Job Title: HR Advisor Location: Remote/ Hybrid, based in Nottingham Salary: 28,000 - 30,500 per annum Job type: Permanent, Full Time - Monday to Friday 9am to 5:30pm Total Care Matters is a well-established provider of residential children's homes across the East Midlands, caring for young people aged 8-17. With nine homes and more on the horizon, we're committed to delivering exceptional outcomes and achieving 'Outstanding' ratings from Ofsted. We believe a thriving team is key to delivering excellent care - and you'll be part of making that happen. About the role: Do you believe every child deserves a safe, nurturing home where they can thrive, learn, and build meaningful relationships? At Total Care Matters, we share your passion - and we're growing our team. We're looking for a committed and compassionate HR Advisor to help us shape a supportive workplace culture that empowers those who care for our children. As our HR Advisor, you'll be a vital part of our friendly HR team, supporting the people strategy and providing day-to-day HR operational support. Reporting to the HR Business Partner, you'll be a trusted point of contact for managers and staff, handling employee relations, supporting performance and wellbeing, and contributing to strategic projects. Key duties: Full cycle of employee relations including absence, performance, disciplinaries, and grievances Co-ordinating safeguarding related HR processes including leading on safeguarding investigations Managing flexible working requests, maternity/paternity processes, and absence referrals (including Occupational Health) Monitoring and reporting annual leave via the HRIS system Overseeing QCF Level 3 and 5 qualifications tracking and liaising with assessors Conducting staff surveys and exit interviews and analysing feedback Working with our employment law advisors to ensure compliance across all HR activities About you: A confident communicator and advisor to staff and managers alike Highly organised with excellent attention to detail Confidence handling ER casework and advising managers at all levels. A proactive, can-do attitude and a genuine passion for supporting people. Comfortable working with HRIS, MS Office, and managing data effectively Knowledgeable in employment law and safeguarding best practices Championing initiatives that make us an employer of choice in the care sector We're looking for someone who's confident, approachable, and an excellent communicator - someone who can combine compassion with professional rigour. Benefits: Career progression & funded professional development (CIPD included) Hybrid working and flexible work culture 28 days annual leave (incl. bank holidays) Employee Assistance Programme (24/7 confidential support) Blue Light Card discounts Casual dress and supportive team culture On-site parking Health cash plan and Westfield Rewards Staff referral bonus This post is exempt from the Rehabilitation of Offenders Act 1974 and subject to an enhanced DBS Disclosure check. 'Total Care Matters Ltd. is committed to safeguarding and promoting the welfare of children and young people. To achieve our commitment, we will ensure continuous development and improvement of robust safeguarding processes and procedures that promote a culture of safeguarding amongst our workforce'. If you feel you have the necessary skills and experience to be successful in this role, click on the APPLY button to send your CV and Cover Letter for this role. Candidates with the relevant experience or job titles of: HR Advisor, HR Generalist, HR Officer, HR Analyst, HR Data Analyst, Human Resource Analyst, Senior HR Assistant, HR Adviser, Senior HR Advisor, Assistant HR Manager, HR Coordinator, Human Resource Advisor may also beconsidered for this role.
Jul 24, 2025
Full time
Job Title: HR Advisor Location: Remote/ Hybrid, based in Nottingham Salary: 28,000 - 30,500 per annum Job type: Permanent, Full Time - Monday to Friday 9am to 5:30pm Total Care Matters is a well-established provider of residential children's homes across the East Midlands, caring for young people aged 8-17. With nine homes and more on the horizon, we're committed to delivering exceptional outcomes and achieving 'Outstanding' ratings from Ofsted. We believe a thriving team is key to delivering excellent care - and you'll be part of making that happen. About the role: Do you believe every child deserves a safe, nurturing home where they can thrive, learn, and build meaningful relationships? At Total Care Matters, we share your passion - and we're growing our team. We're looking for a committed and compassionate HR Advisor to help us shape a supportive workplace culture that empowers those who care for our children. As our HR Advisor, you'll be a vital part of our friendly HR team, supporting the people strategy and providing day-to-day HR operational support. Reporting to the HR Business Partner, you'll be a trusted point of contact for managers and staff, handling employee relations, supporting performance and wellbeing, and contributing to strategic projects. Key duties: Full cycle of employee relations including absence, performance, disciplinaries, and grievances Co-ordinating safeguarding related HR processes including leading on safeguarding investigations Managing flexible working requests, maternity/paternity processes, and absence referrals (including Occupational Health) Monitoring and reporting annual leave via the HRIS system Overseeing QCF Level 3 and 5 qualifications tracking and liaising with assessors Conducting staff surveys and exit interviews and analysing feedback Working with our employment law advisors to ensure compliance across all HR activities About you: A confident communicator and advisor to staff and managers alike Highly organised with excellent attention to detail Confidence handling ER casework and advising managers at all levels. A proactive, can-do attitude and a genuine passion for supporting people. Comfortable working with HRIS, MS Office, and managing data effectively Knowledgeable in employment law and safeguarding best practices Championing initiatives that make us an employer of choice in the care sector We're looking for someone who's confident, approachable, and an excellent communicator - someone who can combine compassion with professional rigour. Benefits: Career progression & funded professional development (CIPD included) Hybrid working and flexible work culture 28 days annual leave (incl. bank holidays) Employee Assistance Programme (24/7 confidential support) Blue Light Card discounts Casual dress and supportive team culture On-site parking Health cash plan and Westfield Rewards Staff referral bonus This post is exempt from the Rehabilitation of Offenders Act 1974 and subject to an enhanced DBS Disclosure check. 'Total Care Matters Ltd. is committed to safeguarding and promoting the welfare of children and young people. To achieve our commitment, we will ensure continuous development and improvement of robust safeguarding processes and procedures that promote a culture of safeguarding amongst our workforce'. If you feel you have the necessary skills and experience to be successful in this role, click on the APPLY button to send your CV and Cover Letter for this role. Candidates with the relevant experience or job titles of: HR Advisor, HR Generalist, HR Officer, HR Analyst, HR Data Analyst, Human Resource Analyst, Senior HR Assistant, HR Adviser, Senior HR Advisor, Assistant HR Manager, HR Coordinator, Human Resource Advisor may also beconsidered for this role.
QC Supervisor Competitive Salary + Benefits Wrexham Days Only gap technical are proud to be representing this global manufacturing business in their search for a QC Section Leader to work at their facility based near Wrexham Performance Objectives To manage the analytical testing of solid dose products. To ensure that all testing is carried out within the requirements of cGMP, Health and Safety and COSHH. To critically review analytical data, and where specifications are met, approve products for further processing. In this role, you will be responsible for leading a team of analyst and ensuring that release of our product meet the highest standards of quality and consistency. You will be a key player in driving continuous improvement and ensuring compliance with industry regulation and company polices. Person Specification Science degree in Chemistry or equivalent qualification. Previous experience within a pharmaceutical or equivalent laboratory environment is essential. A thorough understanding of current GMP, Health and Safety and COSHH regulation and sound supervisory and interpersonal skills. Manage the workload of the QC solid dose team, including preparing weekly and daily work schedules. Previous experience in leading OOS/OOT investigations and deviations is essential. Previous experience in leading a team is preferred. Previous experience in representing the QC group at internal, customer and regulatory audits and liaising with the regulatory affair department is essential Experience in leading the analytical method transfer, verification and validation is preferred Apply Please send your CV via the Apply now option on the website If you have any questions or are interested in any other opportunities we may have, please do not hesitate to get in touch This vacancy is being advertised on behalf of gap technical who are operating as an employment agency. gap technical are committed to the selection, recruitment and development of the best people, basing judgements solely on suitability for the job. Closing Date: 24/08/2025 "By applying for the above position and providing your personal data to us you understand that your data will be processed in line with our Privacy Policy."
Jul 24, 2025
Full time
QC Supervisor Competitive Salary + Benefits Wrexham Days Only gap technical are proud to be representing this global manufacturing business in their search for a QC Section Leader to work at their facility based near Wrexham Performance Objectives To manage the analytical testing of solid dose products. To ensure that all testing is carried out within the requirements of cGMP, Health and Safety and COSHH. To critically review analytical data, and where specifications are met, approve products for further processing. In this role, you will be responsible for leading a team of analyst and ensuring that release of our product meet the highest standards of quality and consistency. You will be a key player in driving continuous improvement and ensuring compliance with industry regulation and company polices. Person Specification Science degree in Chemistry or equivalent qualification. Previous experience within a pharmaceutical or equivalent laboratory environment is essential. A thorough understanding of current GMP, Health and Safety and COSHH regulation and sound supervisory and interpersonal skills. Manage the workload of the QC solid dose team, including preparing weekly and daily work schedules. Previous experience in leading OOS/OOT investigations and deviations is essential. Previous experience in leading a team is preferred. Previous experience in representing the QC group at internal, customer and regulatory audits and liaising with the regulatory affair department is essential Experience in leading the analytical method transfer, verification and validation is preferred Apply Please send your CV via the Apply now option on the website If you have any questions or are interested in any other opportunities we may have, please do not hesitate to get in touch This vacancy is being advertised on behalf of gap technical who are operating as an employment agency. gap technical are committed to the selection, recruitment and development of the best people, basing judgements solely on suitability for the job. Closing Date: 24/08/2025 "By applying for the above position and providing your personal data to us you understand that your data will be processed in line with our Privacy Policy."
