Synthesize and optimize biologics manufacturing processes to ensure efficient production.
Key Responsibilities
* Contribute to feasibility studies in capital investment projects, assessing process design and evaluating manufacturing units.
* Evaluate and assess the design of manufacturing units for biologics production.
* Deliver all inputs required for suite and equipment design, commissioning, and qualification phases.
* Develop GMP documents for relevant areas, ensuring compliance with regulations.
* Lead project execution, prioritizing quality, time, and cost factors from a MSAT perspective.
Requirements:
* A Master's or Ph.D. degree in bioconjugation, biotechnology, chemical engineering, organic chemistry, or related fields.
* Over five years of experience in biopharma manufacturing, preferably in bioconjugates or downstream processing (DSP).
* Familiarity with CAPEX project handling.
* Excellent communication skills for customer interaction and collaboration within project teams.
* Proficiency in English; knowledge of German is an asset.
* Creative, agile, and open-minded individuals who thrive in dynamic environments.
About the Role
This role offers an exciting opportunity to contribute to the growth and development of biologics manufacturing processes. If you are passionate about driving innovation and excellence in a collaborative environment, we encourage you to apply.