26 to 50 of 60 GMP Jobs

continuous improvement in patient outcomes. Your new role As QA Compliance Manager, you'll lead a team responsible for maintaining and improving the Quality Management System in line with GMP, ISO, and regulatory standards. Reporting to the Head of Quality, you'll oversee internal audits, batch record reviews, CAPA systems, and customer audits. You'll also contribute to strategic quality … Qualified Person (QP) sponsorship for the right candidate. What you'll need to succeed A degree in a scientific discipline (e.g. Chemistry, Biology, or related field) Extensive experience in GMP-regulated environments (10+ years preferred) Strong leadership and people management skills In-depth knowledge of EU cGMP and ISO standards (9001, 13485) Experience supporting or conducting batch release under QP More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

pension rectification projects. Location: London, Reigate, Bristol, Birmingham, Manchester, Leeds, or Edinburgh Work Style: Hybrid and flexible options available The Role: Design and tailor bulk data rectification approaches for GMP and other correction projects Communicate complex technical issues to various internal and client audiences Demonstrate sound judgement in balancing the need for accuracy and pragmatism in solutions Guide a team More ❯

Unix-based operating systems, use of the command line and SQL is advantageous but not essential as training will be provided. Strong knowledge of Contracting Out Requirements such as GMP Strong Defined Benefit Knowledge, including historical knowledge of UK Pensions Legislation. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy. More ❯

ll devise and deliver best in class data services, develop effective data strategies, and manage technical pension rectification projects. The Role: Design and tailor bulk data rectification approaches for GMP and other correction projects Communicate complex technical issues to various internal and client audiences Demonstrate sound judgement in balancing the need for accuracy and pragmatism in solutions Guide a team More ❯

ll devise and deliver best in class data services, develop effective data strategies, and manage technical pension rectification projects. The Role: Design and tailor bulk data rectification approaches for GMP and other correction projects Communicate complex technical issues to various internal and client audiences Demonstrate sound judgement in balancing the need for accuracy and pragmatism in solutions Guide a team More ❯

ll devise and deliver best in class data services, develop effective data strategies, and manage technical pension rectification projects. The Role: Design and tailor bulk data rectification approaches for GMP and other correction projects Communicate complex technical issues to various internal and client audiences Demonstrate sound judgement in balancing the need for accuracy and pragmatism in solutions Guide a team More ❯

ll devise and deliver best in class data services, develop effective data strategies, and manage technical pension rectification projects. The Role: Design and tailor bulk data rectification approaches for GMP and other correction projects Communicate complex technical issues to various internal and client audiences Demonstrate sound judgement in balancing the need for accuracy and pragmatism in solutions Guide a team More ❯

ll devise and deliver best in class data services, develop effective data strategies, and manage technical pension rectification projects. The Role: Design and tailor bulk data rectification approaches for GMP and other correction projects Communicate complex technical issues to various internal and client audiences Demonstrate sound judgement in balancing the need for accuracy and pragmatism in solutions Guide a team More ❯

Developing specifications and leading multidisciplinary teams to clearly communicate the requirements for the Store and capture client requirements. The industries we serve have growing requirements for regulatory quality control (GMP, Medical Devices, ISO etc). The System Engineering role provides opportunity to develop the fully documented lifecycle to support adherence to these standards. What You'll Be Doing Designs, defines More ❯

Excel Knowledge of technical actuarial concepts, specifically principles underlying bulk annuity pricing Awareness of DB buy in/buy out market, life insurance/relevant regulation. Any experience of GMP would be a distinct advantage Support Head of True up, DB Actuary and DB Senior Actuarial Analyst in accurate and timely delivery of data true ups. Carry out all necessary More ❯

Excel Knowledge of technical actuarial concepts, specifically principles underlying bulk annuity pricing Awareness of DB buy in/buy out market, life insurance/relevant regulation. Any experience of GMP would be a distinct advantage Support Head of True up, DB Actuary and DB Senior Actuarial Analyst in accurate and timely delivery of data true ups. Carry out all necessary More ❯

regulated manufacturing environment. This opportunity is ideal for someone with a science or pharmaceutical-related degree and exceptional people management skills, looking to make a meaningful impact in a GMP-licensed facility. Key Responsibilities: Lead and manage a team of QA Officers to ensure product release meets GMP and QMS standards. Support the QA Manager with site inspections, internal audits … risks are mitigated. Experience: Degree in Microbiology, Biology, Biomedical Sciences, or equivalent. Pharmacy Technician Level 3 (GPhC registration desirable). Proven experience in pharmaceutical manufacturing and working within a GMP-regulated environment. Strong leadership and coaching skills with a track record of team development. Excellent understanding of MHRA regulations, ISO standards, and quality systems. Skilled in risk management, root cause More ❯

