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Non-clinical Quality Assurance Leader
il y a 2 semaines
Non-Clinical Quality Assurance Leader:
Location
- Liege, Belgium
Business Sector
- Biotechnology
Job ref
- 23137
Published
- about 1 hour ago
Non-Clinical Quality Assurance Leader
Calling all talented professionals craving an exciting career move Here's your chance to join a thriving CROD in Liege, Belgium.
Key responsibilities:
- Contribute to meet GLP regulatory compliance for the Test Facility (OECD guidelines).
- Ensure implementation of processes and systems (e.g. facilities, equipment, personnel, methods, practices, records) according to the GLP nonclinical program of the Test Facility.
- Support the maintenance and continuous improvements of the QMS system.
- Prepare and/or review controlled documents (e.g., standard operating procedures, policies, CAPAs, change controls, master schedule).
- Review of study plans and study reports, amendments and deviations.
- Prepare the quality assurance program statement of the study plans and reports.
- Conduct facilityrelated, studyrelated and processrelated inspections to ensure compliance with applicable GLP regulatory requirements.
Key requirements:
- A master's degree in life sciences or closely related fields
- Prior experience in nonclinical quality assurance and GLP regulations (3+ years)
- Strong knowledge of GLP OECD guidelines
- Strong knowledge in nonclinical research
- Past experience in CRO is a plus
- Familiar with standard lab techniques (cell culture and molecular biology) is a plus
- Based in Belgium
Skills:
- Proficiency in both written and spoken English
- Excellent communication, organizational and scheduling skills, with ability to execute projects on time
- Solutionoriented way of working, problemsolving and analytical way of thinking
- Ability for rapid adaptation, proactivity and autonomy
- Team spirit and willingness to integrate a small structure where flexibility is a key factor.
Practicalities:
- Location: Liege, Belgium
- Startdate: ASAP
- Hybrid position
- Sound interesting?_
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