, and armed with a flexible, problem-solving "can-do" attitude. The highs of the role: No Travel-Time Headaches: Forget meticulously calculating door-to-door hours; your travel time is already baked right into your base salary to keep things simple. Fair Overtime: Enjoy a straightforward, fixed-rate structure for any weekend or night shifts. Your Ride, Your Choice: Total flexibility to choose a standard company car (like a hybrid estate), a commercial van, or opt for a cash allowance. Real Career Progression: Our client has a fantastic culture of promoting from within, meaning you can build a long-term, rewarding career with a management team that truly understands what you do. Ready to take the next confident step in your analytical career? Apply through Randstad today and let's have a chat! Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application. Candidates must be eligible to live and work in the UK. For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
Randstad Construction & Property
Stoke-on-trent, Staffordshire
Randstad are partnering with one of the UK's fastest-growing safety and compliance businesses established just over 20 years ago to find an experienced Asbestos Laboratory Analyst . Our client isn't just looking for someone to go through the motions in the lab. They want a diligent, detail-oriented professional who takes real pride in the accuracy of their work. If you thrive in a process-driven environment where your analysis directly impacts site safety, and you want to work for an employer that genuinely values your expertise with a straightforward, supportive package, this could be the perfect fit. Location: Stoke Salary: 27,000 - 29,000 Package: 25 days holiday, increasing by 1 day every year Stakeholder Pension, Life cover, Employee Assistance Programme, and a Health policy Total flexibility to choose a standard company car, a commercial van, or opt for a cash allowance What you'll actually be doing day-to-day: You'll be responsible for receiving and thoroughly analysing bulk material samples submitted by field staff and third parties for asbestos content. You'll manage your own workload and help your colleagues hit sample KPIs, comfortably aiming for a satisfactory completion of around 70 points each day. You will accurately record your test observations and data to produce highly factual, reliable test reports in both hardcopy and electronic formats. You'll stay on top of your quality control (QC) and quality assurance (QA) schemes, playing a vital role in maintaining the lab's UKAS accreditation and your own authorisation status. You won't just be stuck behind a microscope all day; you'll attend technical meetings, communicate with internal stakeholders, supervise trainees, and occasionally liaise with client representatives to provide factual, impartial advice. Owning your workspace: You will ensure all lab equipment is properly used, well-maintained, and continuously compliant with its calibration status. What you need to bring to the table: Must hold a BOHS P401 (or the RSPH equivalent). Beyond the essential qualification, you need to have proven experience working within the asbestos and/or analytical industries. A person with a highly methodical attitude, process-orientated, and who boasts fantastic attention to detail. Comfortably work under your own initiative while remaining flexible and reliable for the wider team. Ready for a genuine step up in your analytical career? Apply through Randstad today and let's have a chat! Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application. Candidates must be eligible to live and work in the UK. For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
Jul 30, 2026
Full time
Randstad are partnering with one of the UK's fastest-growing safety and compliance businesses established just over 20 years ago to find an experienced Asbestos Laboratory Analyst . Our client isn't just looking for someone to go through the motions in the lab. They want a diligent, detail-oriented professional who takes real pride in the accuracy of their work. If you thrive in a process-driven environment where your analysis directly impacts site safety, and you want to work for an employer that genuinely values your expertise with a straightforward, supportive package, this could be the perfect fit. Location: Stoke Salary: 27,000 - 29,000 Package: 25 days holiday, increasing by 1 day every year Stakeholder Pension, Life cover, Employee Assistance Programme, and a Health policy Total flexibility to choose a standard company car, a commercial van, or opt for a cash allowance What you'll actually be doing day-to-day: You'll be responsible for receiving and thoroughly analysing bulk material samples submitted by field staff and third parties for asbestos content. You'll manage your own workload and help your colleagues hit sample KPIs, comfortably aiming for a satisfactory completion of around 70 points each day. You will accurately record your test observations and data to produce highly factual, reliable test reports in both hardcopy and electronic formats. You'll stay on top of your quality control (QC) and quality assurance (QA) schemes, playing a vital role in maintaining the lab's UKAS accreditation and your own authorisation status. You won't just be stuck behind a microscope all day; you'll attend technical meetings, communicate with internal stakeholders, supervise trainees, and occasionally liaise with client representatives to provide factual, impartial advice. Owning your workspace: You will ensure all lab equipment is properly used, well-maintained, and continuously compliant with its calibration status. What you need to bring to the table: Must hold a BOHS P401 (or the RSPH equivalent). Beyond the essential qualification, you need to have proven experience working within the asbestos and/or analytical industries. A person with a highly methodical attitude, process-orientated, and who boasts fantastic attention to detail. Comfortably work under your own initiative while remaining flexible and reliable for the wider team. Ready for a genuine step up in your analytical career? Apply through Randstad today and let's have a chat! Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application. Candidates must be eligible to live and work in the UK. For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
