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Senior scientist, quality control

Eschborn
Terumo Deutschland GmbH
Scientist
Inserat online seit: 11 Juni
Beschreibung

MSAT Senior Scientist
The Manufacturing Science & Technology (MSAT) department in our Leverkusen site plays a central role in ensuring the technical success of drug product manufacturing. This team supports technology transfers, process validation, technology development, and troubleshooting across the Drug Product value chain. As MSAT Senior Scientist, you will be responsible for leading and supporting technology transfers, scale‑up activities, and process validation for drug product manufacturing, with a strong focus on Pre-Filled Syringes (PFS). You will act as a subject matter expert for drug product technologies, contribute to process and technology development, and support operational excellence across the site. The role combines strategic thinking with hands‑on involvement on the shopfloor, close client interaction, and cross-functional collaboration.
Lead and support process scale‑up, development, and optimization of drug product manufacturing processes, with a primary focus on PFS and full process chains including thawing, formulation, filling, and assembly/packaging.
Author and review technical documentation (protocols, reports, submissions) and provide scientific support during audits and client interactions.
Support new product introductions by leading risk assessments and defining the process control strategy, and contribute to late‑stage projects by preparing process descriptions, process instructions, and Bills of Materials (BOMs).
Demonstrate hands‑on engagement during tech transfer and manufacturing activities, while systematically sharing knowledge and contributing to team capability building.
Advanced degree (PhD or MS) in Biological Sciences, Engineering or a related field, with 3+ years (PhD) or 5+ years (MS) of pharmaceutical industry experience.
Over 3 years of project leadership experience, managing complex cGMP Drug Product manufacturing or development projects.
Proven ability to lead complex cross-functional projects involving multiple internal and external stakeholders.
Strong analytical and problem‑solving skills, with a data‑driven approach to troubleshooting and process improvement.
Hands-on, proactive mentality with the ability to work effectively on the shopfloor and support real‑time troubleshooting.
Ability to transfer knowledge effectively, contribute to team development, and support long-term MSAT strategy building.
Experience with project management tools and Minitab is an asset.
A meaningful impact on global healthcare: Contribute directly to the successful manufacturing of high‑quality drug products, supporting patients worldwide and shaping the future of our Leverkusen site’s technological capabilities.
Work in a setting where scientific excellence, data‑driven decision making, and continuous improvement are truly valued and embedded into daily operations.
Collaborate closely with Manufacturing, QA, Engineering, Development, and external partners, and represent MSAT during client interactions, audits, and project discussions.
Professional growth and development: Expand your expertise through hands‑on manufacturing exposure, advanced technology development projects, and opportunities to contribute to long-term strategy building. Training opportunities and development programs support your continued growth.
Competitive compensation and benefits: Receive a market‑competitive salary and benefits package aligned with your experience and impact, along with the stability and career opportunities of a global biopharmaceutical organization.

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