Remotely
documentationquality controlroot cause analysisgmphplcbiologics testing
Job Description
📋 Description
- Carry out quality control testing of pharma and biopharma products
- Perform routine and non-routine analyses accurately
- Complete test records on time per SOPs/regulations
- Identify opportunities for quality and service improvements
- Adhere to GMP and internal quality standards; document activities
- Participate in Root Cause Analysis and prepare reports
🎯 Requirements
- 1 to 3 years GMP experience
- Strong attention to detail
- HPLC experience and exposure to biologics testing
- Organized, accurate with strong documentation
- Good GMP understanding
- Independent and team work ability
🎁 Benefits
- Developmental opportunities and career progression
- Private Medical Insurance after 2 years for all roles
- Income protection and life assurance
- Free onsite parking
- Additional annual leave with continued service
- Opportunity to work on life saving products