OGT is a leading global provider of clinical and diagnostic genomic solutions. We believe in creating products and partnerships that enable clinicians to deliver personalised healthcare to patients and that empower clinical researchers to develop the next generation of precision medicines. An opportunity has arisen in our Medical Affairs team for a Medical Affairs QC Analyst. This role offers a varied mix of hands on laboratory work and quality-focused administrative responsibilities, supporting key FISH and NGS processing activities. What you'll be doing for us: Responsible for an assigned proportion of FISH and NGS product testing Act as a subject expert in microscopy and NGS process for the purposes of product testing Adhering to documented procedures for all aspects of laboratory work, ensuring that all relevant information is recorded, products and samples are handled correctly, and that all necessary records and quality data are maintained. Responsible for an appropriate proportion of the quality management system, including procedures and audits. Oversee the smooth and efficient functioning of the laboratory, together with the other MA team members, including consumables, reagents, microscopes, equipment, and software. Contribute to the documentation and infrastructure of the department by providing input into internal protocols and implementation of CAPAs and improvements. Assist with investigations of product, process and equipment nonconformities, validations and process -efficiency initiatives. To comply with all site quality management systems, regulations and health and safety procedures (ISO 9001:2015, ISO 13485:2016, ISO 27001:2022, (EU) 2017/746 (IVDR), GCLP and Human Tissue Act (2004 To complete any other tasks as commensurate with the level and nature of the post as delegated by the line manager. What we are looking for in you: A bachelor's degree in molecular biology, biochemistry, genetics, biotechnology, or similar subject is required, with a minimum of one-year laboratory experience Experience of working in a GLP/GMP environment Basic knowledge of FISH Basic Knowledge of NGS High accuracy and attention to detail Familiarity with working to defined protocols or standard operating procedures (SOPs) Able to work accurately and efficiently in a high-volume, process-driven, and protocol-driven environment Strong team work ethic and commitment to successfully deliver to tight deadlines are essential. Previous experience with FISH analysis is highly advantageous Experience in microscopy is advantageous Proficiency in molecular biology techniques is highly advantageous Experience in NGS based analysis is advantageous. In return you will receive: Private Health Insurance Group Income Protection Group Life Assurance High Street Discount Scheme. Application is via CV and a one-page covering letter outlining your suitability for the role, salary expectations and notice period. Please note that we will need to establish your right to work during the recruitment process.
May 30, 2026
Full time
OGT is a leading global provider of clinical and diagnostic genomic solutions. We believe in creating products and partnerships that enable clinicians to deliver personalised healthcare to patients and that empower clinical researchers to develop the next generation of precision medicines. An opportunity has arisen in our Medical Affairs team for a Medical Affairs QC Analyst. This role offers a varied mix of hands on laboratory work and quality-focused administrative responsibilities, supporting key FISH and NGS processing activities. What you'll be doing for us: Responsible for an assigned proportion of FISH and NGS product testing Act as a subject expert in microscopy and NGS process for the purposes of product testing Adhering to documented procedures for all aspects of laboratory work, ensuring that all relevant information is recorded, products and samples are handled correctly, and that all necessary records and quality data are maintained. Responsible for an appropriate proportion of the quality management system, including procedures and audits. Oversee the smooth and efficient functioning of the laboratory, together with the other MA team members, including consumables, reagents, microscopes, equipment, and software. Contribute to the documentation and infrastructure of the department by providing input into internal protocols and implementation of CAPAs and improvements. Assist with investigations of product, process and equipment nonconformities, validations and process -efficiency initiatives. To comply with all site quality management systems, regulations and health and safety procedures (ISO 9001:2015, ISO 13485:2016, ISO 27001:2022, (EU) 2017/746 (IVDR), GCLP and Human Tissue Act (2004 To complete any other tasks as commensurate with the level and nature of the post as delegated by the line manager. What we are looking for in you: A bachelor's degree in molecular biology, biochemistry, genetics, biotechnology, or similar subject is required, with a minimum of one-year laboratory experience Experience of working in a GLP/GMP environment Basic knowledge of FISH Basic Knowledge of NGS High accuracy and attention to detail Familiarity with working to defined protocols or standard operating procedures (SOPs) Able to work accurately and efficiently in a high-volume, process-driven, and protocol-driven environment Strong team work ethic and commitment to successfully deliver to tight deadlines are essential. Previous experience with FISH analysis is highly advantageous Experience in microscopy is advantageous Proficiency in molecular biology techniques is highly advantageous Experience in NGS based analysis is advantageous. In return you will receive: Private Health Insurance Group Income Protection Group Life Assurance High Street Discount Scheme. Application is via CV and a one-page covering letter outlining your suitability for the role, salary expectations and notice period. Please note that we will need to establish your right to work during the recruitment process.
