Talentmark

Talentmark are recruiting for an Account Manager, to join a pharmaceutical company, based in Birmingham, on a permanent basis. The salary is around 28,000- 34,000 per annum. The Company: Our client are a Pharmaceutical manufacturing company who produce, import, and distribute bespoke medicines. Your main duties will be: Manage the end-to-end customer journey from onboarding to retention. Act as the primary point of contact for a portfolio of clients. Liaise with customers to ensure timely and effective communication regarding orders, services and inquiries. Collaborate across departments to ensure a seamless customer experience. Maintain accurate records and provide regular reports to management. Your Background (Essential): Degree in scientific, pharmaceutical or quality-related discipline. Minimum of 3 years experience in a customer success, account management or customer-facing role. Flexibility to travel across the UK and Ireland. Your Background (Desirable): Experience in a GMP, pharmaceutical, specials or other regulated environment. Knowledge of Specials Manufacturing regulatory requirements and MHRA guidance. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference (phone number removed) in all correspondence. 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 (Talentmark) and follow us to see our latest jobs and company news.

Talentmark are recruiting for an Associate Scientist to join a company in the medical devices industry on a contract basis for 12 months. This role is fully site-based in Motherwell. Salary: From 14.30 per hour to 16.86 per hour PAYE Associate Scientist Role: Conduct and plan small-scale experiments independently. Assist in the design and development of complex experiments and multiple diagnostic assays. Analyse experimental data and deliver clear technical conclusions, summaries, and recommendations. Maintain and calibrate laboratory equipment. Proactively identify errors or out-of-trend results, suggesting inventive solutions and continuous improvements to protocols and test methods. Present summaries of work at team meetings and to cross-functional groups. Your Background: Hold a relevant degree in a scientific subject. Working knowledge of GLP/GDP standards, Design Control, Health & Safety, biosafety protocols, COSHH, and risk management compliance. You are a methodical, detail-oriented, and curious scientist who excels in laboratory execution and thrives in collaborative team settings. You have exceptional attention to detail, strong numeracy skills, and a proactive approach. Strong communication skills with a track record of effectively presenting scientific data to peers and cross-functional teams. Company: Our client is one of the world's premier innovative biopharmaceutical and medical device companies that help improve the lives of millions of people in the UK and around the world every year. Apply: For more information, or to apply for this Associate Scientist, please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only). It is essential that applicants hold entitlement to work in the UK Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

Talentmark is recruiting for a Product Definition lead to join a company in the medical devices industry on a contract basis for 12 months. This role is fully site-based in Motherwell. Salary: From 22.98 to 25.54 per hour PAYE Product Definition Lead Role: Drive the success of our product definition initiatives and guide the technical direction of complex systems. Manage, coach and develop a team of specialised systems and requirements engineers Oversee and lead the product definition for technically complex POC systems Drive requirements engineering, elicitation, and thorough evaluations for completeness Support the engineering team with technical issue identification, rapid resolution and closure. Your Background: Hold a Master's or PhD in engineering, life sciences, or a related scientific subject. A proven track record of 5 or more years in requirements engineering, systems engineering, or product definition, preferably within the medical device, diagnostics, or a heavily regulated industry. Demonstrated leadership capabilities and a true passion for solving problems both individually and in collaborative, interdisciplinary team settings. A high degree of flexibility, proactiveness, and strategic vision to steer point-of-care platforms in line with global business goals. Strong communication, problem-solving, and quick-thinking skills, with a track record of translating business and clinical needs into precise requirements. Company: Our client is one of the world's premier innovative biopharmaceutical and medical device companies that help improve the lives of millions of people in the UK and around the world every year. Apply: For more information, or to apply for this Product Definition Lead, please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only). It is essential that applicants hold entitlement to work in the UK Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

