5 of 5 Remote GMP Jobs in the North of England

as extensive technical training will be provided. Proven experience in leading complex MES projects from concept to deployment. Knowledge and understanding of Pharma and Biotech industry & processes. Familiarity with GMP, FDA 21 CFR Part 11, GAMP5, and other relevant regulatory requirements. Excellent problem-solving, communication, and interpersonal skills. Ability to travel as required to client sites. What We Offer: Competitive 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 experience ideally across all digital media channels but in particular paid search. You will have excellent knowledge of bid management and core technology platforms such as Google Analytics, GMP Platform, SA360 for example. Data analysis and an understanding of the strategic application of digital marketing channels will be a strength. More ❯

We are seeking a Supplier Quality Audit Lead within the Central Supplier Quality Audit and Compliance team, supporting the global supply chain. The role involves planning, executing, and documenting GMP audits, managing supplier action plans, and supporting change controls. Responsibilities Perform GMP and Quality System assessments of suppliers and recommend approval statuses. Agree on CAPA plans and ensure their timely … risks, escalate high-risk issues, and support inspections. Candidate Profile Basic Qualifications & Skills Experience in regulated environments like pharmaceutical manufacturing. Degree in Life Sciences or related fields. Knowledge of GMP requirements and QMS principles. Proficiency in English. Preferred Qualifications & Skills Experience with API, sterile, parenteral, or biopharmaceutical manufacturing. Auditor certification from relevant organizations. Application Details Deadline: Sunday 31st August. Please More ❯