Company description: Thornton & Ross Job description: STADA UK Thornton & Ross is on an exciting growth journey with more than 700 employees being fully committed to our purpose of Caring for Peoples Health as a Trusted Partner. Together we are shaping the future of Thornton & Ross by living our values of Integrity, Entrepreneurship, Agility and One STADA click apply for full job details
May 29, 2026
Full time
Company description: Thornton & Ross Job description: STADA UK Thornton & Ross is on an exciting growth journey with more than 700 employees being fully committed to our purpose of Caring for Peoples Health as a Trusted Partner. Together we are shaping the future of Thornton & Ross by living our values of Integrity, Entrepreneurship, Agility and One STADA click apply for full job details
QC Analyst page is loaded QC Analystremote type: Onsitelocations: Grangemouth,SCtime type: Full timeposted on: Posted Todaytime left to apply: End Date: May 26, 2026 (27 days left to apply)job requisition id: R Be the First to Apply Division Piramal Pharma SolutionsPiramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide. For more details, please visit :Job TitleQC AnalystJob DescriptionTo execute defined and trained Quality Control department tests for the release of raw materials, in process products, bulk drug substance, final products and stability products according to defined procedures and protocols and according with best cGMP work practices, Quality standards and metricsKey Roles/Responsibilities: Perform batch disposition and stability activities in a proactive and timely manner which includes Quality Control testing and reporting of raw materials, in process, bulk drug substance, final products and stability products to GMP and in accordance with Annex 11 Computerised Systems and 21CFRpart11 Good Documentation Practices for Electronic Data. Perform stability study programme activities, storage of in process, and final products samples and retention sample management System owners of QC equipment, assisting in equipment periodic reviews, monitoring and maintaining calibration status of equipment within the Quality Control department. Ownership and accountability of deviations, investigations and laboratory investigations and timely completion of these documents Preparation and update of SOPs, instructions and protocols and other Quality Control documentation Checking and reviewing of data in compliance with Data Integrity requirements Actively contribute to department and site audit readiness requirements including any continuous improvement initiatives. Calibration of equipment and instruments used to perform QC testing and informing relevant personnel in a timely manner of any failure of calibration Maintain Quality Control information systems Maintain a technical ability, knowledge and understanding of relevant regulatory requirements for GMP, safety and environmental policies required in order to perform role as QC Analyst Assist in investigation of quality incidents and other problem solving forums and complete QMS documentation in a timely manner. Attend internal and external scientific and technical meetings and conferences where appropriate Carry out general maintenance and house keeping of equipment and laboratories Available to provide cover for other departments within the organisation as required Available to undertake any other duties as requested by the QC Manager in accordance with Company requirementsCompetencies: Attention to detail reliability effective communicationunderstanding of scientific and technical processes Get In TouchIntroduce yourself to our recruiters and we'll get in touch if there's a role that seems like a good match.PPL provides equal employment opportunities to all employees and applicants for employment. It prohibits discrimination and harassment based on race, color, age, sex, religion, national origin or ethnicity, disability status, genetics, protected veteran status, sexual orientation, gender identity, or expression, or any other characteristic protected by applicable law.Our employment decisions are based on merit considering qualifications, skills, performance, and achievements. Equal employment opportunity applies to all terms and conditions of employment, including recruitment, selection, training, social programs, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions.
