Quality Control Analyst

Leiden, 1-year contract, 40h, Hybrid way of work 

Johnson & Johnson Worksense is responsible for finding, engaging, and contracting talent for the Johnson & Johnson contingent workforce.

We are currently recruiting a Quality Control Analyst to join our contingent workforce in Janssen in Leiden for a 12-month contract. 

You will be working in a team of ten colleagues, that is exclusively concerned with the QC aspects of clinical and commercial raw materials.

Responsibilities

• Act as lead investigator for local/global Non-Conformances which encompasses conducting the investigation, providing impact assessments, and identifying and defining appropriate corrective and preventive actions.
• Support and advise other investigators from external and internal QC departments.
• Monitor timely closure of medium/high-level investigations and associated Corrective & Preventive Actions.
• Review of the release packages coming from internal and external contract laboratories.
• Resolve deviations identified in the release package, by performing the corrections yourself or coordinating the implementation of the corrections by other teams e.g., Global Planning, Warehouse, and external contract laboratories.
• Release of the raw materials in SAP, our enterprise resource planning system.
• Serve as an expert on physical and chemical technologies used for raw materials testing and will be requested to represent the team during internal/external meetings. 
• Lead or participate in exciting projects or studies to maintain the quality of the testing of the raw materials.
• Lead and drive continuous improvement processes to contribute to lean culture in the area of testing and to improve our cost competitiveness.
• Transfer of new analytical techniques to the (external) testing laboratories, in close corporation with our USA-based development team.
• Design an optimal test strategy for new materials to reduce the time between the arrival of material and the release for usage.

To be successful in this role you have:

• A university degree (bachelor's, master or Ph.D.) in Analytical Chemistry, Pharmacy, or equivalent
• 3-5 years of experience in a Quality Control environment with demonstrable knowledge of pharmaceutical raw materials and associated regulations
• Knowledge of GMP/GLP guidelines
• Proven capabilities in managing smaller and/or larger projects
• Result-oriented, team player, self-starter
• Excellent communication skills (oral and written in English) 

If you meet our requirements and are interested in hearing more about our Quality Control Analyst role, please do not hesitate to apply through the provided link today and a member of our recruitment team will be in touch!

For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.

We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences.

That is why we in the Netherlands are working to create an inclusive environment where diverse backgrounds, perspectives, and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.

Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”!