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Open nowPosted 26 hours ago

Senior QC Systems Specialist

EURES job mobility portal576,476 open roles

Where
Groot-Amsterdam, Netherlands
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Your applicationOpen nowSenior QC Systems SpecialistEURES job mobility portal · Groot-Amsterdam, Netherlands

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The clock on this job

Early applications get read.

10.5% of postings close within 7 days. Measured by our own scanner across the market. EURES job mobility portal postings stay open a median of 9 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.3%3 days
  3. 10.5%7 days
  4. 15.9%14 days
  5. 34.1%30 days
This job: posted 26 hours ago

EURES job mobility portal median: 9 days open

The posting

Bewaar Senior QC Systems Specialist QC Systems Specialist I Amsterdam | QC Systems Specialist | GMP As Senior Specialist I - Quality Systems, you will support the deployment, governance, maintenance, and continuous improvement of Kite Pharma's Quality Management System. Acting as a compliance partner across multiple departments and stakeholders, you will ensure site quality systems remain compliant with GMP regulations, regulatory requirements, and Kite quality standards. Key Responsibilities - Manage and maintain Quality Systems including Change Control, Deviation, CAPA, and Material Review Board (MRB) processes. - Deliver Quality Systems training and support user adoption across the site. - Act as backup chair for the Change Control Review Board, Deviation Board, and Material Review Board. - Monitor site compliance through metrics, governance activities, and management reporting. - Review and approve changes, deviations, CAPAs, and quality system documentation. - Support regulatory inspections, internal audits, and quality system assessments. - Ensure proper maintenance of cGMP documentation and Quality Management System records. - Identify and mitigate quality risks in accordance with regulatory guidelines and company procedures. - Lead or support cross-functional quality initiatives and site start-up activities. - Drive continuous improvement projects within Quality Systems processes. - Support automated reporting tools and workflows when required. - Provide day-to-day guidance to team members and act as backup to the Senior Manager Quality Systems. What you'll need to succeed The successful candidate will hold a degree in Life Sciences, Bio‑Engineering, or a related field, with a background in GMP‑regulated QC laboratory work. Key requirements include: - Strong knowledge of GMPs, pharmaceutical Law and legislation - Experience with Change Control, CAPA, Internal Audit, Deviations, MRB and other ICHQ10 quality system...

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