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Process Engineer - Sterile Manufacturing

Job in 8400, Winterthur, Kanton Zürich, Switzerland
Listing for: Ophtapharm, a Sentiss Company
Full Time position
Listed on 2026-10-14
Job specializations:
  • Manufacturing / Production
    Validation Engineer, Pharmaceutical Manufacturing
  • Engineering
    Validation Engineer
Salary/Wage Range or Industry Benchmark: 90000 - 130000 CHF Yearly CHF 90000.00 130000.00 YEAR
Job Description & How to Apply Below

At Ophtapharm AG, we manufacture sterile ophthalmic medicines that help patients worldwide protect and improve their vision. As an FDA and EU-GMP certified pharmaceutical company, we combine the highest quality standards with entrepreneurial thinking, short decision-making paths and a clear focus on the future.

As our sterile manufacturing operations continue to evolve, we are investing in the people, processes and technologies that will shape our future. As part of the Engineering team, you will actively contribute to this transformation, bringing forward new ideas and helping to continuously improve processes, technologies and organizational structures. This is an opportunity to make a visible impact and shape the future of our company.

Your

Role
  • Develop and optimize manufacturing processes to sustainably improve quality, efficiency and process reliability.
  • Drive technical changes, continuous improvement initiatives and investment projects from concept through implementation.
  • Work closely with Production and Quality Assurance to solve challenges and establish sustainable solutions.
  • Enhance the reliability and performance of our sterile manufacturing processes while improving equipment and system availability.
  • Actively contribute to the further development of our manufacturing operations and make a direct impact on business success.
Your Profile
  • University degree in Chemical Engineering, Pharmaceutical Engineering, Process Engineering or a related technical discipline.
  • Experience in a pharmaceutical manufacturing environment, ideally within sterile manufacturing.
  • Sound knowledge of GMP requirements and their practical application.
  • Experience managing technical projects; exposure to qualification and validation activities is an advantage.
  • Very good German and good English language skills.
What you can expect
  • A key role with significant influence on the future direction of our manufacturing operations.
  • The opportunity to visibly drive technical innovation and change.
  • Short decision-making paths and an environment where ideas can be turned into action quickly.
  • Collaboration within an engaged team that values ownership and direct contribution.
  • Attractive employment conditions within an internationally active Swiss pharmaceutical company.
For recruitment agencies

Thank you for your interest. We are not engaging external recruitment partners for this position.

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