Quality Control Analyst
Posted 1 day ago by PE Global
Negotiable
Undetermined
Undetermined
Dartford, England, United Kingdom
Summary: The Quality Control Analyst role at PE Global involves conducting Quality Control analysis to support production processes for a leading multinational pharmaceutical client in Dartford. The position requires flexibility due to a rotating shift pattern, including morning, afternoon, and night shifts. The analyst will perform testing and analysis in accordance with established methods and procedures while ensuring compliance with GMP and EHS standards. This is an initial 12-month contract position.
Key Responsibilities:
- Conduct Quality Control analysis to support production by testing in-process controls and composite samples.
- Perform analysis on analytical samples following defined methods and Standard Operating Procedures.
- Review, approve, and report generated data for QC Release as required.
- Ensure all analysis is conducted in accordance with company GMP and EHS procedures.
Key Skills:
- Knowledge/experience in particle size analysis.
- HPLC Method Development and Validation.
- Degree in a Scientific Biotech or similar.
- Experience in GMP environments.
Salary (Rate): undetermined
City: Dartford
Country: United Kingdom
Working Arrangements: undetermined
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
PE Global are currently recruiting for a QC Analyst for an initial 12 month contract role with a leading multinational pharma client based in Dartford. This position is based on a rotating shift pattern, including morning, afternoon, and night shifts. Flexibility is required.
Job Responsibilities
- To conduct Quality Control analysis in support of the smooth running of production by testing, in a timely manner, in process controls and composite samples under day to day supervision.
- To perform analysis on analytical samples in accordance with defined analytical methods and Standard Operating Procedures and within timelines as agreed with line management.
- Review, approval and reporting of generated data for QC Release as required by the role.
- To ensure all analysis is conducted in accordance with company GMP and EHS procedures.
Requirements
- Particle size analysis knowledge/experience
- HPLC Method Development and Validation
- Degree in a Scientific Biotech or similar
- GMP
Please click the link below to apply or send an up to date CV to veronica@peglobal.net
***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK***