GMP Manufacturing Scientist - 12 month contract
On-siteNottingham, England, United Kingdom
Job Summary
Prepare manufacturing documentation, including Batch Manufacturing Records, labels, and cleaning procedures, while setting up processing rooms and equipment for GMP production. Manufacture pharmaceutical products for clinical studies in accordance with GMP standards, SOPs, and Good Documentation Practice. Support method development, validation, and transfer activities, ensuring accurate records for full traceability. Carry out cleanroom activities, manage controlled disposal of supplies, and communicate progress to Production, QA, and Project Management teams. This hands-on role within the Nottingham team focuses on the safe delivery of Investigational Medicinal Products across the development pathway.
Required Qualifications
- A degree in a science subject, or equivalent relevant experience in a GMP, GLP, pharmaceutical, manufacturing or laboratory setting
- Strong attention to detail and a high level of accuracy
- Ability to follow written procedures, SOPs and protocols
- Good documentation skills, with an understanding of the importance of clear and traceable records
- Good organisation skills and the ability to manage a varied workload
- A proactive and responsible approach to safety, quality and compliance
- Good communication skills and the ability to work well as part of a team
- aged 18 years or over
- not have been debarred by the FDA
Desired Qualifications
- Experience in GMP manufacturing or pharmaceutical production
- Experience in clinical trial manufacturing or IMP manufacture
- Experience working in a cleanroom or controlled environment
- Knowledge of Batch Manufacturing Records, COSHH, swabbing, validation or cleaning procedures
- Awareness of radiolabelling, radiation safety or radioactive isotope handling
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