Process Validation Engineer
Listed on 2026-11-04
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Engineering
Validation Engineer, Process Engineer, Biomedical Engineer, Pharma Engineer
Founded in 1968,
SKAN is a pioneer in cleanroom equipment and the development of isolators for the pharmaceutical industry. Innovative products, tailor-made solutions and an effective service organization have made SKAN a market leader and a key partner to industry and research laboratories.
We are looking for a motivated Process Validation Engineer (PVE) for the Process Validation Microbiology (PVM) department. The PVM team consists of professionals with a wide range of cultural, academic and professional backgrounds. Our team specialises in the development and validation of decontamination processes (H2O2 and E-Beam) for pharmaceutical isolators, which are a key element in the aseptic manufacturing of sterile drugs.
As a member of this team, you will have the opportunity to travel worldwide to support our pharmaceutical customers in their life-saving projects. This role therefore involves up to 50% international travel to our customers.
- Development, validation and implementation of decontamination processes
- Creation of test protocols and test reports
- Enabling customer-orientated decontamination processes with maximum safety and efficiency
- Process optimisation and requalification of existing processes as well as customer-oriented troubleshooting and consulting
- Carrying out internal and external training for customers
- Supporting cross-functional technological improvements and innovations
- Assisting with the maintenance, updating and improvement of internal SOPs, documentation and workflows
- A university degree (Bachelor's or Master's) in life sciences, engineering or technology is required
- Experience in one of the sterilisation technologies (steam, irradiation or ETO) and/or isolator decontamination (H2O2 and/or e-beam) is very welcome
- Experience in cleanroom qualification in the medical device and/or pharmaceutical industry is also appreciated
- Experience in process validation (IQ/OQ/PQ) is an advantage
- Very good knowledge of English is required, any other foreign language is a plus
- You have a professional, reliable way of working, especially for customer contact (internal and external) and can take on personal responsibility
- Furthermore you are a motivated person who likes to work carefully and in compliance with GMP
- You are comfortable dealing with different cultures and enjoy working with others in a collegial and team-orientated manner
- You are flexible, especially beacause of the fact that assignments cannot always be planned far in advance
- An open and collaborative corporate culture
- Freedom to contribute and develop ideas
- Opportunities to participate in sports and social activities
- Professional development and continuous learning opportunities, especially at our SKAN Academy
- Comprehensive and career-focused onboarding
- Quick decision-making paths and flat hierarchies
- Transparent and open communication
- 5 weeks of vacation, with the option to take additional leave
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