Talentmark are recruiting for an Import & Export Coordinator to join a global animal health company on a contract basis for 12 months. This role is 30 hours per week with 2 days on site in Pirbright, Surrey. Salary: Up to 19.50 per hour PAYE Import & Export Coordinator Role: Be the main site contact for import, export and compliance matters. Support the development and delivery of import/export compliance training. Work with internal teams to ensure import/export requirements are fully met. Maintain and continuously improve Standard Operating Procedures. Support logistics activities, including vehicle bookings, packing oversight and visual inspections. Your Background : Formal training in import/export or customs. Hands-on experience in broad import/export operations, preferably in the pharma or animal health industry. Knowledge of GDP, GXP, GMP, Dangerous Goods and corporate governance. Excellent stakeholder management skills. Exceptional attention to detail, communication and problem-solving skills. Company: Our client is a leading manufacturer of vaccines, parasiticides and pharmaceuticals to protect animals. They are also one of the fastest-growing animal health companies in the UK. Apply: For more information, or to apply for this Import & Export Coordinator, please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only) . It is essential that applicants hold entitlement to work in the UK Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

Talentmark are recruiting for a Real World Evidence Expert to join a global pharmaceutical company on a contract basis initially for 6-months . Salary: 40.62 to 45 phr PAYE or 55.87 to 60 phr Umbrella Real World Evidence Expert Role: Design and run global real-world evidence (RWE) studies from concept through to publication. Work on a collaborative study with an academic partner to grow a rare disease registry. Write study concepts, protocols, and statistical analysis plans. Lead secondary data studies and represent RWE on primary data collection teams. Interpret and communicate results to internal and external stakeholders. Your Background: Proven track record delivering RWE projects using primary or secondary data. Experience gained in pharma, a specialist consultancy, or an academic centre of excellence. A PhD in epidemiology or outcomes research is desirable. Experience with academic collaborations or key opinion leaders is a plus. Experience with patient or carer-provided data, ideally in rare disease, is a plus. Company: Our client is a global biopharmaceutical company focused on creating value for people living with severe diseases in immunology and neurology now and into the future. Location: This role is based at our client's site in Slough, offering Hybrid or Full remote working. Apply: For more information, or to apply for this Real World Evidence Expert role please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only) . It is essential that applicants hold entitlement to work in the UK. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

Talentmark are recruiting for a Field Applications Specialist to join a company in the pharmaceutical industry on a contract basis for 12 months. Salary: 180 to 230 per day PAYE, or 245.27 to 305.06 per day Umbrella. Field Applications Specialist Role: - Support customers using lab testing equipment. - Fix technical problems quickly and keep machines running. - Reduce equipment downtime as much as possible. - Help with software and IT issues on site. - Train lab staff on how to use the equipment. Your Background: - A biomedical science degree, or equivalent hands-on experience. - Good knowledge of the diagnostics industry. - Experience supporting a hospital lab or similar diagnostics setting. - Strong problem-solving skills. Company: Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year. Location: This is a remote role, and you'll need to live in or near Devon. You'll cover 3 hospitals in the region. Some travel is needed further afield, including occasional visits to Burgess Hill. Overnight stays away from home may be needed now and then, but not regularly. Apply: For more information, or to apply for this Field Applications Specialist role, please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only) It is essential that applicants hold entitlement to work in the UK. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check. This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

Talentmark are recruiting for a QA Officer on behalf of a growing manufacturer of Active Pharmaceutical Ingredients, to be based at their site in Kent on a permanent basis. The Role: This role offers exposure to the full Quality Assurance lifecycle and the opportunity to broaden your experience across multiple quality systems. You will be trusted to take ownership, contribute ideas and make a genuine impact within a growing business. Key Responsibilities: Maintaining and continually improving the Quality Management System (QMS). Reviewing and approving batch manufacturing documentation prior to batch release, SOPs, controlled documents and quality records. Managing Deviations, CAPAs, Change Controls, Complaints and OOS investigations and supporting product recalls and quality investigations where required Supporting internal and supplier audits and assisting with customer and regulatory audits. Supporting supplier qualification and Quality Agreements. Maintaining training records and ensuring GMP compliance throughout the business. Your Background: Educated to degree level or above in Life Sciences or a related field. Established Quality Assurance experience within a GMP pharmaceutical manufacturing environment. Experience of QMS, CAPAs, Deviations, Change Controls and batch record review. Ideally experience of internal or supplier audits, Validation and Supplier Quality. Ability to write clear technical reports and quality documentation. Excellent communication skills and confidence working across all departments Benefits Permanent full-time position Monday-Friday working 31 days holiday (including Bank Holidays) Company Pension Company Bonus Scheme Private Health Care On-site parking Access to on-site gym and Cafeteria Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference (phone number removed) in all correspondence.

