GMP Compliance Expert
6 days ago
About the Role:
We are seeking an experienced Quality Assurance Specialist to join our team in Copenhagen. As the ideal candidate, you will possess a strong background in quality management and a deep understanding of Good Manufacturing Practice (GMP) principles.
The role is critical in ensuring that our production facilities and laboratories comply with current GMP standards, including EU GMP, 21 CFR, and ICH guidelines at all times.
Key Responsibilities:
- Quality Assurance Review: Oversee the review and approval of technical documents, including change controls, deviations, CAPAs, risk assessments, SOPs, validation plans, requirements specifications, qualification protocols, and reports.
- GEMBA Walks: Conduct regular GEMBA walks in GMP areas to ensure adherence to quality standards.
- Communication: Maintain open communication with internal and external stakeholders to resolve issues and clarify points of concern.
- SOP Development: Contribute to the development of standard operating procedures (SOPs) for qualification, calibration, maintenance, cleaning, and other facility and engineering activities.
Requirements:
- A science-based degree.
- Experience working in or directly supporting manufacturing operations in a drug substance/product manufacturing site.
- Prior biopharmaceutical experience is desirable.
- A thorough understanding of GMP principles and guidelines.
- Experience with the qualification of GMP facilities, equipment, and computerized systems.
- Knowledge of Data Integrity principles.
- Strong decision-making skills and a proactive attitude.
- Excellent written and verbal communication skills.
- Ability to work efficiently in a fast-paced, matrix environment.
- Ability to meet deadlines and effectively manage multiple tasks.
- Flexibility to adapt to changing business needs and priorities.
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