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Location: Hoofddorp Duration: 1 year (extension is possible) Language: English Industry: Pharma Start date: 1-10-2022
The company Our client is a biopharmaceutical company engaged in the development of cancer immunotherapies with the aim to provide long term response and eliminate this chronic disease.
About the role As a Quality Assurance Specialist you will be responsible for ensuring the accuracy and completeness of the QA issued documents.
Responsibilities - Control the issuance of batch document and label packages including the final product labels per cGMP - Identify and escalate compliance gaps across the controlled issuance process -Support Audits (internal, external) - Execute strategic initiatives to improve the controlled issuance process - Controlled the issuance of logbooks
Requirements - 2+ years’ experience on document management in a regulated environment - Advanced level of English communication - Ability to effectively communicate with peers.
Ready for the next step in your QA career? Reach out to me by applying to this vacancy.
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