Job Title: Analyst - Regulatory Information Management Location: Marlow Contract: 12 Months / Hybrid 3 days onsite Hours: 37.5 hours per week Rates: 23 p/h Job Description SRG are looking for an analyst - regulatory information management for a leading pharmaceutical company based in Marlow. As part of this role, you will be supporting process improvement initiatives. Support structured data submissions and all related tasks, including xEVMPD, SPOR and IDMP implementation. Support Regulatory Information Management (RIM) globally, focusing on key systems and processes, including COSMOS (RIM system) Supports Data enrichment and archiving remediation initiatives. Work with members of the Regulatory Lifecycle Management team to share knowledge and improve RIM processes. Build and maintains relationships with Regulatory and other staff within and outside of the region to ensure effective communication and efficient implementation of regulatory information management. Duties and Responsibilities Subject to internal QC audit, ensure all data submissions and related reference/master data are managed accurately and in accordance with SOPs. Establish relationships with 'in-country' teams and global regulatory teams to ensure that they are aware of how data submissions are managed. Maintain awareness of International regulatory procedures and how any changes may impact reference and master data management within the Regulatory Information Management system. Work with other Local System Administrators to suggest, discuss and implement system and process improvements in line with regulatory changes and as part of a quality management cycle, subject to Global Data Council representations and approvals. Work with global BTS to implement system upgrades and other improvements. Qualify requests and run accurate reports and queries as requested. Maintain compliance with departmental SOPs and Work Instructions. Experience and Qualifications Graduate (preferably in a Life Science or IT related discipline), or equivalent/relevant experience. Knowledge of Regulatory Business Processes / Pharma and/or Medical Devices R&D Business Regulatory Systems and Database experience (Liquent, Veeva, CARA or similar) Some knowledge of European Regulatory Procedures (Centralised, Decentralised and Mutual Recognition) Some knowledge of Regulatory Submission types (MAAs, Variations, Renewals, CTAs, DSURs etc) Knowledge of EMA Platforms preferred (IDMP, XEVMPD, SPOR, CTIS, IRIS) Essential Skills and Abilities Organisational and planning ability Excellent written, verbal and interpersonal skills Ability to work effectively and collaboratively across cultures and cross-functionally Ability to identify compliance risks and escalate when necessary Ability to multitask, prioritize, and manage multiple projects and deadlines Sense of personal responsibility and accountability Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
Jul 23, 2025
Seasonal
Job Title: Analyst - Regulatory Information Management Location: Marlow Contract: 12 Months / Hybrid 3 days onsite Hours: 37.5 hours per week Rates: 23 p/h Job Description SRG are looking for an analyst - regulatory information management for a leading pharmaceutical company based in Marlow. As part of this role, you will be supporting process improvement initiatives. Support structured data submissions and all related tasks, including xEVMPD, SPOR and IDMP implementation. Support Regulatory Information Management (RIM) globally, focusing on key systems and processes, including COSMOS (RIM system) Supports Data enrichment and archiving remediation initiatives. Work with members of the Regulatory Lifecycle Management team to share knowledge and improve RIM processes. Build and maintains relationships with Regulatory and other staff within and outside of the region to ensure effective communication and efficient implementation of regulatory information management. Duties and Responsibilities Subject to internal QC audit, ensure all data submissions and related reference/master data are managed accurately and in accordance with SOPs. Establish relationships with 'in-country' teams and global regulatory teams to ensure that they are aware of how data submissions are managed. Maintain awareness of International regulatory procedures and how any changes may impact reference and master data management within the Regulatory Information Management system. Work with other Local System Administrators to suggest, discuss and implement system and process improvements in line with regulatory changes and as part of a quality management cycle, subject to Global Data Council representations and approvals. Work with global BTS to implement system upgrades and other improvements. Qualify requests and run accurate reports and queries as requested. Maintain compliance with departmental SOPs and Work Instructions. Experience and Qualifications Graduate (preferably in a Life Science or IT related discipline), or equivalent/relevant experience. Knowledge of Regulatory Business Processes / Pharma and/or Medical Devices R&D Business Regulatory Systems and Database experience (Liquent, Veeva, CARA or similar) Some knowledge of European Regulatory Procedures (Centralised, Decentralised and Mutual Recognition) Some knowledge of Regulatory Submission types (MAAs, Variations, Renewals, CTAs, DSURs etc) Knowledge of EMA Platforms preferred (IDMP, XEVMPD, SPOR, CTIS, IRIS) Essential Skills and Abilities Organisational and planning ability Excellent written, verbal and interpersonal skills Ability to work effectively and collaboratively across cultures and cross-functionally Ability to identify compliance risks and escalate when necessary Ability to multitask, prioritize, and manage multiple projects and deadlines Sense of personal responsibility and accountability Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
Quality Control Analyst - Your future role? As a Quality Control Analyst in Ashford, you will evaluate raw materials, intermediates, and finished goods by performing basic sensory or physical or analytical tests to secure compliance with product safety regulations, specifications, and standards. This role reports to the Quality Control Manager. You will: Perform a variety of quality control-related sensory assessments including organoleptic (e.g. odor & taste) and visual determinations (e.g. color and appearance). Perform a variety of quality control-related measurements (e.g. chemical tests to determine pH, and acid values) using wet chemical methods such as titration, saponification. Perform a variety of quality control-related measurements (e.g. specific gravity, refractive index, melting point, flashpoint) to determine the physical characteristics of the sample Perform a variety of quality control-related measurements (e.g. chromatography, GC-MS, infra-red, ICP) to determine the composition of samples tested. Enter results into laboratory books/systems such as SAP. Document non-conformance. Extract, summarise, and collect data for material-related investigations. Your professional background: High School Diploma within a technical field such as Chemistry, Biology, etc. with experience in chemistry or laboratory techniques and general equivalency development (GED) is required. Overall work experience of 1 to 2 years in a similar position. Previous background in Sensory Evaluation and Analytical QC. Laboratory or QC techniques. Good computer knowledge with such systems as SAP, Databases, and Microsoft Office products. Operational experience in a laboratory environment, analytical equipment, and instruments such as weighing balance, Densitometer, Refractometer, Moisture balances, Karl Fischer Titrator, Sieve testing equipment, and GC. Knowledge of chemical substances, hazardous materials, and related local regulations. Basic Sensory evaluation capability / potential capability preferred.
Jul 23, 2025
Seasonal
Quality Control Analyst - Your future role? As a Quality Control Analyst in Ashford, you will evaluate raw materials, intermediates, and finished goods by performing basic sensory or physical or analytical tests to secure compliance with product safety regulations, specifications, and standards. This role reports to the Quality Control Manager. You will: Perform a variety of quality control-related sensory assessments including organoleptic (e.g. odor & taste) and visual determinations (e.g. color and appearance). Perform a variety of quality control-related measurements (e.g. chemical tests to determine pH, and acid values) using wet chemical methods such as titration, saponification. Perform a variety of quality control-related measurements (e.g. specific gravity, refractive index, melting point, flashpoint) to determine the physical characteristics of the sample Perform a variety of quality control-related measurements (e.g. chromatography, GC-MS, infra-red, ICP) to determine the composition of samples tested. Enter results into laboratory books/systems such as SAP. Document non-conformance. Extract, summarise, and collect data for material-related investigations. Your professional background: High School Diploma within a technical field such as Chemistry, Biology, etc. with experience in chemistry or laboratory techniques and general equivalency development (GED) is required. Overall work experience of 1 to 2 years in a similar position. Previous background in Sensory Evaluation and Analytical QC. Laboratory or QC techniques. Good computer knowledge with such systems as SAP, Databases, and Microsoft Office products. Operational experience in a laboratory environment, analytical equipment, and instruments such as weighing balance, Densitometer, Refractometer, Moisture balances, Karl Fischer Titrator, Sieve testing equipment, and GC. Knowledge of chemical substances, hazardous materials, and related local regulations. Basic Sensory evaluation capability / potential capability preferred.
Quality Analyst Location: Nottingham Department: QC Lab Employment Type: Full-Time Hours of work- Monday- Friday 8AM: 4PM Pay Rate- 12.60 per hour Job Summary: We are seeking a detail-oriented and skilled Quality Analyst to join our packaging team. The Quality Analyst will be responsible for conducting quality testing, analysing data, and reporting findings. This role requires adherence to strict quality standards to ensure accurate and reliable results, contributing to the continuous improvement of our processes and products. Key Responsibilities: Quality Testing: Perform quality testing on products, processes, or services using standard testing methods and protocols. Data Analysis: Collect, analyse, and interpret data to assess quality performance and identify areas for improvement. Documentation: Record and report test results accurately, maintaining thorough documentation in quality management systems. Checking incoming packaging materials against the standard, completing FTIR analysis. Quality Control: Adhere to quality control procedures to ensure consistent and reliable test outcomes. Process Improvement: Collaborate with cross-functional teams to identify, troubleshoot, and resolve quality issues, optimising procedures for better efficiency and effectiveness. Compliance Monitoring: Ensure compliance with industry standards, regulatory requirements, and internal quality policies. Audit Support: Assist in internal and external quality audits, providing necessary documentation and data. Training and Development: Participate in the training of staff on quality standards, processes, and best practices. Safety Compliance: Follow safety protocols and guidelines to maintain a safe working environment. Qualifications and Skills: Education: A degree in a Science based subject, at Bachelor's level or higher. Subjects include but are not limited to Chemistry, Pharmaceuticals, Bio-medical Science, Forensic Science and Biology. Experience: Some laboratory practical experience, either through a laboratory practical and research degree or through industry, is essential. Analytic Chemistry experience would be preferable but is not essential. Experience working in a laboratory in the industry would be preferable but not essential. Technical Knowledge: Strong understanding of quality testing methods, principles, and industry standards. Computer literate. Data Proficiency: Familiarity with data analysis tools and quality management software. Attention to Detail: Excellent attention to detail and organisational skills. Communication: Effective written and verbal communication skills. Problem-Solving: Strong analytic and problem-solving abilities. Procedure Adherence: Ability to follow standard operating procedures (SOP's) and protocols. Additional Information: This position may require occasional weekend or evening work depending on project deadlines. Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer. By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explains how we will use your information - please copy and paste the following link in to your browser (url removed)
Jul 23, 2025
Seasonal
Quality Analyst Location: Nottingham Department: QC Lab Employment Type: Full-Time Hours of work- Monday- Friday 8AM: 4PM Pay Rate- 12.60 per hour Job Summary: We are seeking a detail-oriented and skilled Quality Analyst to join our packaging team. The Quality Analyst will be responsible for conducting quality testing, analysing data, and reporting findings. This role requires adherence to strict quality standards to ensure accurate and reliable results, contributing to the continuous improvement of our processes and products. Key Responsibilities: Quality Testing: Perform quality testing on products, processes, or services using standard testing methods and protocols. Data Analysis: Collect, analyse, and interpret data to assess quality performance and identify areas for improvement. Documentation: Record and report test results accurately, maintaining thorough documentation in quality management systems. Checking incoming packaging materials against the standard, completing FTIR analysis. Quality Control: Adhere to quality control procedures to ensure consistent and reliable test outcomes. Process Improvement: Collaborate with cross-functional teams to identify, troubleshoot, and resolve quality issues, optimising procedures for better efficiency and effectiveness. Compliance Monitoring: Ensure compliance with industry standards, regulatory requirements, and internal quality policies. Audit Support: Assist in internal and external quality audits, providing necessary documentation and data. Training and Development: Participate in the training of staff on quality standards, processes, and best practices. Safety Compliance: Follow safety protocols and guidelines to maintain a safe working environment. Qualifications and Skills: Education: A degree in a Science based subject, at Bachelor's level or higher. Subjects include but are not limited to Chemistry, Pharmaceuticals, Bio-medical Science, Forensic Science and Biology. Experience: Some laboratory practical experience, either through a laboratory practical and research degree or through industry, is essential. Analytic Chemistry experience would be preferable but is not essential. Experience working in a laboratory in the industry would be preferable but not essential. Technical Knowledge: Strong understanding of quality testing methods, principles, and industry standards. Computer literate. Data Proficiency: Familiarity with data analysis tools and quality management software. Attention to Detail: Excellent attention to detail and organisational skills. Communication: Effective written and verbal communication skills. Problem-Solving: Strong analytic and problem-solving abilities. Procedure Adherence: Ability to follow standard operating procedures (SOP's) and protocols. Additional Information: This position may require occasional weekend or evening work depending on project deadlines. Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer. By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explains how we will use your information - please copy and paste the following link in to your browser (url removed)