Talentmark are recruiting for a Strategic Sourcing Manager to join a company in the pharmaceutical industry on a contract basis for 12-months. Salary: 263.88 to 301.57 per day PAYE or 350 to 400 per day Umbrella/Ltd. Daily duties of a Strategic Sourcing Manager: You'll lead sourcing and category activity across the clinical laboratories space, covering areas such as genomics, bioanalytics, flow cytometry and central labs. Build and execute sourcing strategies, drawing on your category know-how and negotiation skills. Manage supplier relationships and contracts, driving value and reducing risk across the supply base. Work closely with internal procurement teams and business stakeholders, turning what the business needs into practical sourcing plans. Day-to-day, you'll support core procurement operations while contributing to wider projects that improve the buying experience for everyone involved. Your Background: A university degree, ideally in business or a science-related subject such as life sciences, chemistry or biochemistry. At least 5 years of procurement experience in strategic sourcing and project delivery, with a solid grasp of contracting. Experience with procurement systems and processes. A in ideally within pharmaceutical or R&D categories, with an understanding of related regulations. Strong project management skills and fluent business-level English. Company: Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing healthcare products to help improve the lives of millions of people in the UK and around the world every year. Location: This role is based at our client's site in Welwyn on a hybrid basis, with 2 days per week in the office. Apply: Fancy finding out more, or ready to apply for this Strategic Sourcing Manager role? Contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only) . It is essential that applicants hold entitlement to work in the UK. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

Talentmark are recruiting for a QC Microbiology Technician to join a global healthcare provider to hospitals, clinics and homes on a contract basis for 11 months. This role is based at the client's site in Swindon. Salary: 13.58 per hour PAYE. Shift This role is days only, (Apply online only), but is on a rotating shift including weekends. QC Microbiology Technician Role: Test the microbiological properties of materials and products. Collect Environmental monitoring and water samples. Update the batch tracker with Microbiology testing dates. Keep environmental monitoring tracking spreadsheets up to date, including trending data and transcription checking. Provide technical support to Scientist 2 and Senior Scientist, including technician duties when required. Your Background : Hold a relevant scientific qualification or have working experience in a lab. Good knowledge of microbiology and testing techniques. Have an understanding of GMP/GLP environments. Ability to work weekends. Company: Our client is the global leader in enabling pharma, biotech, and consumer health partners to optimise product development, launch, and full life-cycle supply for patients around the world. They have the goal of putting patients first and to help people around the world live better and healthier lives. Apply: For more information, or to apply for this QC Microbiology Technician, please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only). It is essential that applicants hold entitlement to work in the UK Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

Talentmark are recruiting for a Forklift Driver to join a resin and composites company on a contract basis for 3 months initially, with the likelihood of extension. This role is fully site-based in Wrexham. Salary: 13.82 per hour PAYE Warehouse Operative Role: Receiving of raw materials. Preparing and shipping customer orders. Issuing goods to production. Locating stock and daily inventory checks. Dealing with forwarders, coordinating transport. Your Background: A Forklift licence is required for this role (in-house experience may also be considered). Experience with goods receiving, checking goods for defects. Experience in dealing with the shipping of hazardous goods and preparing regulated documents. Show strong commitment to all aspects of safety due to experience in similar environments. Have a high attention to detail and be willing to learn new skills. Company: Our client is an advanced materials and speciality chemical company focused on the manufacture of resins. Apply: For more information, or to apply for this Fork Lift Driver position, please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only). It is essential that applicants hold entitlement to work in the UK. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

