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QA specialist - CAPA/Deviation's

  • Locatie:

    Leiden, Nederland

  • Contactpersoon:

    Douwe Wieringa

  • Contractsoorten:

    Permanent

  • Telefoon contactpersoon:

    +31 (0)20 406 97 50

  • Bedrijfssectoren:

    Pharmaceutical , Biotechnology

  • E-mail contactpersoon:

    douwe_wieringa@oxfordcorp.com

Would you like to work for an innovative company in the biotechnology sector? In this position, you can contribute to pioneering cell therapy for cancer patients. As a GMP Specialist, you will have a crucial role in ensuring quality and efficiency. Interested? - Read on quickly!
Job Description
As a GMP Specialist, you will strengthen the Manufacturing team and support GMP activities around equipment and systems across multiple locations. You are an ambassador for the overall GMP culture and a hands-on expert in handling deviations, CAPAs and continuous improvement projects.

Responsibilities

* Improve GMP awareness within the organization
* Supervise colleagues in handling deviations and CAPAs
* Monitor the progress of deviations and CAPAs
* Oversee training assignments within the department
* Support root-cause investigations and implementation of change controls
* Drive a culture of continuous improvement
* Work closely with Quality Assurance and other departments

Profile

* BSc/MSc in life sciences, biotechnology or engineering
* At least 3 years of experience within a pharmaceutical or biotech company as a process engineer
* Experience with quality record management, Root Cause Investigation and CAPA
* Eye for detail and experience in a GMP environment
* High sense of responsibility
* Fluent command of the English language


Terms of employment

* Contract: Initially 6 months via secondment. with realistic long term perspective
* Salary indication: €2800 - 5700, depending on your experience
* Working hours: 40 hours per week
* Region: Leiden
* Job number: 24961


Interested? Apply now and contribute to the future of cancer treatment!