May 29, 2026
Full time
QC Analyst page is loaded QC Analystremote type: Onsitelocations: Grangemouth,SCtime type: Full timeposted on: Posted Todaytime left to apply: End Date: May 26, 2026 (27 days left to apply)job requisition id: R Be the First to Apply Division Piramal Pharma SolutionsPiramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide. For more details, please visit :Job TitleQC AnalystJob DescriptionTo execute defined and trained Quality Control department tests for the release of raw materials, in process products, bulk drug substance, final products and stability products according to defined procedures and protocols and according with best cGMP work practices, Quality standards and metricsKey Roles/Responsibilities: Perform batch disposition and stability activities in a proactive and timely manner which includes Quality Control testing and reporting of raw materials, in process, bulk drug substance, final products and stability products to GMP and in accordance with Annex 11 Computerised Systems and 21CFRpart11 Good Documentation Practices for Electronic Data. Perform stability study programme activities, storage of in process, and final products samples and retention sample management System owners of QC equipment, assisting in equipment periodic reviews, monitoring and maintaining calibration status of equipment within the Quality Control department. Ownership and accountability of deviations, investigations and laboratory investigations and timely completion of these documents Preparation and update of SOPs, instructions and protocols and other Quality Control documentation Checking and reviewing of data in compliance with Data Integrity requirements Actively contribute to department and site audit readiness requirements including any continuous improvement initiatives. Calibration of equipment and instruments used to perform QC testing and informing relevant personnel in a timely manner of any failure of calibration Maintain Quality Control information systems Maintain a technical ability, knowledge and understanding of relevant regulatory requirements for GMP, safety and environmental policies required in order to perform role as QC Analyst Assist in investigation of quality incidents and other problem solving forums and complete QMS documentation in a timely manner. Attend internal and external scientific and technical meetings and conferences where appropriate Carry out general maintenance and house keeping of equipment and laboratories Available to provide cover for other departments within the organisation as required Available to undertake any other duties as requested by the QC Manager in accordance with Company requirementsCompetencies: Attention to detail reliability effective communicationunderstanding of scientific and technical processes Get In TouchIntroduce yourself to our recruiters and we'll get in touch if there's a role that seems like a good match.PPL provides equal employment opportunities to all employees and applicants for employment. It prohibits discrimination and harassment based on race, color, age, sex, religion, national origin or ethnicity, disability status, genetics, protected veteran status, sexual orientation, gender identity, or expression, or any other characteristic protected by applicable law.Our employment decisions are based on merit considering qualifications, skills, performance, and achievements. Equal employment opportunity applies to all terms and conditions of employment, including recruitment, selection, training, social programs, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions.
Piramal Pharma Limited in Grangemouth is seeking a QC Analyst to execute quality control tests for raw materials and finished products in compliance with best practices and regulatory standards. Responsibilities include performing stability studies, managing QC documentation, checking data integrity, and ensuring audit readiness. Candidates should demonstrate attention to detail, effective communication skills, and a reliable work ethic, along with an understanding of GMP and safety policies.
May 29, 2026
Full time
Piramal Pharma Limited in Grangemouth is seeking a QC Analyst to execute quality control tests for raw materials and finished products in compliance with best practices and regulatory standards. Responsibilities include performing stability studies, managing QC documentation, checking data integrity, and ensuring audit readiness. Candidates should demonstrate attention to detail, effective communication skills, and a reliable work ethic, along with an understanding of GMP and safety policies.
