Quality Control Analyst
Posted 1 week ago by SRG
Negotiable
Undetermined
Undetermined
Liverpool, England, United Kingdom
Summary: The QC Analyst – Biosafety role involves working in a regulated Quality Control laboratory within a global pharmaceutical manufacturer in Liverpool. The position is ideal for a Biological Science graduate with GMP experience, focusing on testing and compliance with regulatory standards. The role requires performing routine QC testing and documenting results accurately. This is a 12-month contract with a shift pattern of 4 days on and 4 days off.
Key Responsibilities:
- Performing a range of tests within a highly regulated Quality Control laboratory to GMP regulations.
- Performing routine QC testing.
- Documenting laboratory results in an accurate and timely manner.
- Complying with GMP regulatory requirements at all times.
Key Skills:
- Experience of working to GMP/pharmaceutical regulatory requirements is desirable.
- Biological background either from university degree or relevant work in the field.
- Computer skills, including Excel, Word, and Outlook.
- Preferable experience within cell cultures and/or assay testing.
- Familiarity with LIMS and SAP.
Salary (Rate): undetermined
City: Liverpool
Country: United Kingdom
Working Arrangements: undetermined
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
Job Title: QC Analyst – Biosafety
Location: Speke, Liverpool.
Contract: 12 months
Shift : 4 days on, 4 days off. 7am – 7pm.
SRG are currently working with a global pharmaceutical manufacturer based in Liverpool, looking for QC Analyst (Biosafety) to join the team. The site in Speke specialises in the production of sterile injectable products, for the treatment of the flu. This is a fantastic opportunity for a Biological Science graduate with some GMP experience to further their career.
Main responsibilities:
- Performing a range of tests within a highly regulated Quality Control laboratory to GMP regulations.
- Performing routine QC testing
- Documenting laboratory results in an accurate and timely manner.
- Complying with GMP regulatory requirements at all times.
Key requirements:
- Experience of working to GMP/pharmaceutical regulatory requirements is desirable.
- Biological background either from university degree or relevant work in the field
- Computer skills, excel, word, outlook
- Preferrable Experience within cell cultures and/or assay testing.
- LIMS and SAP