Validation Engineer / Validation Engineeress

Neocleus AG - June 14, 2025

Join SCHOTT Pharma as a (Senior) Validation Engineer

SCHOTT Pharma designs solutions grounded in science to ensure that medications are safe and easy to use for people around the world - because human health matters. Our portfolio features drug containment and delivery solutions for injectable medications, including prefillable glass and polymer syringes, cartridges, vials, and ampoules. Every day, our dedicated team of approximately 4,700 professionals from over 65 nations works tirelessly to contribute to global healthcare.

We are seeking a (Senior) Validation Engineer to join our R&D and Global Engineering division at our site in St. Gallen, Switzerland. As part of this role, you will engage in project-specific travel to our global production sites, which will be around 10% of your time.

Your Responsibilities

  • Develop and implement the qualification and validation strategy for local and global projects, providing consultation to the organization on qualification and validation topics.
  • Oversee the planning and execution of qualification and validation activities, including project management and coordination for global development and CAPEX projects.
  • Conduct and facilitate risk analyses (e.g., GMP-RA, FMEA) in accordance with specifications and industry standards.
  • Create, review, and update qualification and validation documents such as plans, test plans, protocols, and reports.
  • Proactively influence the continuous development of qualification and validation processes, thereby supporting the growth of SCHOTT Pharma.

Your Qualifications

  • University degree in engineering, computer science, life sciences, or a related field, including advanced training.
  • Over 3 years of practical work experience in qualification and/or validation within a regulated environment (experience in the pharmaceutical industry is preferred).
  • Strong understanding of GMP (Good Manufacturing Practice), data integrity, GAMP, 21 CFR Part 11, EU GMP Annex 11, and good documentation practices.
  • Excellent technical understanding and analytical skills; experience in technical writing is an advantage.
  • Intercultural openness, effective communication skills, and a structured, entrepreneurial approach to work.

Your Benefits

  • International assignments.
  • Flexible working hours.
  • Canteen services.
  • Access to public transportation.

Apply online using the form below. Please note that only applications matching the job profile will be considered.

Location : St. Gallen
Country : Switzerland

Application Form

Please enter your information in the following form and attach your resume (CV)

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