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Quality Control Compliance Supervisor
vor 3 Monaten
About NextPharma
NextPharma stands as a leading European contract manufacturer dedicated to the pharmaceutical, biotech, and healthcare sectors. Our workforce of 2,500 professionals is distributed across multiple European nations, all driven by a commitment to continuous improvement. We believe that passion is essential in delivering outstanding service worldwide.
Position Overview
We are currently seeking a Compliance Manager in Quality Control to enhance our operations.
Key Responsibilities:
- Support the management team in Quality Control operations
- Streamline processes within the Quality Control department
- Guarantee adherence to analytical standards in Quality Control, including pharmacopoeial monographs and test specifications
- Ensure that the internal quality management system complies with current GMP regulations
- Develop, update, and review Standard Operating Procedures (SOPs) and testing protocols focusing on GMP compliance
- Engage in the management of deviations and Out of Specification (OOS) results
- Contribute to the implementation of change control measures and Corrective and Preventive Actions (CAPA) in the Quality Control area
Additional Responsibilities:
- Examine analytical raw data and audit trails
- Plan and participate in the qualification of Quality Control equipment, including documentation preparation and review
- Develop or assess verification and validation plans
What We Provide:
- Tailored onboarding experience
- Flexible working arrangements, including remote work and 30 vacation days
- Company pension plan
- Employee engagement events and sports activities
- Training opportunities through our internal NextAcademy
- Career advancement possibilities across different sites
- Employee discounts
Candidate Requirements:
- Degree in natural sciences (Pharmacy, Chemistry, Biology, Biotechnology, or related fields)
- Extensive experience in pharmaceutical Quality Control and/or Quality Assurance
- Familiarity with relevant regulations, particularly EU GMP guidelines
- Open-minded, detail-oriented, and responsible work ethic
- Proficiency in Microsoft Office Suite
- Fluent in German and proficient in English, both written and spoken
