Validation Engineer (m/f/d)

Validation Engineer (M/W/D)

Bring more to life.

Are you ready to unfold your potential and make a real impact in the fields of life sciences, diagnostics, and biotechnology?

At Cytiva, one of more than 15 operating companies of Danaher, we save lives – and we are all united by a commitment to innovations that make a tangible difference.

You will thrive in a culture of belonging where you and your unique perspective matter. And by leveraging Danaher’s system of continuous improvement, you will help turn ideas into action – with innovations in real time.

Working at Cytiva means developing new solutions to improve human health at the forefront. Our amazing customers conduct life-saving activities ranging from fundamental biological research to the development of innovative vaccines, new drugs, and cell and gene therapies.

At Cytiva, you can continuously improve yourself and us by working on truly important challenges with people who care about each other, our customers, and their patients. Take the next step in a career that will change your life.

Learn more about the Danaher Business System that makes all this possible.

At our production site in Pasching with about 260 employees, we produce cell culture media in liquid and powdered form for the biopharmaceutical industry.

To strengthen our engineering team at the Pasching site, we are looking for a Validation Engineer (m/w/d) to join us on a temporary basis for 12 months. In this role, you will support us in the acquisition and commissioning of production facilities as well as in the optimization and validation of production processes. You will be part of a 4-person team and report to the engineering team leader of liquid production.

What you will do:

• Planning, conducting, and coordinating routine validations as well as temperature mappings in the production area
• Creating validation protocols and reports (e.g., cleaning, mixing, filling, sterilization, transport)
• Independently preparing and handling validations, feasibility studies, and risk analyses
• Supporting qualification activities and creating SOPs in compliance with GMP guidelines as well as participating in customer audits

Who you are:

• Completed education in biotechnology, food technology, environmental engineering, medical technology, or similar fields
• Experience in the field of qualification, validation, laboratory practice, or quality management in the pharmaceutical industry is desirable
• Advanced MS-Office skills as well as very good German and English language skills
• Team capability, networked thinking, and independent working style

What we offer:

• We bring meaning and challenge to everyday work
• Numerous benefits (e.g., public transport ticket, meal and fitness cost subsidy, employee assistance program, bonuses)
• Good public accessibility or parking spaces
• A collegial and appreciative climate as well as an international company environment in a rapidly growing industry
• Flexible working hours and opportunities for professional development

The minimum salary for this position is € 47,500 EUR gross per year (full-time), the actual salary is dependent on qualification and professional experience.

Become part of our successful team today. Together, we accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.