Product Expert / Analytical Process Manager (m / f / d) - 2 year contract

Advancing medicine to save lives. Together.

Thanks to many decades of experience and our passion for what we do, we make an essential contribution to the global availability of biopharmaceuticals, especially for patients with rare and serious diseases.

Rentschler Biopharma SE is a leading contract development and manufacturing organization (CDMO) focused exclusively on client projects. We offer customized full-service solutions for bioprocess development and the production of complex biopharmaceuticals. As a German family-owned company with an international footprint and global reach, we combine experts, expertise and years of experience to develop best-in-class solutions – together with our clients.

Rentschler Biopharma has approximately 1,400 employees and is headquartered in Laupheim, Germany, with a site in Milford, MA, USA. In 2024, we joined the United Nations Global Compact, underlining our commitment to sustainability.

As an independent family-owned company, we live by the motto : Many hands, many minds - ONE TEAM! Open, respectful cooperation characterizes our working environment, where quality awareness, diligence and responsibility are our top priorities. With all the diversity of our talents in the Rentschler team, we pursue one vision together : advancing medicine to save lives.

As Product Expert / Analytical Process Manager you are responsible for the implementation of the Quality-by-Design (QbD) concept as well as all activities of the Analytical Science group in customer projects.

Tasks and responsibilities

• Representation of Analytical Science in the customer project teams
• Coordination of activities of Analytical Science for the assigned customer projects including external biophysical analytical activities
• Scientific contributions and coordination of Critical Quality Attributes (CQA) evaluations and product characterization studies
• Implementation of the QbD strategy in the respective customer project teams
• Advise teams and clients on strategic decisions regarding cQAs and QbD based development of biopharmaceuticals
• Responsibility for adhering to timelines and milestones according to the overall project plan
• Contribution to risk assessments regarding product quality
• Preparing and writing reports and presentations in English language
• Presentation of results and strategic topics in internal meetings, customer meetings, audits and scientific conferences

What is important to us

What you can look forward to