The Front Office Services Accounting team is responsible for supporting the investment accounting function within the OMS platform, ensuring accurate book of record to support valuations, performance and financial reporting across portfolios. This role sits between operations, performance, and technology, often acting as a key SME for Order Management System (OMS) Accounting. Accounting Responsible for OMS accounting, ensuring all deliverables met Responsible for Quality Control (QC) review and resolution, ensuring funds can be published in a timely manner Production of metrics on agreed frequencies Work with vendor to enhance logic and reduce breaks / QCs where appropriate Collaborate with cross-functional teams to enhance service offerings and drive innovation in accounting practices. Agree and implement SLDs in conjunction with Client, Performance and Reporting teams Understand the month end close cycle for each fund/group and the inter-dependencies that could impact Performance and Attribution Work on process improvements and ensure solutions are in place to remediate issues at the root cause Drive process improvements and innovations by leveraging analytical skills to enhance operational efficiency Publish metrics on agreed frequencies and hold regular calls to review Reconciliations Responsible for OMS reconciliations, ensuring all deliverables met Responsible for daily reconciliations of cash and stock to custodians and Middle Office Work with Cash Team on production of safe cash figure for Portfolio Managers Work with Middle Office teams to track claims in respect of failed trades / failed income Oversee tax reclaims and closing of receivables upon payment Track aged items and perform root cause analysis Exercises own judgement and collaborates with multiple internal and external stakeholders to resolve reconciliations of accounts for complex or atypical transactions Drive process improvements and innovations by leveraging analytical skills to enhance operational efficiency Spearheads Reconciliation function projects, including Platform migration, new Client Adoption etc Develop and implement processes and controls to ensure accuracy and efficiency in service delivery, aligning with BNY's strategic objectives. Stakeholder Management Partner with: Client Front Office (Oversight team / Portfolio Managers) Front Office Operations Middle Office Performance Reporting External vendors Provide insight on: P&L drivers Accounting impacts on performance Provide strategic insights and recommendations to senior management to support decision-making. Key Responsibilities Maintain accurate positions, cash, and book cost within client's OMS Ensure correct treatment of: Bonds (incl. accruals, amortisation) Equities Derivatives (swaps, FX, futures) Monitortdaily, monthly and quarterly quality control and accounting publication Responsible for resolution of any issues which materialise and ensure timely closure in alignment with Service Level Agreements Own resolution of: Cash and position breaks Pricing discrepancies Exercise own judgement and collaborates with multiple internal and external stakeholders to resolve reconciliations of accounts for complex or atypical transactions Review data and assist in resolving escalated problems that may arise during the normal daily, weekly or monthly accounting and reporting. Escalate and manage material issues impacting P&L/NAV Ensure strong control framework and QC sign-offs Work closely with Data Management and Pricing teams to ensure all data and pricing captured timely and accurately Drive resolution of any discrepancies Mentor and develop junior analysts Review work and provide technical guidance Drive: Continuous improvement in processes Platform optimisation Automation initiatives Data model improvements Influence roadmap with internal tech teams / vendors Required Skills & Experience Strong experience in: Investment accounting (multi-asset) OMS Accounting (eg Aladdin or Bloomberg IBOR platforms) Proven track record of delivery Strong understanding of: Data architecture Controls & governance NAV lifecycle Strong analytical and problem-solving capability Solid understanding of: Fixed income & derivatives Soft Skills Excellent analytical and problem-solving abilities. Ability to investigate complex breaks Comfortable dealing with front office queries Effective communication and interpersonal skills. Strong leadership and team management skills.
May 29, 2026
Full time
The Front Office Services Accounting team is responsible for supporting the investment accounting function within the OMS platform, ensuring accurate book of record to support valuations, performance and financial reporting across portfolios. This role sits between operations, performance, and technology, often acting as a key SME for Order Management System (OMS) Accounting. Accounting Responsible for OMS accounting, ensuring all deliverables met Responsible for Quality Control (QC) review and resolution, ensuring funds can be published in a timely manner Production of metrics on agreed frequencies Work with vendor to enhance logic and reduce breaks / QCs where appropriate Collaborate with cross-functional teams to enhance service offerings and drive innovation in accounting practices. Agree and implement SLDs in conjunction with Client, Performance and Reporting teams Understand the month end close cycle for each fund/group and the inter-dependencies that could impact Performance and Attribution Work on process improvements and ensure solutions are in place to remediate issues at the root cause Drive process improvements and innovations by leveraging analytical skills to enhance operational efficiency Publish metrics on agreed frequencies and hold regular calls to review Reconciliations Responsible for OMS reconciliations, ensuring all deliverables met Responsible for daily reconciliations of cash and stock to custodians and Middle Office Work with Cash Team on production of safe cash figure for Portfolio Managers Work with Middle Office teams to track claims in respect of failed trades / failed income Oversee tax reclaims and closing of receivables upon payment Track aged items and perform