QC Scientist Location: Near Peterborough, Cambridgeshire Job Type: Full-Time, Permanent Talentmark is recruiting for a QC Scientist to join a growing bioscience organisation operating within a GMP-regulated environment. This is an excellent opportunity for an analytical scientist with experience in chromatographic techniques to play a key role in quality control testing, supporting the manufacture and processing of high-quality, plant-derived active pharmaceutical ingredients (APIs). Key Responsibilities: Perform analytical testing of plant-derived molecules in accordance with approved SOPs. Prepare working solutions, mobile phases, standards, and laboratory reagents. Maintain accurate GMP-compliant documentation and ensure data integrity requirements are met. Carry out routine maintenance, calibration, and verification of laboratory instrumentation, including GC-MS and HPLC-UV systems. Manage laboratory stock levels and consumables to support uninterrupted testing activities. Support internal audits and regulatory inspections where required. Participate in data review activities and continuous improvement initiatives. Collaborate closely with QA, Production, and other cross-functional teams. Your Background: Degree-qualified in Chemistry or a related scientific discipline, or possess equivalent laboratory experience. Experience working within a regulated laboratory environment, ideally GMP. Familiarity with analytical techniques such as HPLC and/or GC-MS. Strong understanding of laboratory safety practices, including COSHH, risk assessments, and PPE requirements. What's on Offer? Opportunity to join an innovative bioscience organisation with ambitious growth plans. Collaborative and fast-paced working environment. Work within a modern GMP-regulated laboratory environment. Exposure to cutting-edge products and technologies. If you're a motivated analytical scientist looking to further your career within quality control and GMP manufacturing, we'd love to hear from you. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence.

Talentmark are recruiting for a Legal Partner to join a company in the pharmaceutical industry on a contract basis for 12 months. Salary: 450 - 580 per day PAYE or .13 per day Umbrella. Legal Partner Role: Give legal advice and support across the UK and Ireland business. Handle data protection matters, including subject access requests and privacy issues. Advise teams on clinical trials, including reviewing and negotiating agreements. Help the business stay compliant with pharmaceutical laws and codes of conduct. Spot legal risks early and help the business plan around them. Your Background: Qualified lawyer in England and Wales. Solid, practical knowledge of UK data protection law (UK GDPR). Good understanding of UK commercial pharmaceutical law. Experience working in the life sciences or pharmaceutical industry. Knowledge of medical device or digital health regulations is a bonus, not a must. Company: Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year. Location: This role is based at our client's site in Welwyn, 3 days per week in the office. Apply: For more information, or to apply for this Legal Partner role, please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only) It is essential that applicants hold entitlement to work in the UK. Please note: this role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

Talentmark are recruiting for an Associate Director, Drug Safety to join a company in the pharmaceutical industry on a contract basis for 12 months . Salary: 67.96 - 75.51 per hour PAYE or 90 - 100 per hour Umbrella/Ltd. Associate Director, Drug Safety Role: Provide safety oversight and input across the full study lifecycle, from early development through to post-market. Lead post-market safety work, including signal evaluation, benefit-risk assessment and risk management. Own case reporting, including aggregate reports such as DSUR and PBRER. Drive signal detection and contribute to the strategic review of safety reports. Prepare and maintain risk management documents, including CCDS, labelling documents, RMPs and REMS. Your Background: Strong understanding of GxP, regulated processes and the clinical trial lifecycle. Confident communicator, able to work with remote teams across different countries. Skilled in data analysis and statistical methods, with the ability to present findings clearly. Strong presenter, able to summarise key points for different audiences. Able to work independently with minimal supervision. A postgraduate qualification in a life sciences field (PhD, MSc, medical or PharmD) is preferred but not essential. Company: Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing products to help improve the lives of millions of people in the UK and around the world every year. L ocation: This role is based at our client's site in Welwyn, 2 days per week in the office. Apply For more information, or to apply for this Associate Director, Drug Safety role please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only). It is essential that applicants hold entitlement to work in the UK. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

Talentmark are recruiting for a Laboratory Technician, to join our client based in Penryn Cornwall. Our client devlelops and applies technologies to recover valuable metals from mine waste, such as tailings, slag heaps, and waste dumps. It is a fantastic opportunity for someone to build upon their chemistry skills within a laboratory based role. This is a permanent role, Monday to Friday, 9am - 5pm. Our client devlelops and applies technologies to recover valuable metals from mine waste, such as tailings, slag heaps, and waste dumps. The Laboratory Technician Role: Carrying out preparation of samples for analysis. Performing analysis using XRF / ICP / other techniques as required. Recording and reporting test results. Maintaining good laboratory practice and the highest standards of housekeeping and safety. Performing laboratory admin and housekeeping duties as directed. Assisting with bench-scale metallurgical test work as required. Your Background: Degree/HND/HNC in Chemistry, or relevant discipline. Experience of working in a laboratory. Experience with using ICP and / or XRF for chemical analysis. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference (phone number removed) in all correspondence.

