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About the Company
Our client is one of the biggest companies in  the biopharmaceutical industry. Their main purpose is to develop of cancer immunotherapies with the goal of provide durable response in a rapid and long-term way to save lives by finding the cure for cancer. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR).

The company is located in Hoofddorp, North Holland.

About the role
As a Quality Assurance Specialist you will be in charge of ensuring the precision and completeness of the QA documents.

Responsibilities
- Control the issuance of batch document and label packages per cGMP
- Identify and escalate compliance gaps across the controlled issuance process
- Support Audits (internal, external)
- Perform strategic initiatives to improve the controlled issuance process
- Controlled the issuance of logbooks

Requirements
- 2+ years’ experience on document management
- Advanced level of English communication
- Ability to effectively communicate


Are you ready for the next step in your career or you know someone who fits with the role? Please don't hesitate to apply clicking the button below!