A multinational biopharmaceutical client in Berkshire is seeking an experienced Senior Process Quality Excellence Specialist. The role entails developing clinical quality systems and ensuring compliance with regulations such as GCP and GLP. Candidates should have over 8 years of pharmaceutical experience and be skilled in SOP writing. This contract position is offered for 12 months on a hybrid...
PME Engineer – Building Management Systems (BMS) Ireland - Hybrid Working Salary - €50,000 - €60,000 + Package + Bonus About the Role A leading engineering organization is seeking a PME Engineer with strong Building Management Systems (BMS) experience to support the design, implementation, and optimization of building and utility control systems. This role plays a key part in ensuring safe,...
Job Description Role Overview This role supports Quality Control raw materials activities within a regulated manufacturing environment. The position focuses on delivering accurate, compliant analytical work to agreed timelines, while maintaining high quality standards and supporting team performance. The role holder will manage their own workload with guidance from senior staff and contribute...
Qualified Person (QP) – Pharmaceutical Manufacturing & Quality Industry: Global Pharmaceuticals / Life Sciences Location: London, United Kingdom (On-site / Manufacturing & Corporate Quality Office) Type: Full-Time, Permanent Salary Band: £90,000 – £110,000 + Benefits Experience Level: Senior (8–15 Years) The Role (Why This Exists): We are supporting a global pharmaceutical organisation...
Role Overview: Salary: From £50,000 per annum - depending upon experience Hours: 0900 – 1800, weekdays Location: Holborn, London Contract: Opportunity for flexible days/contract based role Role Summary: The CQC Compliance Manager role is an essential part of the Clinic, supporting the Senior Leadership Team, acting as the day-to-day lead for all matters related to the Care Quality...
You will be responsible for: - Driving a positive Quality culture throughout the facility, assisting with continuous improvement activities on site. - Ensuring all manufacturing, testing and release activities are carried out in accordance with current GMP regulations. - Carrying out Qualified Person's batch release responsibilities of the company's various products.
Inspection Readiness Manager, 12-month contract UK or Ireland Company Name: Vertex Pharmaceuticals Type of Role: Contract position Contract length: 12 months Location: Hybrid (3 days on site in Paddington, London or Dublin, Ireland) Department: Quality Standards Management Reporting into: Inspection Readiness Associate Director Looking for opportunities with purpose, impact and...
About MasterControl: MasterControl Inc. is a leading provider of cloud-based quality and compliance software for life sciences and other regulated industries. Our mission is the same as that of our customers to bring life-changing products to more people sooner. The MasterControl Platform helps organizations digitize, automate and connect quality and compliance processes across the regulated...
You will act as an external arm of their clients, liaising with and managing CDMO's, and other key Vendors.
You will be speaking with key stakeholders including C-suite, and VP level, as well as connecting with entry level and specialists within their clients.
PE Global is currently recruiting for a Quality Specialist/Auditor for a leading multi-national Pharma client based in Moorgate, London. This is an initial 6 months contract position offering hybrid work. 37.5 hours per week. Pay Rate is from £17.79ph up to £26.51ph PAYE. Depending on experience. ***Please note our client cannot assist with any visa sponsorship and candidates must have the...
Head of Quality Assurance (CONTRACT - 1.0 FTE, 12 months) We’re partnering with a respected Biotech organisation in the UK seeking a consultant to become Head of Quality Assurance. What you’ll do: - Lead QA staff, including QP/RP roles where applicable. - Maintain and continually improve the GMP-compliant Quality Management System (QMS). - Ensure audit readiness and lead internal, supplier,...
Job Title: Qualified Person (QP) – Pharmaceuticals Location: London, United Kingdom (Onsite) Work Arrangement: Onsite – Plant / Quality Office (No remote work) Work Schedule: Standard business hours (Full onsite presence required) Employment Type: Full-Time | Permanent Role Overview We are seeking an experienced Qualified Person (QP) to ensure that medicinal products released to the UK and...
You will also report on inventory levels, deliver data to inform strategic decisions, and work cross-functionally to improve operational efficiency and maintain high product quality while supporting the Supply Chain & Ops Associate and Head of Supply Chain and Operations. What we want you to do
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind...
Quality Assurance / Quality Control (QA/QC) Technician Slough | Food Production £15 per hour We are recruiting a hands-on Quality Assurance / Quality Control professional to join a well-established, independent food manufacturer based in Slough. This is a great opportunity for someone with QA or QC experience who enjoys being involved in production, maintaining high standards, and ensuring food...
You will lead customer audits, manage key quality processes, and contribute to site and global quality projects that drive continuous improvement.
You will lead the QA team, maintain GMP-compliant systems, and ensure audit readiness while managing internal and external audits. The ideal candidate will have proven QA leadership experience, excellent communication skills, and a solid background in regulatory compliance. This is a 12-month contract role with opportunities to influence quality across the organisation.
Role Overview This role supports Quality Control raw materials activities within a regulated manufacturing environment. The position focuses on delivering accurate, compliant analytical work to agreed timelines, while maintaining high quality standards and supporting team performance. The role holder will manage their own workload with guidance from senior staff and contribute to continuous...
Job Title: Associate Director, Asset Engineering Location: Slough, UK (with regular travel to Cambridge). Hybrid working available for eligible activities. The actual location of this job is in Slough, UK, with travel to Cambridge. Relocation assistance is available for eligible candidates and their families, if required. Today, Lonza is a global leader in life sciences operating across five...
Job Title: Senior Purification Scientist Location: Slough Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big...