CK Group are recruiting for a Shift QC Technician, to join a multinational manufacturer of coatings and sealant at their site located in Shildon, County Durham, on a 3 month contract. The hours are 06:00-14:00 & 14:00-22:00 Monday - Friday with an hourly rate of 14.87 per hour uplifted to 17.23 per hour with shift allowance. Location: This role is located in Shildon, County Durham. QC Technician Role: The successful QC Technician will ensure the quality of the product manufactured and its accompanying documentation meets industry and customer requirements. You will be responsible for: Laboratory testing of paints and sealants to identify issues. Developing new formulations for specific customers. Supporting and investigating customer complaints. Liaising with other teams to ensure the product is fit for purpose. Your Background: To be considered for this position, you will have the following qualifications, skills and experience: Qualification in a Chemistry-related subject. Experience working in a laboratory environment (either academic or industrial laboratory). Good verbal and written communication skills. This is a fantastic opportunity for a QC Technician to join this global brand that works with some of the biggest names in aerospace. Apply: For more information, or to apply for this QC Technician please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only). It is essential that applicants hold entitlement to work in the UK. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

Talentmark are recruiting for a Waste Operations Chemist to join an Environmental and Waste Management company at their site based near Darrington on a full time, permanent basis. The salary for this role ranges from 28,000 to 35,000 per annum, dependent on experience. The Company: A leading UK waste and resource management company, our client is part of a global group with a strong heritage in providing services for communities and businesses. Their aim is to be the environmental company of choice, delivering change for a sustainable future. The company's core business focuses on collection, resource recovery and renewable energy providing services for local authorities and commercial customers. They have a number of core services including municipal services, business waste solutions, recycling and green energy. Location: The Operations Chemist will be based at the company's site near Darrington, easily commutable from Wakefield, Knottingley, Castleford, Leeds, Bradford, Doncaster and Scunthorpe. Operations Chemist Role: Your main duties will be: Chemical and Physical analysis of Waste. Inspection and testing of waste for acceptance. Interpretation of laboratory results. Maintenance, QC and Calibration of laboratory equipment. Ensuring safety procedures are always upheld. Your Background: The ideal candidate for this role will have the following skills and experience: Chemistry Degree/HND. Waste/Water testing experience using spectrophotometry. Hazardous Waste classification and consignment experience. Entitlement to work in the UK is essential. For more information or to apply for this Operations Chemist position, please contact Tehmina Sepai on (phone number removed) or email (url removed). Please quote reference (phone number removed). 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 url removed)/) and follow us to see our latest jobs and company news.

Associate Director, Toxicology Warrington Site-Based Talentmark is supporting a leading scientific services organisation in the search for an experienced Associate Director, Toxicology to lead and develop a high-performing toxicology function within a highly regulated environment. This is a senior leadership opportunity for an experienced toxicology professional with a strong leadership and strategic background. The successful candidate will support in the delivery of forensic toxicology services to the UK Criminal Justice System, and oversee toxicology operations, quality, R&D and continuous improvement initiatives, while helping shape the future direction of the function through innovation, automation and technology-driven efficiencies. Key responsibilities: Leading and developing multidisciplinary toxicology teams. Supporting strategic planning, operational delivery and business growth. Driving quality and compliance in line with international standards. Managing technical projects, budgets and performance KPIs. Building strong relationships with customers, regulatory bodies and external stakeholders. Supporting the implementation of new technologies and process improvements. Contributing to the delivery of high-quality forensic toxicology services in support of criminal investigations. Working closely with quality and compliance teams to maintain robust QA and QC systems. Representing the toxicology function at senior leadership and performance review meetings. Your Background: Significant experience and track record within a technical, highly regulated environment such as toxicology, pharmaceuticals, healthcare, clinical trials or scientific services. Strong proven leadership and people management experience. Degree in Toxicology or a related scientific discipline. Knowledge of international quality systems and regulatory standards. This is a full-time, site-based role in Warrington offering the opportunity to play a key role in a growing and impactful scientific organisation. Why Apply: Salary: 70,000 - 95,000 DOE Lead a high-performing toxicology team in a senior leadership role. Drive innovation, automation and continuous improvement. Influence strategy within a highly regulated scientific environment. Make a real impact by supporting forensic services for the UK Criminal Justice System. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence.

