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Johnson & Johnson is recruiting for a QA Associate supporting the Distribution Center, located in Beerse, Belgium.

The distribution center is a key player in multiple supply chains, acting as European DC for controlled substances, Worldwide Distribution Center supporting clinical trials and supporting our CAR-T manufacturing sites in Ghent.

In this role, you will play a critical part in ensuring compliance of both distribution and manufacturing activities, including repack and labeling and taking an active role in managing our QMS-associated processes. You will be working closely with several departments, including our operational team, Clinical Supply Chain, CAR-T, CQ EMEA and several others on a local and regional level.

You will also support investigations, root cause analysis, and change controls. Additionally, you will have the opportunity to lead projects linked to continuous improvement, increased compliance, and efficiency.

Key Responsibilities:

• Support in-depth investigations by providing quality and compliance expertise and ensuring the correct root cause and corrective actions are determined
• Perform batch record review related to repack activities completed at DC Beerse
• Act as QA representative in local and regional projects and ensure actions are properly documented in Change Controls
• Own the QMS processes applicable to DC Beerse team
• Maintain oversight of the QA specific parameters related to training, investigations, CAPA, change controls and audit follow-up
• Create and lead projects related to continuous improvement, increased compliance and/or efficiency
• Support the preparation, execution and follow-up of inspections and audits
• Establish and maintain effective working relationships with the different business partners to ensure the implementation and maintenance of harmonized and robust processes
• Support the operational and QA departments by providing coaching and/or training

Qualifications

Experience and Skills:
Required:

• A Master's degree in Pharmaceutical sciences, Biomedical sciences or similar scientific studies is required.
• Fluent in Dutch and English
• Motivated and eager to learn
• Strong analytical thinking and decision-making skills
• Works well in a team
• Able to work in a dynamic organisation and identifying the right priorities
• Strong interpersonal skills

Preferred:

• Experience with Comet, Tru Vault, Summit, QMS-processes
• Experience working in a GMP or GDP-regulated environment

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. We value diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. We are also committed to providing reasonable accommodations to individuals with disabilities. If you require a reasonable accommodation to apply for a position, please contact our Talent Acquisition team.