Quality Assurance Specialist
ClinChoice(1 month ago)
About this role
ClinChoice is hiring a Quality Assurance Specialist to work onsite in Groningen (4 days/week) on a client-dedicated assignment through December 2026. The role is client-facing and embedded with a large pharmaceutical/biomedicines partner, providing quality oversight, ensuring regulatory compliance and supporting cross-functional projects. The position offers opportunities to work on validation, R&D and engineering projects while representing the CRO to the sponsor.
Required Skills
- Change Control
- Document Control
- Compliance
- Procedure Writing
- Trend Analysis
- Nonconformity Management
- CAPA
- QMS
- Continuous Improvement
- Validation Planning
+8 more
Qualifications
- Bachelor's Degree or Equivalent
- 4-6 Years Experience
- Medtech/Pharma Experience
- Validation Experience
- Knowledge of GMP
- Knowledge of MDD/MDR
- Knowledge of QSR CFR 820
- Knowledge of ISO 13485
- Knowledge of ISO 14971
About ClinChoice
clinchoice.comClinChoice is a full‑service global contract research organization (CRO) that helps accelerate drug and medical device approvals to market. They offer end‑to‑end clinical development, regulatory strategy, and operational support across study design, execution, data management and safety to guide sponsors through all phases of development. With global site networks, therapeutic expertise and data‑driven processes, ClinChoice aims to shorten timelines and reduce risk for development programs. They partner with biotech, pharma and device companies to navigate complex regulatory pathways and bring safer products to patients.
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