Talentmark are recruiting for a QC Microbiology Analyst to join a Pharmaceutical Services Company in Central Belt Scotland. This is a permanent role with Mon-Fri day time working hours and is site based. The Role: You will undertake the tasks and analytical processes involved in method feasibility/development/validation, day to day analysis, data interpretation and documentation of samples for microbiology analysis. Responsibilities: Undertake microbiology analysis and quantitative interpretation of any resultant data generated following defined protocols and procedures. Generate analytical reports and certificates of analysis for any data generated. Complete all assigned work to the appropriate level of science, quality and regulatory compliance. Present a professional manner at all times when dealing with internal and external customers. Carry out all work to the requested specifications and timescales. Ensure all work undertaken meets with the prescribed requirements of the Quality System and the requirements of cGMP. Your Background: Educated to degree level in Microbiology or a related field. Strong Microbiology laboratory skills with the ability to work independently and as part of a team. Experience of Aseptic Technique and experience in a pharmaceutical industry laboratory Experience of working to cGMP. Knowledge of QPulse QMS would be beneficial. Excellent attention to detail, communication and documentation skills. Apply: It is essential all applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence.

Talentmark are recruiting for a Quality Operations Manager, to join a well-established and successful global pharmaceutical company, based in Hatfield, Hertfordshire, on a permanent basis. Role: This role is responsible for Quality Operations and Quality Assurance activities, ensuring GMP compliance and quality system support for the manufacture, packaging, testing, storage, and distribution of marketed drug products. Key duties will include: Ensure quality system procedures and processes meet corporate, regulatory, and industry requirements and promote site adherence to them. Support site compliance activities, including implementation of new GMP requirements and inspection readiness programs. Support and (where required) lead Quality Operations planning and provide QA oversight for QC and Production activities to enable timely batch review, release, and distribution. Perform batch review of site and non-site manufactured batch records, as required. Monitor and report Quality Management System performance metrics and KPIs. Input and lead Quality Management Review meetings (as required.) Represent Quality Operations during regulatory inspections, customer audits, and third-party audits and support internal and external audit programs. Lead the Product Quality Review (PQR) program, including trend analysis and reporting. Author, review, and approve SOPs and other quality documentation such as PQRs, deviations, complaints, investigations, CAPAs, change controls, and qualification/validation documentation. Maintain and enhance the TrackWise Quality Management System, ensuring compliance with GxP and electronic records requirements. Deliver GMP and quality systems training, coaching, and mentoring to site personnel. Your Background: Educated to degree level or above in a science discipline with extensive previous experience in a Quality Management or Quality Assurance leadership role within the pharmaceutical industry. Extensive knowledge of Quality Assurance, Quality Systems, GMP, GDP, and pharmaceutical manufacturing and packaging processes. Experience with overseeing, maintaining and improving Quality Management Systems. Strong understanding of global GMP regulations and guidelines, with the ability to interpret, implement, and maintain compliance requirements. Proven ability to build effective relationships and collaborate across functions, sites, affiliates, and external partners. Strong communication and influencing skills, with the ability to engage stakeholders at local, regional, and global levels. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference (phone number removed) in all correspondence.

Talentmark are recruiting for a Data Analytics Operations Manager to join a global animal health company on a contract basis for 12 months. This is a hybrid role with 2 days per week on site in Bracknell. Salary: 350 to 450 per day Data Analytics Operations Manager Role: Lead risk assessment, review, control and reporting activities at the medicinal product level with key stakeholders in clinical trial teams Utilise up-to-date data from multiple medicine sources to identify quality risks Guide medicine business partners in developing mitigation plans to address identified risks Responsible for reporting risk management information to key stakeholders throughout the product lifecycle Your Background : Hold a degree in a scientific subject or have equivalent working experience. Working experience in GxP environment within the pharmaceutical industry. Proven knowledge in project management including experience in quality risk management. Proficient experience with clinical trials, clinical research associate, clinical trial management. Demonstrated experience in leadership and strategic problem solving paired with good knowledge about processes and quality management. Company: Our client is a leading manufacturer of vaccines, parasiticides and pharmaceuticals to protect animals. They are also one of the fastest growing animal health companies in the UK. Apply: For more information, or to apply for this Data Analytics Operations Manager please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only) . It is essential that applicants hold entitlement to work in the UK Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.