Validation and Qualification Engineer (Worldwide) | ⚡⚡Validierungs- und Qualifizierungsingenieur (m/w/d) weltweit⚡
All-Jobs Personalservice GmbH
Job Summary
This role is for an experienced Validation and Qualification Engineer tasked with supporting high-profile clients within the GMP-regulated sectors, including Pharmaceuticals, Biotechnology, Life Sciences, and Medical Devices. The successful candidate will participate in quality assurance and GMP projects, focusing on the qualification of equipment and validation of processes according to the latest methodological and metrological standards. Key responsibilities include acting as a project coordinator or leader, conducting hygiene monitoring, and serving as a critical consultant for diverse quality assurance and GMP compliance inquiries. Applicants must possess an engineering degree in fields like Chemistry, Pharmaceutical Technology, or Biotechnology, coupled with specific experience in process validation for medical devices or pharmaceuticals. The position requires excellent German and English language skills, proficiency in SAP and MS Office, and a significant willingness to travel (40%) to client sites.
Required Skills
Education
Completed engineering degree (Master, Bachelor, Doctorate) in Chemistry, Pharmaceutical Technology, Biotechnology, Process Engineering, or a comparable natural science discipline.
Experience
- Experience with process validations in medical devices, biological products, or pharmaceuticals
- Professional experience in a GMP-regulated environment (Pharma, Biotechnology, Life Sciences, Medical Devices, Chemistry)
- Experience acting as a project coordinator or leader
Languages
Additional
- Willingness to travel (40%) to client locations.
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