Hoofddorp
jobid=A.0.174
Job Title: QA Specialist – Operational Review & Disposition
Location: Hoofddorp
Salary: €3,993 – €4,493
Quality Assurance (QA) Specialist I – Operations Review & Disposition
Are you passionate about quality and ensuring life-changing treatments reach patients on time? Join a leading biopharmaceutical company in Hoofddorp, where you’ll play a key role in reviewing manufacturing processes and preparing products for market release in a fast-paced, innovative environment.
What You’ll Do:
- Review manufacturing, environmental monitoring, and quality control data for in-process and finished products (both paper and electronic records).
- Compile product documentation to support quality assurance disposition and product release.
- Identify and report any deviations from approved processes.
- Assist with various QA activities to maintain compliance with industry regulations and company procedures.
- Perform administrative tasks related to quality assurance operations.
What We’re Looking For:
Skills & Knowledge:
- Basic understanding of Good Manufacturing Practices (GMP) and/or Good Laboratory Practices (GLP).
- Strong verbal, written, and interpersonal communication skills.
- Proficiency in Microsoft Office applications.
- Comfortable using computerized systems (e.g., ERP, EBR, LIMS) for manufacturing record reviews.
Education & Experience:
- With a Bachelor’s degree (BSc): At least 2 years of experience in a GMP environment.
- With an Associate degree (2 years undergraduate): At least 3 years of experience in a GMP environment.
- Experience in the pharmaceutical or biotechnology industry is a plus.
Interested?
Apply now by clicking “Easy Apply” and uploading your updated CV, and feel free to contact:
Audrey Poluakan, Recruitment Consultant at Grafton Netherlands
Email: audrey.poluakan@grafton.com
M: 0658069570