root cause analysis Exercises own judgement and collaborates with multiple internal and external stakeholders to resolve reconciliations of accounts for complex or atypical transactions Drive process improvements and innovations by leveraging analytical skills to enhance operational efficiency Spearheads Reconciliation function projects, including Platform migration, new Client Adoption etc Develop and implement processes and controls to ensure accuracy and efficiency in service delivery, aligning with BNY's strategic objectives. Stakeholder Management Partner with: Client Front Office (Oversight team / Portfolio Managers) Front Office Operations Middle Office Performance Reporting External vendors Provide insight on: P&L drivers Accounting impacts on performance Provide strategic insights and recommendations to senior management to support decision-making. Key Responsibilities Maintain accurate positions, cash, and book cost within client's OMS Ensure correct treatment of: Bonds (incl. accruals, amortisation) Equities Derivatives (swaps, FX, futures) Monitortdaily, monthly and quarterly quality control and accounting publication Responsible for resolution of any issues which materialise and ensure timely closure in alignment with Service Level Agreements Own resolution of: Cash and position breaks Pricing discrepancies Exercise own judgement and collaborates with multiple internal and external stakeholders to resolve reconciliations of accounts for complex or atypical transactions Review data and assist in resolving escalated problems that may arise during the normal daily, weekly or monthly accounting and reporting. Escalate and manage material issues impacting P&L/NAV Ensure strong control framework and QC sign-offs Work closely with Data Management and Pricing teams to ensure all data and pricing captured timely and accurately Drive resolution of any discrepancies Mentor and develop junior analysts Review work and provide technical guidance Drive: Continuous improvement in processes Platform optimisation Automation initiatives Data model improvements Influence roadmap with internal tech teams / vendors Required Skills & Experience Strong experience in: Investment accounting (multi-asset) OMS Accounting (eg Aladdin or Bloomberg IBOR platforms) Proven track record of delivery Strong understanding of: Data architecture Controls & governance NAV lifecycle Strong analytical and problem-solving capability Solid understanding of: Fixed income & derivatives Soft Skills Excellent analytical and problem-solving abilities. Ability to investigate complex breaks Comfortable dealing with front office queries Effective communication and interpersonal skills. Strong leadership and team management skills.
QC Lab Analyst When registering to this job board you will be redirected to the online application form. Please ensure that this is completed in full in order that your application can be reviewed. We are seeking a QC Laboratory Analyst to support the delivery of a high-quality control service for our internal and external customers. In this role, you will be responsible for managing daily laboratory tasks, prioritising effectively to ensure accuracy, compliance, and timely results. What you will be doing: Receiving and processing samples, determining the required analyses by referring to worksheets or SAP. Conducting testing in line with work instructions, maintaining accuracy, organisation, and attention to detail. Ensuring all activities are carried out in accordance with Company Health & Safety standards and relevant Risk Assessments. Recording and reporting analysis results accurately using forms, spreadsheets, phone, or SAP. Maintaining a clean and well-organised laboratory environment, supporting good housekeeping practices. Monitoring consumables, solutions, and chemical stock levels, escalating to supervisors when re-stocking is required. Reporting equipment issues promptly to ensure smooth laboratory operations. This role offers the opportunity to work in a dynamic team environment, where precision and reliability are key to supporting our business and customer needs. What We Are Looking For: To be successful in this role you will be competent in: All routine quality control chemical testing off Malted Ingredient samples in order of priority. All routine quality control testing of Malt samples in order of priority. Testing of Chemical Proficiency scheme samples. Ensuring that all internal standards and daily control malt results are monitored and if out of range escalated to lab supervisors. Supporting non routine lab tasks such as micromalt analysis Investigation of non-conforming results and updating lab supervisors in a timely manner of any outcomes including corrective actions. Routine laboratory calibration work according to the weekly and monthly schedules. Testing of non-routine samples from various production areas and NPD General maintenance of specialised equipment e.g. reagent tube changes on Nitrogen analysers. Reviewing and suggest updates to work instructions when required. Training Junior analysts on tasks 1-10 Key Behaviours and Competencies: Team Collaboration : Actively contributes to team working and cooperates with others, fostering a collaborative environment. Task Management: Ensures tasks and activities stay on track by promptly raising any issues or concerns. Problem Identification and Escalation: Identifies problems and opportunities and escalates them to the appropriate channels for resolution. Alignment with Company Values: Demonstrates adherence to the company's values and aligns their actions and behaviours. Respectful and Welcoming: Promotes a welcoming environment, treating everyone equally, fairly, and with respect. Proactive and Positive Attitude: Exhibits a proactive, positive, and can-do attitude towards tasks and challenges. Working hours: 2 shift / 7 day or 2 shift / 5 day Looking for your next challenge at Muntons? We offer a supportive environment where your skills and expertise will be valued and developed. If you are driven by challenges and eager to contribute to a team that values quality and continuous improvement, the QC Laboratory is looking for you!