Social network you want to login/join with: Ready to be pushed beyond what you think you're capable of? At Coinbase, our mission is to increase economic freedom in the world. It's a massive, ambitious opportunity that demands the best of us, every day, as we build the emerging onchain platform - and with it, the future global financial system. To achieve our mission, we're seeking a very specific candidate. We want someone who is passionate about our mission and who believes in the power of crypto and blockchain technology to update the financial system. We want someone who is eager to leave their mark on the world, who relishes the pressure and privilege of working with high caliber colleagues, and who actively seeks feedback to keep leveling up. We want someone who will run towards, not away from, solving the company's hardest problems. Our is intense and isn't for everyone. But if you want to build the future alongside others who excel in their disciplines and expect the same from you, there's no better place to be. While many roles at Coinbase are remote-first, we are not remote-only. In-person participation is required throughout the year. Team and company-wide offsites are held multiple times annually to foster collaboration, connection, and alignment. Attendance is expected and fully supported. Coinbase is committed to preventing illicit activities on our platform, safeguarding against criminal exploitation, and ensuring full compliance with legal and regulatory standards. As the Associate Manager for the International Escalations & TMS L1 QA Programs, you will play a pivotal role in supporting Coinbase's AML/CFT (Anti-Money Laundering/Combating the Financing of Terrorism) program. Your primary responsibility will be leading a team of Quality Assurance Experts who conduct thorough reviews of international investigations. What you'll be doing (ie. job duties): Oversee the Transactions Monitoring System (TMS) Quality Assurance Programs for International Escalations and TMS Level 1 Reviews. Manage a team of Senior Quality Assurance Analysts Conduct weekly capacity planning reviews and allocate cases for auditing based on analyst capacity Establish, maintain and enhance QA metrics and Standard Operating Procedures Partnering with Operations on initiatives to improve output, quality metrics and key risk indicators Perform Root Cause Analysis to surface underlying systemic drivers of persistent opportunity areas of improvement Assist with compliance, internal audit or regulatory, Design Effectiveness Assessments and Operational Effectiveness Testing of relevant TMS Processes Ensure service level agreements and quality metrics are met for both individual and team performance. Collaborate with internal teams, including Data Analytics, Escalations, Financial Crime Compliance, and Learning & Development to launch or improve workflows and processes Utilize a deep understanding of metrics to drive data-driven recommendations Continuously add value through effective impact analysis, prioritization, and efficient project execution Conduct post-implementation reviews and suggest process revisions as necessary Ensure comprehensive change communication and coordination Identify and implement process optimization opportunities to enhance efficiency and eliminate roadblocks Handle ad-hoc assignments as required What we look for in you (ie. job requirements): An ideal candidate would have 6+ years BSA/AML experience with high quality technical expertise at an equivalent financial services organization, fintech or advisory firm, regulator or law enforcement agency A professional compliance qualification is a must (ICA, ACAMS or equivalent) Strong communication skills and presence: ability to interface with regulators and executive teams Motivated by Coinbase's mission and crafting a seamless support experience for our global customer base Experience in project management and process improvements Flexible and adaptable to meeting the evolving needs of a high-growth and fast paced organisation Strong planning skills; able to manage multiple priorities and tasks Travel requirements up to 10% to Coinbase offices and vendor locations Strong Data Analytics knowledge (Excel or Google Sheets) Nice to haves: Knowledgeable in the area of virtual currencies, particularly in the context of AML/CTF Knowledge of blockchain analytics tools Experience in performing QC and/or QA Advanced understanding of Google apps, JIRA, Salesforce Service Cloud P71167 Pay Transparency Notice: The target annual salary for this position can range as detailed below. Full time offers from Coinbase also include target bonus + target equity + benefits (including medical, dental, and vision). Pay Range:£81,900-£81,900 GBP Please be advised that each candidate may submit a maximum of four applications within any 30-day period. We encourage you to carefully evaluate how your skills and interests align with Coinbase's roles before applying. Commitment to Equal Opportunity Coinbase is committed to diversity in its workforce and is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, sex, gender expression or identity, sexual orientation or any other basis protected by applicable law. Coinbase will also consider for employment qualified applicants with criminal histories in a manner consistent with applicable federal, state and local law. For US applicants, you may view the Know Your Rights notice . Additionally, Coinbase participates in the in certain locations, as required by law. Coinbase is also committed to providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation because of a disability for any part of the employment process, please contact us at accommodations at to let us know the nature of your request and your contact information. For quick access to screen reading technology compatible with this site a free compatible screen reader . Global Data Privacy Notice for Job Candidates and Applicants Depending on your location, the General Data Protection Regulation (GDPR) and California Consumer Privacy Act (CCPA) may regulate the way we manage the data of job applicants. Our full notice outlining how data will be processed as part of the application procedure for applicable locations is available . By submitting your application, you are agreeing to our use and processing of your data as required. For US applicants only, by submitting your application you are agreeing to arbitration of disputes as outlined
Jul 23, 2025
Full time
Social network you want to login/join with: Ready to be pushed beyond what you think you're capable of? At Coinbase, our mission is to increase economic freedom in the world. It's a massive, ambitious opportunity that demands the best of us, every day, as we build the emerging onchain platform - and with it, the future global financial system. To achieve our mission, we're seeking a very specific candidate. We want someone who is passionate about our mission and who believes in the power of crypto and blockchain technology to update the financial system. We want someone who is eager to leave their mark on the world, who relishes the pressure and privilege of working with high caliber colleagues, and who actively seeks feedback to keep leveling up. We want someone who will run towards, not away from, solving the company's hardest problems. Our is intense and isn't for everyone. But if you want to build the future alongside others who excel in their disciplines and expect the same from you, there's no better place to be. While many roles at Coinbase are remote-first, we are not remote-only. In-person participation is required throughout the year. Team and company-wide offsites are held multiple times annually to foster collaboration, connection, and alignment. Attendance is expected and fully supported. Coinbase is committed to preventing illicit activities on our platform, safeguarding against criminal exploitation, and ensuring full compliance with legal and regulatory standards. As the Associate Manager for the International Escalations & TMS L1 QA Programs, you will play a pivotal role in supporting Coinbase's AML/CFT (Anti-Money Laundering/Combating the Financing of Terrorism) program. Your primary responsibility will be leading a team of Quality Assurance Experts who conduct thorough reviews of international investigations. What you'll be doing (ie. job duties): Oversee the Transactions Monitoring System (TMS) Quality Assurance Programs for International Escalations and TMS Level 1 Reviews. Manage a team of Senior Quality Assurance Analysts Conduct weekly capacity planning reviews and allocate cases for auditing based on analyst capacity Establish, maintain and enhance QA metrics and Standard Operating Procedures Partnering with Operations on initiatives to improve output, quality metrics and key risk indicators Perform Root Cause Analysis to surface underlying systemic drivers of persistent opportunity areas of improvement Assist with compliance, internal audit or regulatory, Design Effectiveness Assessments and Operational Effectiveness Testing of relevant TMS Processes Ensure service level agreements and quality metrics are met for both individual and team performance. Collaborate with internal teams, including Data Analytics, Escalations, Financial Crime Compliance, and Learning & Development to launch or improve workflows and processes Utilize a deep understanding of metrics to drive data-driven recommendations Continuously add value through effective impact analysis, prioritization, and efficient project execution Conduct post-implementation reviews and suggest process revisions as necessary Ensure comprehensive change communication and coordination Identify and implement process optimization opportunities to enhance efficiency and eliminate roadblocks Handle ad-hoc assignments as required What we look for in you (ie. job requirements): An ideal candidate would have 6+ years BSA/AML experience with high quality technical expertise at an equivalent financial services organization, fintech or advisory firm, regulator or law enforcement agency A professional compliance qualification is a must (ICA, ACAMS or equivalent) Strong communication skills and presence: ability to interface with regulators and executive teams Motivated by Coinbase's mission and crafting a seamless support experience for our global customer base Experience in project management and process improvements Flexible and adaptable to meeting the evolving needs of a high-growth and fast paced organisation Strong planning skills; able to manage multiple priorities and tasks Travel requirements up to 10% to Coinbase offices and vendor locations Strong Data Analytics knowledge (Excel or Google Sheets) Nice to haves: Knowledgeable in the area of virtual currencies, particularly in the context of AML/CTF Knowledge of blockchain analytics tools Experience in performing QC and/or QA Advanced understanding of Google apps, JIRA, Salesforce Service Cloud P71167 Pay Transparency Notice: The target annual salary for this position can range as detailed below. Full time offers from Coinbase also include target bonus + target equity + benefits (including medical, dental, and vision). Pay Range:£81,900-£81,900 GBP Please be advised that each candidate may submit a maximum of four applications within any 30-day period. We encourage you to carefully evaluate how your skills and interests align with Coinbase's roles before applying. Commitment to Equal Opportunity Coinbase is committed to diversity in its workforce and is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, sex, gender expression or identity, sexual orientation or any other basis protected by applicable law. Coinbase will also consider for employment qualified applicants with criminal histories in a manner consistent with applicable federal, state and local law. For US applicants, you may view the Know Your Rights notice . Additionally, Coinbase participates in the in certain locations, as required by law. Coinbase is also committed to providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation because of a disability for any part of the employment process, please contact us at accommodations at to let us know the nature of your request and your contact information. For quick access to screen reading technology compatible with this site a free compatible screen reader . Global Data Privacy Notice for Job Candidates and Applicants Depending on your location, the General Data Protection Regulation (GDPR) and California Consumer Privacy Act (CCPA) may regulate the way we manage the data of job applicants. Our full notice outlining how data will be processed as part of the application procedure for applicable locations is available . By submitting your application, you are agreeing to our use and processing of your data as required. For US applicants only, by submitting your application you are agreeing to arbitration of disputes as outlined