instructions, change controls, deviations, investigations, validation, customer audits/quality requests, and material and product disposition. The QA officer is expected to identify, escalate and work to address any GMP/GxP issues with potential impact to product quality or quality compliance. Together we offer fantastic opportunities for committed employees to learn and develop their career with us. At Piramal … to performing the relevant disposition of products. Where potential issues exist, these are to be highlighted to the QA manager. Promote and work to ensure compliance with all relevant GMP/GxP requirements. Support and lead as required, quality process improvements and quality management system improvements within the department and on site. Escalate any identified GMP/GxP areas of More ❯

the functioning of the QMS, providing oversight to key stakeholders alike (including senior staff members). Accountability across (but not limited to); change control, stability, documentation control, internal audits, GMP, supplier approval, complaints, PQRs, NPI, route cause analysis and controlled drug returns. Ensuring compliance/correct documentation practices, i.e batch records, laboratory tests and quality agreements too. Overseeing supplier verification … batch review process. Keeping abreast of evolving UK & EU retained regulations (for the purposes of pharmaceutical and/or food/ingredients manufacturing). To ensure compliance with EU GMP standards & BRC food safety requirements. Managing the preparation process (and heavily involved in hosting activities) for MHRA inspections, customer (third party audits) and acting as the lead person. Enrsuring quality … bodies. Deputising for the HOQ when required. The Person:- The ideal Candidate will hold a degree in a STEM related subject Experience managing QA team/s in an GMP/Pharmaceutical setting. Management experience essential (will consider Team Leader or similar). Experienced in batch review and batch release Experience in auditing and audit hosting Experience in CAPA, deviations More ❯

of growth, assisting the Quality team with improvement projects and manging the QMS through a busy period. The Role: As a QA officer, you will: Maintain the QMS, ensuring GMP, GLP and data integrity compliance. Support QA activities, including QA review & release of data, Change controls, Document review & distribution and implementing CAPAs. Investigate OOS, deviations and complaints. Assist internal audits … maintaining audit readiness. Required: A degree or similar qualification in a relevant scientific field. Proven QA experience in a GMP/GLP Environment. Experience in supporting, preparing for or leading internal/External audits. Experience of investigation OOS, Deviations & Complaints Validation Experience would be highly advantageous. Attention to detail and the ability to manage multiple priorities. SRG are the UK More ❯

customers and answering queries and product investigations Coordinate and resolve immediate/urgent customer complaints, ensuring prompt responses/resolution Participate in the internal audit programme to ensure continued GMP compliance of all site activities Utilise scientific resources in order to work on improving quality of products and services To maintain personal training folder in an auditable state Maintaining quality … limited to: Risk Assessments Change Controls CAPAs Deviations Complaints Recalls OOS/OOT Key Requirements: Will have a Degree in a relevant- Scientific discipline Will have good knowledge of GMP Experience in CAPA, Deviations, OOS, OOT, Internal auditing (preferred), Customer Complaints handling would be very advantageous Strong IT skills (Microsoft applications) Good interpersonal skills and strong written/verbal report More ❯

and improved upon, whilst taking a lead in generating and building a quality culture. Role Accountabilities: To participate and direct QA team to observe and audit production processes and GMP, ensuring products are made to specification and within customer codes of practice and Bakkavor standards - reporting findings to managers as appropriate To assist in delivery of site standards for visits … correct standard With guidance from Line Manager, manage QA activities required to deliver improvement of Technical KPIs e.g. audit of non-conforming processes, complaint investigations, update of swab schedules, GMP audits, glass, and plastic audits To plan and co-ordinate work of the QA team to meet requirements of the quality management system and the needs of the business ensuring More ❯

and improved upon, whilst taking a lead in generating and building a quality culture. Role Accountabilities: To participate and direct QA team to observe and audit production processes and GMP, ensuring products are made to specification and within customer codes of practice and Bakkavor standards - reporting findings to managers as appropriate To assist in delivery of site standards for visits … correct standard With guidance from Line Manager, manage QA activities required to deliver improvement of Technical KPIs e.g. audit of non-conforming processes, complaint investigations, update of swab schedules, GMP audits, glass, and plastic audits To plan and co-ordinate work of the QA team to meet requirements of the quality management system and the needs of the business ensuring More ❯

GMP Recruitment are proud to be partnered with one of the UK’s leading and fastest-growing manufacturers for the aerospace industry. We are supporting our client by recruiting for an ERP System Specialist to join their site on a full-time, permanent basis. This is a standalone position offering a competitive salary of £40,000–£50,000, plus excellent … ability to act strategically while ensuring delivery at an operational level. If the above position sounds perfect for you, or you require more information, please click apply or contact GMP Recruitment directly. GMP Recruitment are recruiting for this role on behalf of their client and are acting as an Employment Agency. More ❯

Quality Assurance Officer on a 12-month fixed term contract. This is a great opportunity to join a well-established team and support key QA activities in a regulated, GMP environment. The Role: Support day-to-day QA operations, ensuring compliance with SOPs and GMP Assist with supplier quality management and document control Help implement global quality procedures at site More ❯