Validation Engineer (m/w/d)

About Us

Bring more to life. Are you ready to unleash your potential and make a real difference in life sciences, diagnostics, and biotech. At Cytiva, one of Danaher’s more than 15 operating companies, we save lives – and all of us are united by a common commitment to innovations that have a tangible impact. You will thrive in a culture of belonging where you and your unique perspective count. And by leveraging Danaher’s continuous improvement system, you’ll help turn ideas into impact – with real-time innovation. Working at Cytiva means developing new solutions at the forefront to improve human health. Our great 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 towards a career that will change your life. Learn more about the Danaher Business System that makes it all possible.

At our production site in Pasching with approx. 260 employees, we produce cell culture media in liquid and powder form for the biopharmaceutical industry. To strengthen our Engineering team at the Pasching site, we are looking for a Validation Engineer (m/f/d) for the earliest possible start date, for a limited period of 12 months. In this role, you will support us with the procurement and commissioning of production facilities as well as with the optimization and validation of production processes. You are part of a 4-person team and report to the Engineering Team Leader of Liquid Production.

What you'll do

• Planning, execution, and coordination of routine validations as well as temperature mappings in the production area
• Creation of validation protocols and reports (e.g. cleaning, mixing, filling, sterilization, transport)
• Independent preparation and execution of validations, feasibility studies, and risk analyses
• Support with qualification activities and creation of SOPs in compliance with GMP guidelines, as well as participation in customer audits

Who you are

• Completed training in biotechnology, food technology, environmental technology, 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 and very good German and English language skills
• Teamwork, networked thinking, and independent working style

What we offer

• We bring meaning and challenge to daily work
• Numerous benefits (such as public transport ticket, food and fitness subsidies, Employee Assistance Program, bonuses)
• Good public accessibility or parking spaces
• Collegial and appreciative atmosphere as well as an international corporate 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 depends on qualifications and professional experience.

Join Us

Become part of our successful team today. Together, we’ll 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. For more information, visit .

Join our winning team today. Together, we’ll 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.