Job Title: QC Analyst - Biosafety Location: Speke, Liverpool. Contract: 12 months Rate: 15.25 p/h (inclusive of shift uplift) Shift : 4 days on, 4 days off. 7am - 7pm. SRG are currently working with a global pharmaceutical manufacturer based in Liverpool, looking for QC Analyst (Biosafety) to join the team. The site in Speke specialises in the production of sterile injectable products, for the treatment of the flu. This is a fantastic opportunity for a Biological Science graduate with some GMP experience to further their career. Main responsibilities: Performing a range of tests within a highly regulated Quality Control laboratory to GMP regulations. Performing routine QC testing Documenting laboratory results in an accurate and timely manner. Complying with GMP regulatory requirements at all times. Key requirements: Experience of working to GMP/pharmaceutical regulatory requirements is desirable. Biological background either from university degree or relevant work in the field Computer skills, excel, word, outlook Preferrable Experience within cell cultures and/or assay testing. LIMS and SAP Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
Jul 23, 2025
Seasonal
Job Title: QC Analyst - Biosafety Location: Speke, Liverpool. Contract: 12 months Rate: 15.25 p/h (inclusive of shift uplift) Shift : 4 days on, 4 days off. 7am - 7pm. SRG are currently working with a global pharmaceutical manufacturer based in Liverpool, looking for QC Analyst (Biosafety) to join the team. The site in Speke specialises in the production of sterile injectable products, for the treatment of the flu. This is a fantastic opportunity for a Biological Science graduate with some GMP experience to further their career. Main responsibilities: Performing a range of tests within a highly regulated Quality Control laboratory to GMP regulations. Performing routine QC testing Documenting laboratory results in an accurate and timely manner. Complying with GMP regulatory requirements at all times. Key requirements: Experience of working to GMP/pharmaceutical regulatory requirements is desirable. Biological background either from university degree or relevant work in the field Computer skills, excel, word, outlook Preferrable Experience within cell cultures and/or assay testing. LIMS and SAP Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
Job Title: QC Analyst - AMB Location: Speke, Liverpool. Rate: 15.25 p/h (inclusive of shift uplift) Shift : 4 days on, 4 days off. 7am - 7pm. Contract : until end of December SRG are currently working with a global pharmaceutical manufacturer based in Liverpool, looking for QC Analyst - AMB (Analytical, Molecular and Bioassay) to join the team. The site in Speke specialises in the production of sterile injectable products, for the treatment of the flu. The successful individual will support the development & release of the latest Vaccine technologies, using a number of both chemical & biological testing methods. Key responsibilities: Perform analytical, biosafety & cell science testing on raw materials, intermediates and finished products Complete laboratory documentation accurately and in accordance with industry regulatory standards Utilise technical expertise to troubleshoot various assays as required Key requirements: Degree qualified in Chemistry, Biochemistry, Biomedical Science or a related scientific discipline Demonstrated practical experience a Prior industrial experience in a GMP regulated environment is highly desirable Strong verbal & written communication skills. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
Jul 22, 2025
Seasonal
Job Title: QC Analyst - AMB Location: Speke, Liverpool. Rate: 15.25 p/h (inclusive of shift uplift) Shift : 4 days on, 4 days off. 7am - 7pm. Contract : until end of December SRG are currently working with a global pharmaceutical manufacturer based in Liverpool, looking for QC Analyst - AMB (Analytical, Molecular and Bioassay) to join the team. The site in Speke specialises in the production of sterile injectable products, for the treatment of the flu. The successful individual will support the development & release of the latest Vaccine technologies, using a number of both chemical & biological testing methods. Key responsibilities: Perform analytical, biosafety & cell science testing on raw materials, intermediates and finished products Complete laboratory documentation accurately and in accordance with industry regulatory standards Utilise technical expertise to troubleshoot various assays as required Key requirements: Degree qualified in Chemistry, Biochemistry, Biomedical Science or a related scientific discipline Demonstrated practical experience a Prior industrial experience in a GMP regulated environment is highly desirable Strong verbal & written communication skills. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
Overview Replimune's mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because patient's lives depend on it. We imagine a world where cancer is a curable disease. At Replimune, we live by our values: United: We Collaborate for a Common Goal. Audacious: We Are Bold and Innovative. Dedicated: We Give Our Full Commitment. Candid: We Are Honest With Each Other . People are at the center of everything we do, and when it comes to our employees, we make it personal . With a deep sense of purpose, an innovative and collaborative culture, a competitive and forward-looking total rewards program, everyone at Replimune has a unique opportunity tocontribute to the meaningful work we do which could impact the lives of patients. Join us, as we reshape the future. Job Summary: The Associate Director, Planning and Technical Delivery, is responsible for leading the Milton Park Site planning process, coordinating stakeholders to schedule and deliver the QC batch release, stability testing and supporting studies required to meet the site objectives. Reporting to the Milton Park Site Head, the role incorporates coordination and a direct contribution within the cGMP system for monitoring, reporting, issue escalation and resolution related to direct testing and associated supporting projects. Focusing strongly on delivery, the role will drive the local tiered meeting / operating system and associated reporting / escalation. Working closely with Quality Assurance, Supply Chain and the Portfolio Strategy Team, the Associate Director Planning and Technical Delivery will represent Milton Park on cross-site project teams, coordinating local activities for future business projects as we further enhance the operating systems and capabilities of the business. This position will be located onsite in Milton Park, UK and require essential full-time attendance on site. Flexibility to travel for business is required. This position is based in our Milton Park location and typically has a 5-day on-site expectation. Responsibilities Key responsibilities: Administration of the Milton Park Site process and tools for planning, scheduling and reporting for all QC testing and batch release activities Assisting with the processing, tracking, and trending of testing activities, ensuring coordinated communications with associated stakeholders Lead the Milton Park tiered meeting operating system ensuring escalations, metrics and feedback are provided to business leads and associated stakeholders Support and/or lead deployment of new equipment, working systems or technology as part of continuous improvement to existing systems or build out of future capabilities Prepare project proposals, associated charters, project plans, benefit analysis and CAPEX proposals for approval. Drive live projects providing administrative support along with routine periodic progress reports Directly contribute to the Technical GMP project delivery, raising CCR's, authoring or approving associated reports and GMP documentation. As required, provide support to Quality Management Systems related activities (audits, investigations, deviations, CAPAs, etc.). Other responsibilities General support of all operations activities as needed. Qualifications Educational requirements: A or B.Sc. degree in a relevant biological science and extended relevant commercial experience. Experience and skill requirement: Minimum 8 years' experience in a cGMP Quality environment and 2-4 years in a managerial role; or equivalent combination of education and experience. Practical experience of QC testing in support of cGMP operations for clinical or commercial manufacturing (ATMP preferred). Excellent documentation and communication skills with a high attention to detail, enabling an effective interface with management and across the site with project teams and analysts. Experienced in project delivery within a GMP environment. Ability to work effectively in a fast-paced, regulated environment and manage multiple priorities. Must possess excellent knowledge of standard Microsoft Office programs such as Smartsheets.
Jul 22, 2025
Full time
Overview Replimune's mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because patient's lives depend on it. We imagine a world where cancer is a curable disease. At Replimune, we live by our values: United: We Collaborate for a Common Goal. Audacious: We Are Bold and Innovative. Dedicated: We Give Our Full Commitment. Candid: We Are Honest With Each Other . People are at the center of everything we do, and when it comes to our employees, we make it personal . With a deep sense of purpose, an innovative and collaborative culture, a competitive and forward-looking total rewards program, everyone at Replimune has a unique opportunity tocontribute to the meaningful work we do which could impact the lives of patients. Join us, as we reshape the future. Job Summary: The Associate Director, Planning and Technical Delivery, is responsible for leading the Milton Park Site planning process, coordinating stakeholders to schedule and deliver the QC batch release, stability testing and supporting studies required to meet the site objectives. Reporting to the Milton Park Site Head, the role incorporates coordination and a direct contribution within the cGMP system for monitoring, reporting, issue escalation and resolution related to direct testing and associated supporting projects. Focusing strongly on delivery, the role will drive the local tiered meeting / operating system and associated reporting / escalation. Working closely with Quality Assurance, Supply Chain and the Portfolio Strategy Team, the Associate Director Planning and Technical Delivery will represent Milton Park on cross-site project teams, coordinating local activities for future business projects as we further enhance the operating systems and capabilities of the business. This position will be located onsite in Milton Park, UK and require essential full-time attendance on site. Flexibility to travel for business is required. This position is based in our Milton Park location and typically has a 5-day on-site expectation. Responsibilities Key responsibilities: Administration of the Milton Park Site process and tools for planning, scheduling and reporting for all QC testing and batch release activities Assisting with the processing, tracking, and trending of testing activities, ensuring coordinated communications with associated stakeholders Lead the Milton Park tiered meeting operating system ensuring escalations, metrics and feedback are provided to business leads and associated stakeholders Support and/or lead deployment of new equipment, working systems or technology as part of continuous improvement to existing systems or build out of future capabilities Prepare project proposals, associated charters, project plans, benefit analysis and CAPEX proposals for approval. Drive live projects providing administrative support along with routine periodic progress reports Directly contribute to the Technical GMP project delivery, raising CCR's, authoring or approving associated reports and GMP documentation. As required, provide support to Quality Management Systems related activities (audits, investigations, deviations, CAPAs, etc.). Other responsibilities General support of all operations activities as needed. Qualifications Educational requirements: A or B.Sc. degree in a relevant biological science and extended relevant commercial experience. Experience and skill requirement: Minimum 8 years' experience in a cGMP Quality environment and 2-4 years in a managerial role; or equivalent combination of education and experience. Practical experience of QC testing in support of cGMP operations for clinical or commercial manufacturing (ATMP preferred). Excellent documentation and communication skills with a high attention to detail, enabling an effective interface with management and across the site with project teams and analysts. Experienced in project delivery within a GMP environment. Ability to work effectively in a fast-paced, regulated environment and manage multiple priorities. Must possess excellent knowledge of standard Microsoft Office programs such as Smartsheets.
QC Section Leader Competitive Salary + Benefits Wrexham Days Only gap technical are proud to be representing this global manufacturing business in their search for a QC Section Leader to work at their facility based near Wrexham Performance Objectives To manage the analytical testing of solid dose products. To ensure that all testing is carried out within the requirements of cGMP, Health and Safety and COSHH. To critically review analytical data, and where specifications are met, approve products for further processing. In this role, you will be responsible for leading a team of analyst and ensuring that release of our product meet the highest standards of quality and consistency. You will be a key player in driving continuous improvement and ensuring compliance with industry regulation and company polices. Person Specification Science degree in Chemistry or equivalent qualification. Previous experience within a pharmaceutical or equivalent laboratory environment is essential. A thorough understanding of current GMP, Health and Safety and COSHH regulation and sound supervisory and interpersonal skills. Manage the workload of the QC solid dose team, including preparing weekly and daily work schedules. Previous experience in leading OOS/OOT investigations and deviations is essential. Previous experience in leading a team is preferred. Previous experience in representing the QC group at internal, customer and regulatory audits and liaising with the regulatory affair department is essential Experience in leading the analytical method transfer, verification and validation is preferred Apply Please send your CV via the Apply now option on the website If you have any questions or are interested in any other opportunities we may have, please do not hesitate to get in touch This vacancy is being advertised on behalf of gap technical who are operating as an employment agency. gap technical are committed to the selection, recruitment and development of the best people, basing judgements solely on suitability for the job. Closing Date: 16/08/2025 "By applying for the above position and providing your personal data to us you understand that your data will be processed in line with our Privacy Policy."