May 27, 2026
Full time
QC Lab Analyst When registering to this job board you will be redirected to the online application form. Please ensure that this is completed in full in order that your application can be reviewed. We are seeking a QC Laboratory Analyst to support the delivery of a high-quality control service for our internal and external customers. In this role, you will be responsible for managing daily laboratory tasks, prioritising effectively to ensure accuracy, compliance, and timely results. What you will be doing: Receiving and processing samples, determining the required analyses by referring to worksheets or SAP. Conducting testing in line with work instructions, maintaining accuracy, organisation, and attention to detail. Ensuring all activities are carried out in accordance with Company Health & Safety standards and relevant Risk Assessments. Recording and reporting analysis results accurately using forms, spreadsheets, phone, or SAP. Maintaining a clean and well-organised laboratory environment, supporting good housekeeping practices. Monitoring consumables, solutions, and chemical stock levels, escalating to supervisors when re-stocking is required. Reporting equipment issues promptly to ensure smooth laboratory operations. This role offers the opportunity to work in a dynamic team environment, where precision and reliability are key to supporting our business and customer needs. What We Are Looking For: To be successful in this role you will be competent in: All routine quality control chemical testing off Malted Ingredient samples in order of priority. All routine quality control testing of Malt samples in order of priority. Testing of Chemical Proficiency scheme samples. Ensuring that all internal standards and daily control malt results are monitored and if out of range escalated to lab supervisors. Supporting non routine lab tasks such as micromalt analysis Investigation of non-conforming results and updating lab supervisors in a timely manner of any outcomes including corrective actions. Routine laboratory calibration work according to the weekly and monthly schedules. Testing of non-routine samples from various production areas and NPD General maintenance of specialised equipment e.g. reagent tube changes on Nitrogen analysers. Reviewing and suggest updates to work instructions when required. Training Junior analysts on tasks 1-10 Key Behaviours and Competencies: Team Collaboration : Actively contributes to team working and cooperates with others, fostering a collaborative environment. Task Management: Ensures tasks and activities stay on track by promptly raising any issues or concerns. Problem Identification and Escalation: Identifies problems and opportunities and escalates them to the appropriate channels for resolution. Alignment with Company Values: Demonstrates adherence to the company's values and aligns their actions and behaviours. Respectful and Welcoming: Promotes a welcoming environment, treating everyone equally, fairly, and with respect. Proactive and Positive Attitude: Exhibits a proactive, positive, and can-do attitude towards tasks and challenges. Working hours: 2 shift / 7 day or 2 shift / 5 day Looking for your next challenge at Muntons? We offer a supportive environment where your skills and expertise will be valued and developed. If you are driven by challenges and eager to contribute to a team that values quality and continuous improvement, the QC Laboratory is looking for you!
