Downstream Processing Scientist

Rentschler Biopharma is a leading global contract development and manufacturing organization (CDMO) for biopharmaceuticals. From our headquarters in Laupheim, Germany, and our site in Milford, MA, USA, we offer end-to-end solutions, including bioprocess development and manufacturing, as well as related consulting activities such as project management and regulatory support. In Stevenage, UK, we have launched Rentschler ATMP Ltd. dedicated to cell and gene therapies.

We are a family-owned company with approximately 1.400 employees from 25 nationalities. What unites us at Rentschler Biopharma, is the passion for what we do. We empower our clients to help patients with serious or rare diseases. With our dedication and expertise, we convert medical research into outstanding biopharmaceuticals. Thus, we provide an important contribution to the global availability of essential therapies. Going forward, we are expanding our team to ensure our long-term sustainable growth. Join us and be part of a unique journey, shaping the future of biopharmaceutical manufacturing together!

Tasks and Responsibilities:

Support establishment and expansion of the Gene Therapy Process Development Capabilities at Rentschler ATMP.

Coordinate/plan/execute the delivery of downstream process development programs for customer gene therapy products.

Perform end to end DSP development activities from lab to pilot scale (Buffer Preparations, Filtration, Chromatography, TFF….) under line manager / client requirements.

Writing / adapting all relevant DSP documents (e.g. process descriptions, protocols, reports).

Completing technical transfers from clients to PD and further into GMP.

Provide technical and project specific support to address customer queries and project updates.

Identify and escalate issues as they occur, troubleshoot issues through technical expertise, and report accordingly with all relevant information.

Act as a DSP equipment owner, troubleshoot issues, and ensure equipment is serviced and fully operational in support of lab management activities.

Support GMP operations and other departmental functions (procurement, commissioning, qualification, validation and safety) as required.

What is important to us:

Degree in Life Sciences or Biological / Chemical / Biochemical Engineering or higher qualification

Industry experience with relevant biopharmaceuticals roles within the area of DSP (1-4 years depending on qualification and experience).

Technical and practical understanding of DSP unit operations (filtration, chromatography and TFF) and their optimisation and scaling.

Awareness of viral vector bioprocessing challenges, current state of art, and future industrial trends.

Experience of lab to pilot scale bioprocessing equipment, including single use equipment, and their consumables.

Capable of experiment execution, reporting, and design.

Awareness of industry GMP manufacturing standards for GMP compliant scalable processes.

Good organisational and communication skills, experienced in liaising with internal and external stakeholders providing a credible interface as a technical SME.

Team player able to energise and motivate the team.

What We Offer:

Employment in a company that offers real added value and manufactures medicines for seriously ill patients.

To be part of the ATMP growth and success story, participating in the development of a great company culture based on teamwork, empowerment and opportunity for personal growth.

A holiday entitlement of 28 days plus public holidays.

Flexible working conditions

An above market pension provision increasing with length of service.

Private medical health care and benefits scheme.

Plus other additional benefits.

JR1601