Jul 17, 2025
Full time
QC Section Leader Competitive Salary + Benefits Wrexham Days Only gap technical are proud to be representing this global manufacturing business in their search for a QC Section Leader to work at their facility based near Wrexham Performance Objectives To manage the analytical testing of solid dose products. To ensure that all testing is carried out within the requirements of cGMP, Health and Safety and COSHH. To critically review analytical data, and where specifications are met, approve products for further processing. In this role, you will be responsible for leading a team of analyst and ensuring that release of our product meet the highest standards of quality and consistency. You will be a key player in driving continuous improvement and ensuring compliance with industry regulation and company polices. Person Specification Science degree in Chemistry or equivalent qualification. Previous experience within a pharmaceutical or equivalent laboratory environment is essential. A thorough understanding of current GMP, Health and Safety and COSHH regulation and sound supervisory and interpersonal skills. Manage the workload of the QC solid dose team, including preparing weekly and daily work schedules. Previous experience in leading OOS/OOT investigations and deviations is essential. Previous experience in leading a team is preferred. Previous experience in representing the QC group at internal, customer and regulatory audits and liaising with the regulatory affair department is essential Experience in leading the analytical method transfer, verification and validation is preferred Apply Please send your CV via the Apply now option on the website If you have any questions or are interested in any other opportunities we may have, please do not hesitate to get in touch This vacancy is being advertised on behalf of gap technical who are operating as an employment agency. gap technical are committed to the selection, recruitment and development of the best people, basing judgements solely on suitability for the job. Closing Date: 16/08/2025 "By applying for the above position and providing your personal data to us you understand that your data will be processed in line with our Privacy Policy."
Job Title: QC Analyst Job Type: Contract to End of the Year Employment Start Date: ASAP Hours of work: Mon - Fri Onsite requirement: Fully onsite Industry: Quality Location: Worthing, England Salary: 15.64 per hour - PAYE QC Analyst - Temporary We are currently recruiting QC Analysts to join our Quality Control team at the Worthing Manufacturing site. The role(s) carry out physical and chemical analytical test methods on oral products for release to market and stability studies on those products using SOPs, and accurately documenting the results as part of the Quality Control process to ensure a batch of product is of satisfactory quality. Key Responsibilities include: To test routine production and stability samples supplied from the site Value Streams and meet testing lead-time targets. Calibrate and maintain analytical equipment. Carry out qualitative and quantitative analysis of antibiotic powders and solid dose forms using a wide range of analytical techniques (eg: HPLC, Karl Fischer, dissolutions etc). To carry out OOS investigations and discuss the outcome with Team Leader, or relevant production Dept, QA manager or a Qualified Person, as required. To check and verify analytical testing and data generated by other analysts To adhere to and help maintain the highest levels of safety and GLP within the section and ensure training records are kept up to date. Daily liaison with both other analysts and team leader regarding testing and test results. May be required to take a lead role within a small team of analysts working together on a common analytical technique e.g. HPLC. Supplying data / reports to Value Stream as requested. May be required to communicate with the relevant Value Steam. to progress OOS investigations About You: This role would suit a motivated individual who has experience of working in a laboratory environment, as well as suitable qualifications in Chemistry (or scientific discipline). You will be a self-starter with keen attention to detail and compliance at the forefront of your decision-making process. A strong Quality and continuous improvement mind-set, as well as strong communication skills are also needed. About Worthing Manufacturing Site: Manufacturing at the Worthing site is for antibiotics. It is advised that you take this into consideration when deciding to apply for this position. You must disclose if you have a pre-existing penicillin allergy. When applying for this role, please use your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you provide in your CV will be used to assess your application. Basic Qualifications: Relevant scientific qualification (eg; HNC or equivalent level in scientific discipline) Understanding of laboratory analysis Relevant Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
Mar 08, 2025
Contractor
Job Title: QC Analyst Job Type: Contract to End of the Year Employment Start Date: ASAP Hours of work: Mon - Fri Onsite requirement: Fully onsite Industry: Quality Location: Worthing, England Salary: 15.64 per hour - PAYE QC Analyst - Temporary We are currently recruiting QC Analysts to join our Quality Control team at the Worthing Manufacturing site. The role(s) carry out physical and chemical analytical test methods on oral products for release to market and stability studies on those products using SOPs, and accurately documenting the results as part of the Quality Control process to ensure a batch of product is of satisfactory quality. Key Responsibilities include: To test routine production and stability samples supplied from the site Value Streams and meet testing lead-time targets. Calibrate and maintain analytical equipment. Carry out qualitative and quantitative analysis of antibiotic powders and solid dose forms using a wide range of analytical techniques (eg: HPLC, Karl Fischer, dissolutions etc). To carry out OOS investigations and discuss the outcome with Team Leader, or relevant production Dept, QA manager or a Qualified Person, as required. To check and verify analytical testing and data generated by other analysts To adhere to and help maintain the highest levels of safety and GLP within the section and ensure training records are kept up to date. Daily liaison with both other analysts and team leader regarding testing and test results. May be required to take a lead role within a small team of analysts working together on a common analytical technique e.g. HPLC. Supplying data / reports to Value Stream as requested. May be required to communicate with the relevant Value Steam. to progress OOS investigations About You: This role would suit a motivated individual who has experience of working in a laboratory environment, as well as suitable qualifications in Chemistry (or scientific discipline). You will be a self-starter with keen attention to detail and compliance at the forefront of your decision-making process. A strong Quality and continuous improvement mind-set, as well as strong communication skills are also needed. About Worthing Manufacturing Site: Manufacturing at the Worthing site is for antibiotics. It is advised that you take this into consideration when deciding to apply for this position. You must disclose if you have a pre-existing penicillin allergy. When applying for this role, please use your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you provide in your CV will be used to assess your application. Basic Qualifications: Relevant scientific qualification (eg; HNC or equivalent level in scientific discipline) Understanding of laboratory analysis Relevant Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
CK Group are recruiting for a QC Analyst, to join a company in the pharmaceutical industry, at their site based in Worthing, on a contract basis, initially until the end of the year. Salary: £15.64 per hour PAYE. QC Analyst Role: To test routine production and stability samples supplied from the site Value Streams and meet testing lead-time targets. Calibrate and maintain analytical equipment. Carry out qualitative and quantitative analysis of antibiotic powders and solid dose forms using a wide range of analytical techniques (eg: HPLC, Karl Fischer, dissolutions etc). Carry out OOS investigations and discuss the outcome with Team Leader, or relevant production Dept, QA manager or a Qualified Person, as required. Adhere to and help maintain the highest levels of safety and GLP within the section and ensure training records are kept up to date. Daily liaison with both other analysts and team leader regarding testing and test results. May be required to communicate with the relevant Value Steam. to progress OOS investigations Your Background : A bachelors degree in a relevant field or equivalent work experience. Previous experience working in a Quality Control role in the pharmaceutical industry would be preferable. GMP and/or GLP experience. Company: Our client is one of the largest global healthcare companies researching, developing and supplying innovative medicines, vaccines and healthcare products with their global headquarters in the UK. They invest around £1bn in research and development in the UK annually. Location: This role is based at our clients site in Worthing. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check. If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
Mar 06, 2025
Full time
CK Group are recruiting for a QC Analyst, to join a company in the pharmaceutical industry, at their site based in Worthing, on a contract basis, initially until the end of the year. Salary: £15.64 per hour PAYE. QC Analyst Role: To test routine production and stability samples supplied from the site Value Streams and meet testing lead-time targets. Calibrate and maintain analytical equipment. Carry out qualitative and quantitative analysis of antibiotic powders and solid dose forms using a wide range of analytical techniques (eg: HPLC, Karl Fischer, dissolutions etc). Carry out OOS investigations and discuss the outcome with Team Leader, or relevant production Dept, QA manager or a Qualified Person, as required. Adhere to and help maintain the highest levels of safety and GLP within the section and ensure training records are kept up to date. Daily liaison with both other analysts and team leader regarding testing and test results. May be required to communicate with the relevant Value Steam. to progress OOS investigations Your Background : A bachelors degree in a relevant field or equivalent work experience. Previous experience working in a Quality Control role in the pharmaceutical industry would be preferable. GMP and/or GLP experience. Company: Our client is one of the largest global healthcare companies researching, developing and supplying innovative medicines, vaccines and healthcare products with their global headquarters in the UK. They invest around £1bn in research and development in the UK annually. Location: This role is based at our clients site in Worthing. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check. If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
Per uno dei nostri Stabilimenti produttivi situato a Paderno, dedicato alla produzione di Principi Attivi e Prodotti Farmaceutici, cerchiamo un analistachimico con una esperienza pregressa, maturata in aziende con produzioni similari. Mansioni Eseguire test chimici e chimico fisici su materie prime, principi attivi, bulk e controlli in-process; Eseguire analisi su acque; Utilizzare la strumentazione di laboratorio (HPLC, GC, UV-VIS, IR, polarimetro ecc); Compilare correttamente la documentazione di laboratorio; Lavorare nel rispetto delle GMPs e delle procedure aziendali; Partecipare alla gestione della strumentazione di laboratorio. Si richiede disponibilità a turni. Diploma/Laurea in discipline scientifiche Buona conoscenza delle GMPs Conoscenza di base della lingua inglese Si richiede precedente esperienza di lavoro presso laboratorio analogo di azienda farmaceutica. La ricerca è rivolta a candidature di entrambi i sessi (L. 903/77).
Feb 20, 2025
Full time
Per uno dei nostri Stabilimenti produttivi situato a Paderno, dedicato alla produzione di Principi Attivi e Prodotti Farmaceutici, cerchiamo un analistachimico con una esperienza pregressa, maturata in aziende con produzioni similari. Mansioni Eseguire test chimici e chimico fisici su materie prime, principi attivi, bulk e controlli in-process; Eseguire analisi su acque; Utilizzare la strumentazione di laboratorio (HPLC, GC, UV-VIS, IR, polarimetro ecc); Compilare correttamente la documentazione di laboratorio; Lavorare nel rispetto delle GMPs e delle procedure aziendali; Partecipare alla gestione della strumentazione di laboratorio. Si richiede disponibilità a turni. Diploma/Laurea in discipline scientifiche Buona conoscenza delle GMPs Conoscenza di base della lingua inglese Si richiede precedente esperienza di lavoro presso laboratorio analogo di azienda farmaceutica. La ricerca è rivolta a candidature di entrambi i sessi (L. 903/77).
