QA Formulation Technician – Preparation Environments (Replacement Contract)

As a QA Formulation Technician – Preparation Environments (Replacement Contract), you will be responsible for ensuring the quality of GMP documentation, conducting quality reviews, and performing site work.

Your responsibilities include:

• Reviewing the quality of batch records and their closure within deadlines on paper and computer systems
• Ensuring procedures are followed correctly on site
• Conducting audits in production, investigations in collaboration with production, and identifying risks that may impact vaccine quality, efficacy, and safety
• Performing EHS audits on site
• Monitoring activities in Grade B areas
• Acting as the first GMP contact for aseptic zone practices
• Coordinating document flow between production and QA, verifying documentation in local premises
• Making adequate encodings for lot tracking and release (completing the QA GMP inspection plan)
• Regularly checking equipment in production areas
• Supporting GMP-type training
• Working daytime hours

To be considered for this role, you should:

• Hold a Bachelor's degree in a scientific field (Chemistry, Biochemistry, Biology, etc.) or an A2 (CESS) with over 10 years of valuable experience
• Ideally have previous similar experience (pharmaceuticals, laboratory, procurement, etc.)
• Demonstrate autonomy while evaluating risk situations
• Take decisions and responsibilities
• Be precise and rigorous
• Show perseverance
• Possess good teamwork and communication skills
• Have a critical and analytical mindset

GSK offers a competitive salary package, including a monthly gross salary starting at EUR 3,774, an annual bonus, and eligibility to participate in the company's share-based long-term incentive program.