Pharmaceutical Audit Specialist
vor 2 Monaten
We are seeking a highly skilled Audit Manager to join our team at Siegfried. As a key member of our quality assurance team, you will be responsible for planning and conducting audits of contract manufacturers, contract laboratories, and other service providers.
Key Responsibilities- Plan and conduct audits to ensure compliance with regulatory requirements and company standards
- Qualify suppliers and evaluate audit results to identify areas for improvement
- Collaborate with cross-functional teams to develop and implement quality management systems
- Conduct internal audits and provide recommendations for process improvements
- Respond to customer inquiries and provide quality-related information
- Completed scientific studies (ideally with a doctorate)
- At least 3 years of professional experience as an auditor in a chemical, pharmaceutical, or similar environment
- Comprehensive expertise in quality management, particularly with regard to ISO and GMP
- Knowledge of cGMP, preferably in the production of active ingredients and/or finished medicinal products
- Business fluent in German and English
- Flexible and familiar with working in a matrix organization
- Flexible working hours to balance work and personal life
- Discounts on health insurance and supplementary insurance
- Generous share purchase plan and customizable benefits
- Family allowance and child allowance
- Individual further training opportunities
- Reka money and pension fund contributions
- Catering at preferential conditions and free credit card
Siegfried is a leading Custom Development and Manufacturing Organization (CDMO) with a global presence. We develop and produce active pharmaceutical ingredients (API), intermediates, and finished dosage forms. Our comprehensive services range from early-stage Research & Development to commercial production. We are committed to providing a flexible, diverse, and discrimination-free working environment where employees can develop personally and professionally.
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