Main area: Behavioural and Sensory Analyst KMAH/CREST Grade NHS AfC: Band 7 Contract: Permanent Full time Flexible working 37.5 hours per week Job ref: 395-KM056-25 Site: Kent and Medway Adolescent Hospital Town: Staplehurst Salary: £46,148 - £52,809 PA Salary period: Yearly Closing: 26/02/:59 Joining means you'll become part of a welcoming and supportive working environment. We're CQC rated Good, and we want you to join us on the journey towards an Outstanding rating. NELFT has sites across North East London, Essex, Kent and Medway. We provide community and mental healthcare services to adults and children within these areas. The Trust has award-winning equality and diversity initiatives and staff health and wellbeing activities. We invest heavily in your development because when you are valued and supported, we provide the best care to our patients. We are a Level 3 Disability Confident Leader, have been featured in the Working Families Top 10 Employers benchmark for three consecutive years, and we have achieved a Carers UK Level 1 Accreditation. Along with our staff networks and training opportunities, we work hard to embed a just and compassionate culture here at NELFT. Job overview Join our Multi Disciplinary Teams as a Behavioural Analyst & Sensory Practitioner! Are you passionate about making a real difference in the lives of young people in Kent and Medway, facing complex mental health and eating disorder challenges? We are looking for a dedicated Behavioural Analyst & Sensory Practitioner to join our dynamic teams, a 14-bed adolescent inpatient unit and an Intensive Home Treatment team. This is a unique opportunity to work in a specialist setting and in the community that supports young people with a range of mental health conditions, including those requiring Naso-gastric feeding. You will be part of a multi-disciplinary team and play a vital role in developing tailored behavioural and sensory strategies, helping young people regulate emotions, build coping skills, and engage in their recovery journey. If you are ready for a rewarding, challenging, and impactful role within a compassionate, multidisciplinary team, we would love to hear from you! Main duties of the job The post-holder will provide clinical expertise and specialist behavioral and sensory assessment and treatment within their professional sphere of expertise in the service. They will be responsible for assessment, formulation and treatment, systematic outcome evaluation, and clinical supervision of junior clinicians throughout the team. The post holder will offer consultations, assessment, and treatment across KMAH & IHT services. The postholder will be accountable for their own professional actions and will work within professional ethics & Trust policies as a specialist. They will ensure that a high quality, timely, accessible, and evidence-based service is available to all service users who need it throughout the service. The post-holder will establish and maintain excellent working relationships with wider mental health and wellbeing services and ensure adherence to evidence-based treatments by all clinical staff across the team. The post-holder will be directly involved in delivering a range of therapeutic interventions, which may include parental work, group work, short-term input, and specialist psychological behavioral and/or sensory assessments and treatments. They will be responsible for working with the KMAH & IHT MDTs and providing specialist behavioral and sensory assessments and treatments within their professional sphere of expertise. Working for our organisation Probationary Period This post will be subject to a probationary period. Internal applicants are exempt from the probationary period (unless you are an internal applicant currently partway through a probationary period or currently a bank member of staff). Starting with NELFT NELFT places a great deal of importance on new starters being properly welcomed and inducted into the Trust. All new starters will join the Trust on the first Monday of each month and will undertake a comprehensive induction of up to two weeks which will include mandatory training, systems training, and the allocation of equipment. As part of the process, new starters will have the opportunity to also meet the executive team, senior managers, and attend a number of drop-in sessions focusing on engagement, health and wellbeing, and key processes. The induction will be held at our head office in Rainham, Essex. Detailed job description and main responsibilities The post holder should have relevant clinical skills and experience outlined in the job description and relevant to the role. The key responsibilities are outlined within the job description attached. The post holder will have relevant clinical, administration, communication, and training skills to be eligible for the post. The post holder will be responsible to the operation team leads, as well as the clinical lead for oversight. Person specification Qualification Relevant qualification Experience Experience (years) Experience working with children and young people Experience in robust assessments and formulation Knowledge Knowledge of working with children and young people NHS priorities and legislation Skills in the use of complex methods of behavioral assessment, intervention, and management frequently requiring sustained and intense concentration. Well-developed skills in the ability to communicate effectively, orally and in writing, complex, highly technical and/or clinically sensitive information to clients, their families, and other professional colleagues both within and outside the NHS. Skills in providing consultation to other professional and non-professional groups. We believe in bringing your authentic and best self to work, in order to deliver the best care to our patients. We are committed to supporting our employees holistically. Here is a snapshot of what is on offer at NELFT: A long-standing and award-winning approach to equality and diversity with supportive networks for ethnic minority staff, staff with disabilities or long-term/chronic conditions, and LGBT staff. A commitment to supporting colleagues to achieve a work-life balance, through flexible working opportunities and our efforts to support our working parents and carers. This has resulted in us being recognized as a 'Top 10 Family Friendly Employer' from the Working Families Charity. Proactive health and wellbeing support, including access to our employee assistance programme, staff psychological support, individual wellbeing conversations, and a network of health and wellbeing ambassadors. As a flexible working friendly organization, we want to be sure that you can work in a way that is best for us and for our patients, and for you. Speak to us about how we might be able to accommodate a flexible working arrangement whether that's a job share, part-time hours, or another flexible pattern. We recognize the valuable contribution that the Armed Forces community makes to our organization. We have signed the Armed Forces Covenant and achieved Gold Award under the Armed Forces Employer Recognition Scheme. We have supportive policies, guaranteed interview schemes for veterans, reservists, and military spouses and give additional leave to our Reservists so that they can attend their annual camp. Equal opportunities employer We are committed to equal opportunities and diversity and positively encourage applications from all sections of the community regardless of any protected characteristic. We are a Disability Confident employer and have made the pledge to commit to employing more people with disabilities. If you require this application in another format i.e. Braille or audio tape please contact the recruitment team on or email . Correspondence with us You are advised to regularly check your emails (including any junk mail/spam folders) for correspondence related to this post. As part of our recruitment process, we may be required to share information you provide on the application form with NHS Counter Fraud Authority (NHSCFA) and/or other organizations for the purpose of the prevention, detection, investigation, and prosecution of fraud or any other unlawful activity affecting the NHS. We also use third-party providers to check and verify your qualifications who may be contacting you on our behalf to verify the same. Employer certification / accreditation badges You must have appropriate UK professional registration. This post is subject to the Rehabilitation of Offenders Act 1974 (Exceptions) Order 1975 (Amendment) (England and Wales) Order 2020 and it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service.
Feb 19, 2025
Full time
Main area: Behavioural and Sensory Analyst KMAH/CREST Grade NHS AfC: Band 7 Contract: Permanent Full time Flexible working 37.5 hours per week Job ref: 395-KM056-25 Site: Kent and Medway Adolescent Hospital Town: Staplehurst Salary: £46,148 - £52,809 PA Salary period: Yearly Closing: 26/02/:59 Joining means you'll become part of a welcoming and supportive working environment. We're CQC rated Good, and we want you to join us on the journey towards an Outstanding rating. NELFT has sites across North East London, Essex, Kent and Medway. We provide community and mental healthcare services to adults and children within these areas. The Trust has award-winning equality and diversity initiatives and staff health and wellbeing activities. We invest heavily in your development because when you are valued and supported, we provide the best care to our patients. We are a Level 3 Disability Confident Leader, have been featured in the Working Families Top 10 Employers benchmark for three consecutive years, and we have achieved a Carers UK Level 1 Accreditation. Along with our staff networks and training opportunities, we work hard to embed a just and compassionate culture here at NELFT. Job overview Join our Multi Disciplinary Teams as a Behavioural Analyst & Sensory Practitioner! Are you passionate about making a real difference in the lives of young people in Kent and Medway, facing complex mental health and eating disorder challenges? We are looking for a dedicated Behavioural Analyst & Sensory Practitioner to join our dynamic teams, a 14-bed adolescent inpatient unit and an Intensive Home Treatment team. This is a unique opportunity to work in a specialist setting and in the community that supports young people with a range of mental health conditions, including those requiring Naso-gastric feeding. You will be part of a multi-disciplinary team and play a vital role in developing tailored behavioural and sensory strategies, helping young people regulate emotions, build coping skills, and engage in their recovery journey. If you are ready for a rewarding, challenging, and impactful role within a compassionate, multidisciplinary team, we would love to hear from you! Main duties of the job The post-holder will provide clinical expertise and specialist behavioral and sensory assessment and treatment within their professional sphere of expertise in the service. They will be responsible for assessment, formulation and treatment, systematic outcome evaluation, and clinical supervision of junior clinicians throughout the team. The post holder will offer consultations, assessment, and treatment across KMAH & IHT services. The postholder will be accountable for their own professional actions and will work within professional ethics & Trust policies as a specialist. They will ensure that a high quality, timely, accessible, and evidence-based service is available to all service users who need it throughout the service. The post-holder will establish and maintain excellent working relationships with wider mental health and wellbeing services and ensure adherence to evidence-based treatments by all clinical staff across the team. The post-holder will be directly involved in delivering a range of therapeutic interventions, which may include parental work, group work, short-term input, and specialist psychological behavioral and/or sensory assessments and treatments. They will be responsible for working with the KMAH & IHT MDTs and providing specialist behavioral and sensory assessments and treatments within their professional sphere of expertise. Working for our organisation Probationary Period This post will be subject to a probationary period. Internal applicants are exempt from the probationary period (unless you are an internal applicant currently partway through a probationary period or currently a bank member of staff). Starting with NELFT NELFT places a great deal of importance on new starters being properly welcomed and inducted into the Trust. All new starters will join the Trust on the first Monday of each month and will undertake a comprehensive induction of up to two weeks which will include mandatory training, systems training, and the allocation of equipment. As part of the process, new starters will have the opportunity to also meet the executive team, senior managers, and attend a number of drop-in sessions focusing on engagement, health and wellbeing, and key processes. The induction will be held at our head office in Rainham, Essex. Detailed job description and main responsibilities The post holder should have relevant clinical skills and experience outlined in the job description and relevant to the role. The key responsibilities are outlined within the job description attached. The post holder will have relevant clinical, administration, communication, and training skills to be eligible for the post. The post holder will be responsible to the operation team leads, as well as the clinical lead for oversight. Person specification Qualification Relevant qualification Experience Experience (years) Experience working with children and young people Experience in robust assessments and formulation Knowledge Knowledge of working with children and young people NHS priorities and legislation Skills in the use of complex methods of behavioral assessment, intervention, and management frequently requiring sustained and intense concentration. Well-developed skills in the ability to communicate effectively, orally and in writing, complex, highly technical and/or clinically sensitive information to clients, their families, and other professional colleagues both within and outside the NHS. Skills in providing consultation to other professional and non-professional groups. We believe in bringing your authentic and best self to work, in order to deliver the best care to our patients. We are committed to supporting our employees holistically. Here is a snapshot of what is on offer at NELFT: A long-standing and award-winning approach to equality and diversity with supportive networks for ethnic minority staff, staff with disabilities or long-term/chronic conditions, and LGBT staff. A commitment to supporting colleagues to achieve a work-life balance, through flexible working opportunities and our efforts to support our working parents and carers. This has resulted in us being recognized as a 'Top 10 Family Friendly Employer' from the Working Families Charity. Proactive health and wellbeing support, including access to our employee assistance programme, staff psychological support, individual wellbeing conversations, and a network of health and wellbeing ambassadors. As a flexible working friendly organization, we want to be sure that you can work in a way that is best for us and for our patients, and for you. Speak to us about how we might be able to accommodate a flexible working arrangement whether that's a job share, part-time hours, or another flexible pattern. We recognize the valuable contribution that the Armed Forces community makes to our organization. We have signed the Armed Forces Covenant and achieved Gold Award under the Armed Forces Employer Recognition Scheme. We have supportive policies, guaranteed interview schemes for veterans, reservists, and military spouses and give additional leave to our Reservists so that they can attend their annual camp. Equal opportunities employer We are committed to equal opportunities and diversity and positively encourage applications from all sections of the community regardless of any protected characteristic. We are a Disability Confident employer and have made the pledge to commit to employing more people with disabilities. If you require this application in another format i.e. Braille or audio tape please contact the recruitment team on or email . Correspondence with us You are advised to regularly check your emails (including any junk mail/spam folders) for correspondence related to this post. As part of our recruitment process, we may be required to share information you provide on the application form with NHS Counter Fraud Authority (NHSCFA) and/or other organizations for the purpose of the prevention, detection, investigation, and prosecution of fraud or any other unlawful activity affecting the NHS. We also use third-party providers to check and verify your qualifications who may be contacting you on our behalf to verify the same. Employer certification / accreditation badges You must have appropriate UK professional registration. This post is subject to the Rehabilitation of Offenders Act 1974 (Exceptions) Order 1975 (Amendment) (England and Wales) Order 2020 and it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service.
