Remotely
documentationroot cause analysisgmphplcwet chemistryexception reports
Job Description
📋 Description
- Carry out quality control testing of pharmaceutical samples and biopharmaceutical products to
- Perform routine and non-routine analysis with accuracy and efficiency.
- Complete test records on time, ensuring SOPs and regulatory standards.
- Identify opportunities for quality and service improvement; contribute to CI projects.
- Adhere to GMP guidelines and internal quality standards; ensure activities are documented and
- Participate in Root Cause Analysis and prepare Exception reports.
🎯 Requirements
- 6 months to 1 year GMP experience
- Strong attention to detail
- Good knowledge of HPLC and wet chemistry testing
- Organized, accurate, and strong documentation skills
- Good understanding of GMP
- Ability to work independently and in a team
🎁 Benefits
- Developmental opportunities and career progression
- Private Medical Insurance after 2 years
- Income protection and life assurance
- Free parking onsite
- Additional annual leave days with continued service
- Work-life balance
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