Manufacturing Scientist
Posted 2 weeks ago by Cpl Life Sciences
Negotiable
Inside
Undetermined
Liverpool, England, United Kingdom
Summary: CPL Life Sciences is seeking a Manufacturing Scientist for a 12-month temporary role in the pharmaceutical industry, based in Liverpool. The position involves overseeing finished products, managing GMP documentation, and supporting production processes to ensure quality and compliance. The ideal candidate should possess relevant qualifications or experience in life sciences or engineering and be fluent in English.
Key Responsibilities:
- Provide expertise within packaging and materials
- Participate in meetings, ensuring compliance with standards
- Maintain oversight of SOPs
- Support with writing of technical reports
- Identify continuous improvement opportunities
- Support in managing process transfer projects
- Support NPI
Key Skills:
- University degree or hands-on experience in life science or engineering
- Fluent English
- Understanding of production environments
- Understanding of quality standards
- Multi-tasking/priority management
- Ability to author documentation in line with GMP standards
Salary (Rate): undetermined
City: Liverpool
Country: United Kingdom
Working Arrangements: undetermined
IR35 Status: inside IR35
Seniority Level: undetermined
Industry: Other
CPL Life Sciences are partnered with a client in the pharmaceutical industry, who are looking for a Manufacturing Scientist to join on a 12 month temporary basis (PAYE). This role will be based in the Liverpool area.
Role description: The Manufacturing Scientist will provide oversight for finished product. This position involves controlling of GMP documentation, supporting production processes to ensure quality and compliance.
Key duties:
- Provide expertise within packaging and materials
- Participating in meetings, ensuring compliance of standards
- Maintaining oversight of SOP's
- Support with writing of technical reports
- Identify continuous improvement opportunities
- Support in managing process transfer projects
- Support NPI
The ideal candidate will have:
- University degree or hands-on experience in life science or engineering
- Fluent English
- Understanding of production environments
- Understanding of quality standards
- Multi-tasking/priority management
- Can author documentation in line with GMP standards
If interested, please apply directly or send your CV to megan.smyth@cpl.com