Do you thrive on shaping tomorrow’s biotech innovations? Do you feel energized by making a lasting impact in realizing life’s potential? If you’re ready to become the vital link between customer needs and successful equipment delivery, this role fits like a glove.
In this pivotal role, you'll:
Analyze customer process user requirement specifications for engineered biotech equipment—including technologies such as bioreactors, mixing systems, and storage vessels.
Lead projects as the technical point of contact from initial inquiry through final sign-off.
Provide expert technical support to our customers and sales teams across Cytiva’s Biotech product portfolio.
Position Objective:
As Project Manager, you will guide the technical scope of biotech equipment solutions for upstream processes. From process analysis and technology selection to commissioning and validation, you’ll ensure excellence across every step of execution. You’ll collaborate closely with internal teams and external partners to deliver customized solutions that meet the highest industry standards.
Key Responsibilities:
Lead customer engagement on process specifications and clarify technical requirements.
Take part in developing engineered equipment and Single-Use solutions, including detailed proposals and costing.
Manage project execution with a cross-functional team—establish timelines, coordinate resources, report progress, and maintain cost control.
Respond to RFIs and/or URSs and configure custom Single-Use system designs.
Coordinate and validate detailed mechanical, electrical, and functional designs.
Oversee creation and compliance of project documentation.
Plan and coordinate qualification activities, including pre-FAT and SAT testing.
Support customers during validation phases upon request.
Qualifications & Skills:
Bachelor's degree in Engineering, Biochemical, Process Engineering, Biotechnology, or equivalent experience. Master's degree preferred.
Initial experience with project/process engineering in biopharmaceutical manufacturing.
Proven ability to engineer biotech equipment in multicultural, multidisciplinary environments.
Familiarity with subcontractors across fabrication, software, electronics, and automation.
Hands-on experience with FAT/SAT qualification procedures in regulated biopharma settings.
Fluent in English. Knowledge of other European languages is a plus.
Ability to review and comment customer URS for Biotech equipment, and evaluate possible technologies or designs to meet customer requirements.
Knowledge and understanding of the current industry guidelines for designing, manufacturing, testing and documenting biopharmaceutical process equipment. (ASME BPE, GAMP, cGMP, ISPE, etc.)
Project management experience for the execution of system projects in accordance to the defined specifications, time schedule and cost.
Why Join Us?
At Cytiva, continuous improvement fuels everything we do. Learn how we work through theDanaher Business System. Join a global team of 63,000 committed individuals driven by purpose and powered by innovation. As a valued associate, you’ll try new things, receive meaningful guidance, and sharpen your skills while making real contributions.
We believe in belonging. We celebrate diverse perspectives and foster an inclusive culture where every voice matters—and every challenge is an opportunity to grow.
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.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.