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QA specialist - CAPA/Deviation's
Job
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!