Global Dimensions is a HUBZone, service-disabled, veteran-owned small business based in Fredericksburg, VA. We are a dynamic, expanding company with exciting opportunities in language/culture, training/education/instruction, IT, cyber security, and intelligence (analysts, CI, HUMINT, SIGINT, etc.). Global Dimensions is currently seeking Chinese-Mandarin OLAs (Level 3) for positions in Molesworth, UK. Minimum Requirements: Must have a current TS/SCI Clearance 10 years full-time experience or 14 without degree Bachelor's degree or 4 additional years of work experience. ILR Skill Level 3 in Audio or Graphic. 10 years in crypto language processing, related language, and/or crypto experience Related Language Experience: (In target language) oral translations, non-crypto audio/graphic translations, doc exploitation, formal teaching Crypto Experience: target development, network analysis, drafting intel reports, speaker/language identification 6 of 10 years in crypto language processing - above (OLA 2) plus QC'ing, and mentoring 6 of 10 years has to be in the required language(s) 4 of 6 years performing crypto language processing 3 of 6 years simply translating, transcribing, and gisting 1 year experience QC'ing at ILR level 3 in target language No more than 3 of 10 years reporting as primary duty 1 of 6 years in target language has to be within 6 years of resume submission. Global Dimensions does not discriminate on the basis of race, sex, color, religion, age, national origin, marital status, disability, veteran status, genetic information, sexual orientation, gender identity or any other reason prohibited by law in provision of employment opportunities and benefits. Equal Opportunity Employer/Veterans/Disabled.
Feb 17, 2025
Full time
Global Dimensions is a HUBZone, service-disabled, veteran-owned small business based in Fredericksburg, VA. We are a dynamic, expanding company with exciting opportunities in language/culture, training/education/instruction, IT, cyber security, and intelligence (analysts, CI, HUMINT, SIGINT, etc.). Global Dimensions is currently seeking Chinese-Mandarin OLAs (Level 3) for positions in Molesworth, UK. Minimum Requirements: Must have a current TS/SCI Clearance 10 years full-time experience or 14 without degree Bachelor's degree or 4 additional years of work experience. ILR Skill Level 3 in Audio or Graphic. 10 years in crypto language processing, related language, and/or crypto experience Related Language Experience: (In target language) oral translations, non-crypto audio/graphic translations, doc exploitation, formal teaching Crypto Experience: target development, network analysis, drafting intel reports, speaker/language identification 6 of 10 years in crypto language processing - above (OLA 2) plus QC'ing, and mentoring 6 of 10 years has to be in the required language(s) 4 of 6 years performing crypto language processing 3 of 6 years simply translating, transcribing, and gisting 1 year experience QC'ing at ILR level 3 in target language No more than 3 of 10 years reporting as primary duty 1 of 6 years in target language has to be within 6 years of resume submission. Global Dimensions does not discriminate on the basis of race, sex, color, religion, age, national origin, marital status, disability, veteran status, genetic information, sexual orientation, gender identity or any other reason prohibited by law in provision of employment opportunities and benefits. Equal Opportunity Employer/Veterans/Disabled.
Associate Vice President, Service Desk Manager Apply locations London, UK time type Full time posted on Posted 8 Days Ago job requisition id R5879 Over the last 20 years, Ares' success has been driven by our people and our culture. Today, our team is guided by our core values - Collaborative, Responsible, Entrepreneurial, Self-Aware, Trustworthy - and our purpose to be a catalyst for shared prosperity and a better future. Through our recruitment, career development and employee-focused programming, we are committed to fostering a welcoming and inclusive work environment where high-performance talent of diverse backgrounds, experiences, and perspectives can build careers within this exciting and growing industry. Job Description Summary: Ares Management is currently seeking a Service Desk Manager to join the End User Support team within the Technology & Information Security organization. The IT team consists of over 200 team members globally and is responsible for the firm's technology landscape. The Service Desk team within IT supports all Ares employees, including those in other locations, remotely as needed. The group is responsible for providing excellent client service while serving as points of contact for end users in troubleshooting requests, promptly responding to questions, and resolving Technology-related issues. They are also responsible for aligning themselves with the relevant business units and departments and proactively strategizing business needs as it pertains to Technology requirements. Service Desk management is responsible for overseeing the Service Desk support team in their respective locations (London and all other locations within EMEA) by supporting them in their daily tasks of responding to and resolving incidents and/or request tickets. The primary focus of this role is to monitor productivity, manage projects, delegate tasks, provide guidance, handle escalations and create a work environment that is professional, collaborative and enjoyable so service level goals can be achieved. Though the primary responsibility is management, there will be occasions where some hands-on technical work is required. Primary Functions & Essential Responsibilities: Day to day management of Service Desk Analysts, Senior Analysts, consultants Oversee the daily operation of Service Desk functions that include first level phone, email and walk-in support, logging of incidents and requests in the service management system, etc. Ensure the highest level of service delivery for all clients within the firm Accountable for providing leadership, direction, career path opportunities, mentorship and coaching to Service Desk team Ensure that individual and team responsibilities are performed in a timely, consistent, and responsive manner Verify the quality, accuracy and timeliness of responses and actions taken by the Service Desk team Engage business stakeholders to ensure service levels exceed expectations Partner with colleagues to develop metrics / OLA's / KPI's to drive operational efficiencies Prioritize workloads and balance conflicting demands, provide delegation on tasks and manage escalations as appropriate Provide guidance and advice on specific tasks and requests Manage weekly staff meetings Provide ongoing performance feedback to team members and monitor trends in individual and team performance Identify training requirements for team and train all team members as part of the onboarding process, and all existing team members on new processes or requirements Identify issues and make recommendations that will improve processes and procedures Assist in strategic initiatives through brainstorming and implementation, etc. Manage vendor accounts and relationships Manage special projects as assigned Partner with management to help refine the overall service strategy for the firm Own the front-line support experience for the EMEA Region Education: BS/BA in Computer Science, Business Administration or equivalent experience Certifications Desired may include: HDI Certifications ITIL/ITSM Foundation Certification Six Sigma Green belt (min) Certifications Microsoft Certifications CompTia Certifications (A+/Sec+/Net+) Experience Required: Experience in the financial services sector and/or alternate asset management experience preferred A minimum of 8 years of relevant experience with at least 3 years in a leadership role Proven people leader - hiring, developing, and fostering talent; building high-performing teams; driving change across scaled and global teams Experience leading staff in a Service Desk operation Experience with ITIL based ticket tracking systems such as ServiceNow and automatic call distribution systems Demonstrates commitment to providing Quality Customer Experience (QCE) Talent for creatively utilizing technology, people and processes to solve unique business problems in a cost-effective manner. Exceptional critical thinker and strong business judgment Ability to design and document processes Intermediate Excel skills; familiarity with formulas and pivot tables Track record of strong performance General Requirements: Ability to manage challenging workflow in a fast-paced, dynamic organization, managing multiple assignments in a deadline driven environment Experience managing internal and external stakeholders and leading project prioritization discussions to drive roadmap Strong management skills, including proven experience of managing and/or collaborating with teams in remote locations to ensure efficiency, effectiveness, and high level of supervisory oversight Ability to extract meaningful information from extensive research and analysis to effectively present facts and findings in a digestible format, a keen eye for attention to detail Strong sense of ownership and accountability Organizational skills, demonstrated ability to manage competing priorities and lead large scale projects to completion Ability to multi-task and prioritize deadlines; result oriented Change agent / leader, self-motivated, self-starter High accuracy and detail orientation Excellent communication (written, verbal, presentation, documentation) and client service skills; capability of interacting with key stakeholders to direct prioritization of program related activity Experience and ability to proactively and continuously identify and analyze problem situations to develop an effective and improve course of action for resolution Ability to work independently within a fast-paced environment with a hands-on approach Ability to be flexible in terms of hours in order to coordinate with team members across time zones Comfort in dealing with ambiguity and uncertainty in a dynamic environment Dependable, great attitude, highly motivated and a team player Reporting Relationships: Vice President, Service Desk There is no set deadline to apply for this job opportunity. Applications will be accepted on an ongoing basis until the search is no longer active.
