C&Q Engineer (m/f/d)
Responsibilities
- GMP Biopharma experience in designing and execution of IQ/OQ/Qualifying/reQ protocols for Stainless Steel Media and/or Buffer tanks/vessels
- Design and execute CIP/SIP Qualification of SS vessels and transfer lines
- Requalification of current CIP/SIP processes, like reducing CIP/SIP cooldown time-lines
- Design and execute Room temperature mappin
- Experience with PCS/MES Siemens software
Profile
- Proven GMP Biopharma experience in Commissioning & Qualification
- Strong hands-on experience with CIP/SIP systems and stainless steel equipment
- Experience with PCS/MES Siemens systems
- Structured, detail-oriented, and documentation-driven mindset
- Very good English skills (German is advantageous)
Benefits
- Renowned pharmaceutical company
- Working in a major project
- Hays benefits
- Attractive Salary package
About Hays
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.
Staffing process for freelance specialists
- Analysis of qualifications
- Telephone or personal interview
- Contact with customers
- Contract with Hays
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1. Analysis of qualifications
We carry out a detailed analysis of your technical qualifications on the basis of your CV, your application documents and your profile.
Contact at Hays
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