Senior Scientist Raw Material (m/f/d)

With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.

• Ensure GMP-compliant introduction and release of manufacturing materials, including specifications, sampling plans, and documentation
• Review analytical data in LIMS, including job authorization, result certification, and ensuring data integrity
• Independently review and certify raw data, including internal and external Certificates of Analysis (CoA)
• Manage deviations, Out of Specification (OOS) results, and change controls within the area of responsibility
• Maintain audit and inspection readiness, including participation in customer and authority audits
• Collaborate with QA and Supply Chain to resolve quality issues related to material batch release
• Support creation of Material Qualification Forms and technical specifications in collaboration with process owners
• Participate in Gemba Walks and mock audits to drive continuous improvement
• Contribute to PPI projects and other QC processes as needed
• Act as a subject matter expert, leading or supporting resolution of technical issues

• Bachelor’s or Master’s degree in Life Sciences (e.g., chemistry, biochemistry, biology); alternatively, a laboratory apprenticeship with relevant industry experience may be accepted
• Solid experience in GMP-regulated industries, ideally within global corporate environments
• Hands-on experience in pharmaceutical Quality Control and/or Quality Assurance
• Proven experience managing deviations, change controls, and CAPA processes
• Strong collaboration skills with cross-functional teams to drive project success
• Fluency in English is required; German proficiency is a strong asset
• Experience with ERP systems, especially SAP, is advantageous
• In-depth understanding of GMP regulations and standards to ensure compliance
• Excellent technical writing skills for accurate documentation and reporting
• Ability to work independently and act as a subject matter expert in assigned areas

• Renowned pharmaceutical company
• Furhter paid training oppurtunities
• Attractive salary package

Ihr Kontakt

Referenznummer
836328/1

Kontakt aufnehmen
Telefon:+41 44 225 50 00
E-Mail: positionen@hays.ch

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