Feb 13, 2025
Full time
Associate Vice President, Service Desk Manager Apply locations London, UK time type Full time posted on Posted 8 Days Ago job requisition id R5879 Over the last 20 years, Ares' success has been driven by our people and our culture. Today, our team is guided by our core values - Collaborative, Responsible, Entrepreneurial, Self-Aware, Trustworthy - and our purpose to be a catalyst for shared prosperity and a better future. Through our recruitment, career development and employee-focused programming, we are committed to fostering a welcoming and inclusive work environment where high-performance talent of diverse backgrounds, experiences, and perspectives can build careers within this exciting and growing industry. Job Description Summary: Ares Management is currently seeking a Service Desk Manager to join the End User Support team within the Technology & Information Security organization. The IT team consists of over 200 team members globally and is responsible for the firm's technology landscape. The Service Desk team within IT supports all Ares employees, including those in other locations, remotely as needed. The group is responsible for providing excellent client service while serving as points of contact for end users in troubleshooting requests, promptly responding to questions, and resolving Technology-related issues. They are also responsible for aligning themselves with the relevant business units and departments and proactively strategizing business needs as it pertains to Technology requirements. Service Desk management is responsible for overseeing the Service Desk support team in their respective locations (London and all other locations within EMEA) by supporting them in their daily tasks of responding to and resolving incidents and/or request tickets. The primary focus of this role is to monitor productivity, manage projects, delegate tasks, provide guidance, handle escalations and create a work environment that is professional, collaborative and enjoyable so service level goals can be achieved. Though the primary responsibility is management, there will be occasions where some hands-on technical work is required. Primary Functions & Essential Responsibilities: Day to day management of Service Desk Analysts, Senior Analysts, consultants Oversee the daily operation of Service Desk functions that include first level phone, email and walk-in support, logging of incidents and requests in the service management system, etc. Ensure the highest level of service delivery for all clients within the firm Accountable for providing leadership, direction, career path opportunities, mentorship and coaching to Service Desk team Ensure that individual and team responsibilities are performed in a timely, consistent, and responsive manner Verify the quality, accuracy and timeliness of responses and actions taken by the Service Desk team Engage business stakeholders to ensure service levels exceed expectations Partner with colleagues to develop metrics / OLA's / KPI's to drive operational efficiencies Prioritize workloads and balance conflicting demands, provide delegation on tasks and manage escalations as appropriate Provide guidance and advice on specific tasks and requests Manage weekly staff meetings Provide ongoing performance feedback to team members and monitor trends in individual and team performance Identify training requirements for team and train all team members as part of the onboarding process, and all existing team members on new processes or requirements Identify issues and make recommendations that will improve processes and procedures Assist in strategic initiatives through brainstorming and implementation, etc. Manage vendor accounts and relationships Manage special projects as assigned Partner with management to help refine the overall service strategy for the firm Own the front-line support experience for the EMEA Region Education: BS/BA in Computer Science, Business Administration or equivalent experience Certifications Desired may include: HDI Certifications ITIL/ITSM Foundation Certification Six Sigma Green belt (min) Certifications Microsoft Certifications CompTia Certifications (A+/Sec+/Net+) Experience Required: Experience in the financial services sector and/or alternate asset management experience preferred A minimum of 8 years of relevant experience with at least 3 years in a leadership role Proven people leader - hiring, developing, and fostering talent; building high-performing teams; driving change across scaled and global teams Experience leading staff in a Service Desk operation Experience with ITIL based ticket tracking systems such as ServiceNow and automatic call distribution systems Demonstrates commitment to providing Quality Customer Experience (QCE) Talent for creatively utilizing technology, people and processes to solve unique business problems in a cost-effective manner. Exceptional critical thinker and strong business judgment Ability to design and document processes Intermediate Excel skills; familiarity with formulas and pivot tables Track record of strong performance General Requirements: Ability to manage challenging workflow in a fast-paced, dynamic organization, managing multiple assignments in a deadline driven environment Experience managing internal and external stakeholders and leading project prioritization discussions to drive roadmap Strong management skills, including proven experience of managing and/or collaborating with teams in remote locations to ensure efficiency, effectiveness, and high level of supervisory oversight Ability to extract meaningful information from extensive research and analysis to effectively present facts and findings in a digestible format, a keen eye for attention to detail Strong sense of ownership and accountability Organizational skills, demonstrated ability to manage competing priorities and lead large scale projects to completion Ability to multi-task and prioritize deadlines; result oriented Change agent / leader, self-motivated, self-starter High accuracy and detail orientation Excellent communication (written, verbal, presentation, documentation) and client service skills; capability of interacting with key stakeholders to direct prioritization of program related activity Experience and ability to proactively and continuously identify and analyze problem situations to develop an effective and improve course of action for resolution Ability to work independently within a fast-paced environment with a hands-on approach Ability to be flexible in terms of hours in order to coordinate with team members across time zones Comfort in dealing with ambiguity and uncertainty in a dynamic environment Dependable, great attitude, highly motivated and a team player Reporting Relationships: Vice President, Service Desk There is no set deadline to apply for this job opportunity. Applications will be accepted on an ongoing basis until the search is no longer active.
Senior QC Analyst Validation We have a brand new role to join a global quality team where you will be vital in delivering active ingredients that meet the highest pharmaceutical regulatory and compliance standards. The role will initially be for 23 months but may be extended. Responsibilities Troubleshoot analytical equipment and technique failures. Promote technical skills and quality standards within QC. Conduct sample analysis, validation activities, and batch releases. Own analytical projects and ensure compliance with GMP and QA standards. Collaborate on continuous improvement initiatives and meet corporate quality goals. About you You will have a degree in a relevant science field along with proven experience with HPLC, GC FTIR, UV, PXRD, DSC. In addition, you will have a strong understanding of GMP and analytical method validation/transfer principles. What's on offer? Competitive hourly rate and retention bonus. Professional training and development. 36-hour workweek (Monday-Friday). Opportunity to contribute to global pharmaceutical innovation. Unfortunately, we are unable to provide sponsorship for this role so please only apply if you have the right to work in the UK.
Jan 29, 2025
Full time
Senior QC Analyst Validation We have a brand new role to join a global quality team where you will be vital in delivering active ingredients that meet the highest pharmaceutical regulatory and compliance standards. The role will initially be for 23 months but may be extended. Responsibilities Troubleshoot analytical equipment and technique failures. Promote technical skills and quality standards within QC. Conduct sample analysis, validation activities, and batch releases. Own analytical projects and ensure compliance with GMP and QA standards. Collaborate on continuous improvement initiatives and meet corporate quality goals. About you You will have a degree in a relevant science field along with proven experience with HPLC, GC FTIR, UV, PXRD, DSC. In addition, you will have a strong understanding of GMP and analytical method validation/transfer principles. What's on offer? Competitive hourly rate and retention bonus. Professional training and development. 36-hour workweek (Monday-Friday). Opportunity to contribute to global pharmaceutical innovation. Unfortunately, we are unable to provide sponsorship for this role so please only apply if you have the right to work in the UK.
QC Analyst - Finished Products SRG are recruiting for a Quality Control Analyst (QC) to be based with a rapidly growing pharmaceutical producer in West Yorkshire. Manufacturing numerous household brands found in homes across the country, they also produce specialist prescription products for the NHS. This position will play an essential part in ensuring that medicines & pharmaceuticals produced onsite, are of the highest quality & safe to use. The role As a QC analyst, you will be responsible for the routine testing of samples Utilising HPLC, UV, IR & Gravimetric analysis. Key duties will include: Carry out the efficient analysis of incoming samples Ensure all activities are carried out in line with GMP & ISO quality standards. Meet testing schedules to ensure products are released in a timely manner. Keep accurate and detailed records, providing regular feedback & progress reports. Working Hours: 38 hours per week This will be a shift allowance working: 06:00 - 13:30 13:30 - 22:00 (17:00 finish on Fridays) Requirements: A degree or similar qualification or experience in a relevant subject. Experience using HPLC. Previous experience within an analytical laboratory. A keen eye for detail and record keeping. Full right to work in the UK; no sponsorship can be offered, Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
Jan 29, 2025
Seasonal
QC Analyst - Finished Products SRG are recruiting for a Quality Control Analyst (QC) to be based with a rapidly growing pharmaceutical producer in West Yorkshire. Manufacturing numerous household brands found in homes across the country, they also produce specialist prescription products for the NHS. This position will play an essential part in ensuring that medicines & pharmaceuticals produced onsite, are of the highest quality & safe to use. The role As a QC analyst, you will be responsible for the routine testing of samples Utilising HPLC, UV, IR & Gravimetric analysis. Key duties will include: Carry out the efficient analysis of incoming samples Ensure all activities are carried out in line with GMP & ISO quality standards. Meet testing schedules to ensure products are released in a timely manner. Keep accurate and detailed records, providing regular feedback & progress reports. Working Hours: 38 hours per week This will be a shift allowance working: 06:00 - 13:30 13:30 - 22:00 (17:00 finish on Fridays) Requirements: A degree or similar qualification or experience in a relevant subject. Experience using HPLC. Previous experience within an analytical laboratory. A keen eye for detail and record keeping. Full right to work in the UK; no sponsorship can be offered, Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
QC Analyst - Raw Materials SRG are recruiting for a Quality Control Analyst (QC) to be based with a rapidly growing pharmaceutical producer in West Yorkshire. Manufacturing numerous household brands found in homes across the country, they also produce specialist prescription products for the NHS. This position will play an essential part in ensuring that medicines & pharmaceuticals produced onsite, are of the highest quality & safe to use. The role As a QC analyst, you will be responsible for the routine testing of samples Utilising HPLC, UV, IR & Gravimetric analysis. Key duties will include: Carry out the efficient analysis of incoming samples Ensure all activities are carried out in line with GMP & ISO quality standards. Meet testing schedules to ensure products are released in a timely manner. Keep accurate and detailed records, providing regular feedback & progress reports. Working Hours: 38 hours per week This will be a shift allowance working: 06:00 - 13:30 13:30 - 22:00 (17:00 finish on Fridays) Requirements: A degree or similar qualification or experience in a relevant subject. Experience using HPLC. Previous experience within an analytical laboratory. A keen eye for detail and record keeping. Full right to work in the UK; no sponsorship can be offered. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
Jan 29, 2025
Full time
QC Analyst - Raw Materials SRG are recruiting for a Quality Control Analyst (QC) to be based with a rapidly growing pharmaceutical producer in West Yorkshire. Manufacturing numerous household brands found in homes across the country, they also produce specialist prescription products for the NHS. This position will play an essential part in ensuring that medicines & pharmaceuticals produced onsite, are of the highest quality & safe to use. The role As a QC analyst, you will be responsible for the routine testing of samples Utilising HPLC, UV, IR & Gravimetric analysis. Key duties will include: Carry out the efficient analysis of incoming samples Ensure all activities are carried out in line with GMP & ISO quality standards. Meet testing schedules to ensure products are released in a timely manner. Keep accurate and detailed records, providing regular feedback & progress reports. Working Hours: 38 hours per week This will be a shift allowance working: 06:00 - 13:30 13:30 - 22:00 (17:00 finish on Fridays) Requirements: A degree or similar qualification or experience in a relevant subject. Experience using HPLC. Previous experience within an analytical laboratory. A keen eye for detail and record keeping. Full right to work in the UK; no sponsorship can be offered. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
Role: QC Analyst Permanent Location: Morpeth Competitive Salary + Shift allowance An exciting opportunity has become available due to internal growth in the team. We're looking for a QC Analyst with at least one year of experience within the pharmaceutical industry. This role is working shifts and comes with a very generous shift allowance. The Role: QC Analyst Testing of a range of products using wet chemical and instrumental techniques such as TLC, HPLC, FTIR, UV analysis to agreed timescales Generating valid QC testing data in accordance with Company Policy and regulatory compliance to agreed time scales Carrying out routine equipment maintenance and calibration of laboratory equipment following approved methods and procedures on assigned pieces of equipment The successful candidate: Experience within the pharmaceutical industry Relevant Scientific Degree Experience of using techniques such as TLC, HPLC, FTIR or UV Experience writing and reviewing SOPS To apply for the Senior Quality Control Analyst or here more information, please contact Jack Challinor at Smart4Sciecnes on
Jan 29, 2025
Full time
Role: QC Analyst Permanent Location: Morpeth Competitive Salary + Shift allowance An exciting opportunity has become available due to internal growth in the team. We're looking for a QC Analyst with at least one year of experience within the pharmaceutical industry. This role is working shifts and comes with a very generous shift allowance. The Role: QC Analyst Testing of a range of products using wet chemical and instrumental techniques such as TLC, HPLC, FTIR, UV analysis to agreed timescales Generating valid QC testing data in accordance with Company Policy and regulatory compliance to agreed time scales Carrying out routine equipment maintenance and calibration of laboratory equipment following approved methods and procedures on assigned pieces of equipment The successful candidate: Experience within the pharmaceutical industry Relevant Scientific Degree Experience of using techniques such as TLC, HPLC, FTIR or UV Experience writing and reviewing SOPS To apply for the Senior Quality Control Analyst or here more information, please contact Jack Challinor at Smart4Sciecnes on