Quality Assurance Specialist
vor 4 Wochen
In this role, you will play a critical part in ensuring the quality and integrity of our clinical drugs. Your daily tasks will include reviewing and releasing incoming label stock, clinical finished goods, and batch records. You will also collaborate closely with internal functional areas and external partners to ensure timely supply of clinical drugs to patients.
Key Responsibilities:- Review and release of incoming label stock and clinical finished goods
- Review of batch records and regulatory filings
- Collaboration with internal functional areas and external partners
- Communication of batch-related issues to management and regulatory authorities
- Bachelor's or Master's Degree in life sciences, ideally in biotechnology, biology, or pharmaceutical studies
- Minimum of 2 years' experience in the good manufacturing environment within the pharmaceutical business or comparable
- Experience in batch record review and Good Documentation Practices
- Excellent problem-solving skills, preferably with Six Sigma Tools
- Proficiency in English and German language, with business-level proficiency required
As a Quality Assurance Specialist, you will have the opportunity to work in an international leading company and drive issue resolution. You will be part of a dynamic team and have the chance to develop your skills and expertise in quality assurance. If you are a motivated and detail-oriented individual with excellent communication and writing skills, we encourage you to apply for this exciting opportunity.
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