A leading life sciences company in Slough is seeking a Biotechnologist 1 for the night shift. This entry-level position offers hands-on experience in a GMP manufacturing environment, focusing on the safe and efficient production of life-changing products. Key responsibilities include adhering to GMP practices, engaging in production tasks, and fostering a safety-first attitude within the team....
A leading biotechnology firm based in Slough, UK, is seeking a Biotechnologist 1 for the night shift. In this entry-level role, you will gain hands-on experience in GMP manufacturing, implement safety and production protocols, and contribute to continuous improvements in the production process. The ideal candidate should have manufacturing experience, a good command of English, and strong...
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,...
The Qualified Person (QP) will be responsible for ensuring that each batch of medicinal product is manufactured and checked in compliance with applicable laws, EU/UK regulations, and Marketing Authorization requirements prior to release. The QP will act as the primary authority for quality, compliance, and batch certification, ensuring patient safety and regulatory adherence across UK/EU...
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...
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...
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...
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...
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.
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...
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,...
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
Senior Quality Engineer Medical Device Startup | £60M Raised Why This Role Matters This is a rare opportunity to join a high-growth medical device startup that has raised £60M from top-tier investors and is scaling rapidly towards global commercialisation. The company is building next-generation medical technologies that will meaningfully improve patient outcomes. As Senior Quality Engineer,...
Operational Technology Team Lead (50% Team Lead/ 50% SME) 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....
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: Quality Auditor / QA Specialist – Contract (6 Months) Location: London (Hybrid – 2–3 days on-site) We are seeking an experienced Quality Auditor / QA Specialist to join a global pharmaceutical development team on a 6-month contract. This role offers exposure to a wide range of investigational medicinal products, from small molecules to complex biologics, and an opportunity to make a...