QC Lab Analyst When registering to this job board you will be redirected to the online application form. Please ensure that this is completed in full in order that your application can be reviewed. We are seeking a QC Laboratory Analyst to support the delivery of a high-quality control service for our internal and external customers. In this role, you will be responsible for managing daily laboratory tasks, prioritising effectively to ensure accuracy, compliance, and timely results. What you will be doing: Receiving and processing samples, determining the required analyses by referring to worksheets or SAP. Conducting testing in line with work instructions, maintaining accuracy, organisation, and attention to detail. Ensuring all activities are carried out in accordance with Company Health & Safety standards and relevant Risk Assessments. Recording and reporting analysis results accurately using forms, spreadsheets, phone, or SAP. Maintaining a clean and well-organised laboratory environment, supporting good housekeeping practices. Monitoring consumables, solutions, and chemical stock levels, escalating to supervisors when re-stocking is required. Reporting equipment issues promptly to ensure smooth laboratory operations. This role offers the opportunity to work in a dynamic team environment, where precision and reliability are key to supporting our business and customer needs. What We Are Looking For: To be successful in this role you will be competent in: All routine quality control chemical testing off Malted Ingredient samples in order of priority. All routine quality control testing of Malt samples in order of priority. Testing of Chemical Proficiency scheme samples. Ensuring that all internal standards and daily control malt results are monitored and if out of range escalated to lab supervisors. Supporting non routine lab tasks such as micromalt analysis Investigation of non-conforming results and updating lab supervisors in a timely manner of any outcomes including corrective actions. Routine laboratory calibration work according to the weekly and monthly schedules. Testing of non-routine samples from various production areas and NPD General maintenance of specialised equipment e.g. reagent tube changes on Nitrogen analysers. Reviewing and suggest updates to work instructions when required. Training Junior analysts on tasks 1-10 Key Behaviours and Competencies: Team Collaboration : Actively contributes to team working and cooperates with others, fostering a collaborative environment. Task Management: Ensures tasks and activities stay on track by promptly raising any issues or concerns. Problem Identification and Escalation: Identifies problems and opportunities and escalates them to the appropriate channels for resolution. Alignment with Company Values: Demonstrates adherence to the company's values and aligns their actions and behaviours. Respectful and Welcoming: Promotes a welcoming environment, treating everyone equally, fairly, and with respect. Proactive and Positive Attitude: Exhibits a proactive, positive, and can-do attitude towards tasks and challenges. Working hours: 2 shift / 7 day or 2 shift / 5 day Looking for your next challenge at Muntons? We offer a supportive environment where your skills and expertise will be valued and developed. If you are driven by challenges and eager to contribute to a team that values quality and continuous improvement, the QC Laboratory is looking for you!
May 26, 2026
Full time
QC Lab Analyst When registering to this job board you will be redirected to the online application form. Please ensure that this is completed in full in order that your application can be reviewed. We are seeking a QC Laboratory Analyst to support the delivery of a high-quality control service for our internal and external customers. In this role, you will be responsible for managing daily laboratory tasks, prioritising effectively to ensure accuracy, compliance, and timely results. What you will be doing: Receiving and processing samples, determining the required analyses by referring to worksheets or SAP. Conducting testing in line with work instructions, maintaining accuracy, organisation, and attention to detail. Ensuring all activities are carried out in accordance with Company Health & Safety standards and relevant Risk Assessments. Recording and reporting analysis results accurately using forms, spreadsheets, phone, or SAP. Maintaining a clean and well-organised laboratory environment, supporting good housekeeping practices. Monitoring consumables, solutions, and chemical stock levels, escalating to supervisors when re-stocking is required. Reporting equipment issues promptly to ensure smooth laboratory operations. This role offers the opportunity to work in a dynamic team environment, where precision and reliability are key to supporting our business and customer needs. What We Are Looking For: To be successful in this role you will be competent in: All routine quality control chemical testing off Malted Ingredient samples in order of priority. All routine quality control testing of Malt samples in order of priority. Testing of Chemical Proficiency scheme samples. Ensuring that all internal standards and daily control malt results are monitored and if out of range escalated to lab supervisors. Supporting non routine lab tasks such as micromalt analysis Investigation of non-conforming results and updating lab supervisors in a timely manner of any outcomes including corrective actions. Routine laboratory calibration work according to the weekly and monthly schedules. Testing of non-routine samples from various production areas and NPD General maintenance of specialised equipment e.g. reagent tube changes on Nitrogen analysers. Reviewing and suggest updates to work instructions when required. Training Junior analysts on tasks 1-10 Key Behaviours and Competencies: Team Collaboration : Actively contributes to team working and cooperates with others, fostering a collaborative environment. Task Management: Ensures tasks and activities stay on track by promptly raising any issues or concerns. Problem Identification and Escalation: Identifies problems and opportunities and escalates them to the appropriate channels for resolution. Alignment with Company Values: Demonstrates adherence to the company's values and aligns their actions and behaviours. Respectful and Welcoming: Promotes a welcoming environment, treating everyone equally, fairly, and with respect. Proactive and Positive Attitude: Exhibits a proactive, positive, and can-do attitude towards tasks and challenges. Working hours: 2 shift / 7 day or 2 shift / 5 day Looking for your next challenge at Muntons? We offer a supportive environment where your skills and expertise will be valued and developed. If you are driven by challenges and eager to contribute to a team that values quality and continuous improvement, the QC Laboratory is looking for you!
