26 to 47 of 47 Permanent GMP Jobs

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 ❯

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 ❯

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 ❯

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 ❯

for usability, performance, quality, and manufacturability. Use CAD software (preferably SolidWorks) to create models, drawings, and layouts. Ensure compliance with applicable medical device regulations and quality systems (e.g., ISO, GMP, GLP). Partner with Legal and IP teams to identify and support opportunities for intellectual property protection. Minimum Requirements: Education Bachelor's degree in Engineering or a related field. Work … development. Strong ability to manage and execute design objectives independently. Proficiency in CAD (SolidWorks preferred). Experience with design tools such as FEA, DFSS, DFM, ISO/CE Mark, GMP, GDP, ASME Y14.5, and GD&T. Knowledge plastic film processing, pressure-sensitive adhesives, and other medical-grade materials. Understanding of regulatory standards (ISO 13485, ISO 14971, IEC 60601). Strong More ❯

used in pharmaceutical packaging. Responsibilities include on-site service, vendor coordination, project materials management (SAP/CRM), customer training, line audits, and system upgrades. Ensure compliance with SHEQ and GMP standards while supporting both European and U.S. equipment. Requirements Associate degree + 3-5 years' experience or 8+ years in a GMP environment Strong knowledge of PLCs, HMIs, SCADA, and More ❯

opportunity to be part of a company that values innovation, collaboration, and the flawless execution of ideas that genuinely improve the world! Key responsibilities: Generate and revise documentation for GMP manufacturing to ensure technical accuracy and GMP compliance. Provide technical support to develop required process documentation in collaboration with internal customers. Independently manage the creation of new documents and revise … GMP documents according to detailed procedures. Use and maintain the Documentation Management System (DMS) according to detailed procedures. Produce and process batch documentation according to standard timelines, coordinate review, approval, and issuance ensuring availability for use in Manufacturing per production schedule. Monitor progress of document creation and communicate with relevant parties to resolve potential issues in a timely manner. Manage … training to others during routine document revision. Understand and align with company policies, departmental practices, regulatory, and statutory requirements. Key requirements: Proven experience as a Technical Writer in a GMP manufacturing environment. Outstanding ability to generate and revise technical documentation with attention to detail. Comprehensive knowledge of DMS and standard methodologies for documentation. Ability to manage multiple tasks and projects More ❯

recruit an Associate Expert Bioprocess DSP (m/f/d) to join the Pilot Plant Downstream Process team starting at the next possible date at our Research and GMP Production Site in Heidelberg. Associate Expert Bioprocess DSP (m/f/d) What's the best thing about working with us? A permanent position in full-time (40 hrs. … development and process transfer from laboratory to pilot scale Planning and execution of DSP unit operations at pilot scale in technical and clinical campaigns (cleanroom class D + C, GMP regulated environment) Development and implementation of new process technologies within the framework of process optimization Creation of process risk analyses, control strategies, process mappings, batch protocols, development plans, and reports More ❯

We are currently recruiting for a QA Supervisor based at our Llanidoles site, this will be a 5 day onsite role. The successful candidate will be responsible for leading a small QA team to ensure the efficient and effective operation More ❯

GMP Recruitment are proud to be in partnership with a long-established and reputable defence engineering firm based in the Birmingham area. We are currently recruiting on their behalf for an experienced IT Support professional to join their I.T Department on a full-time, permanent basis. This position offers a salary of up to £35,000 Per annum based on … obtain BPSS and SC clearance. AN IMMEDIATE START IS AVAILABLE FOR SUCCESSFUL CANDIDATE. If the above role sounds perfect for you, or you require more information, please click apply. GMP Recruitment are recruiting for this role on behalf of their client and are acting as an Employment Agency. More ❯

Work on the cleaning crew on weekends as needed Working knowledge of HACCP plan and HACCP checks Working knowledge of SOP plans and SSOP checks LOTO trained Know all GMP's and plant rules Must know how to GMP audits Water and ice monitoring-help collect samples and send to lab E-Coli Sampling procedure Complete various checks, collections, and More ❯