Scientist, Drug Product Development (all genders)

Job Title: Scientist, Drug Product Development

Location: Toulouse
Department: Process & Product Design
Reports To: Senior Manager, Drug Product Development

We’re excited to share this opportunity is part of the Sandoz acquisition of Just-Evotec Biologics in Toulouse. Through this opportunity you will impact the lives of hundreds of millions of people through bold ideas supported by an inclusive, agile company culture. Join us to help make healthcare fairer and faster, help us to pioneer access to medicine! Click to learn more.

What You’ll Do:

• ·Design and execute phase-appropriate formulation, drug product process development and stability studies.

• Implement pharmaceutical product development strategy and conduct formulation development and PD process experiments.

• Represent the Drug Product Development function and work collaboratively with cross-functional P&PD teams to achieve organizational goals.

• Work with external CMOs for outsourced activities, including pharmaceutical manufacturing.

• Execute development strategies to increase efficiency and reduce risk of FIH, NIF and commercial formulations.

• Optimize development strategies for biosimilar formulations, considering intellectual property challenges.

• Act as a team member and collaborate with Just organization partner groups, including analytical, quality control, quality assurance and manufacturing teams, to ensure product quality and stability.

• Act as an internal technical resource for Quality, Manufacturing and Process Design, as well as a resource and subject matter expert for external clients and collaborators

• Be a technical resource to internal and external teams regarding formulation, stability and container closure for designing drug product

Who You Are:

• Holder of a Master’s degree in biotechnology, bioprocess engineering, pharmaceutical sciences, biochemistry or related filed with 0 to 5 years of relevant experience

• Knowledgeable and experienced with Biologics/Protein/peptide formulation and DP process development (mandatory)

• Able to prove practical hands-on experience of analytical techniques including HPLC/UPLC, Capillary Electrophoresis (CE), Isoelectric Focussing (IEF), Sub-visible particle analysis/characterization, DLS, DSC etc.

• Knowledgeable on design experiments (DoE) tools such as JMP, MODDE etc. and statistical analysis for biologic and/or biosimilar products.

• Comfortable with deep understanding of protein degradation and stabilization mechanisms

• Experienced in Drug product development and/or manufacturing of sterile injectable dosage forms including frozen, liquid, formulations in vials, pre-filled syringes and autoinjectors (will be preferred).

• Knowledgeable of regulatory guidance from the FDA and EMA for development of biologic drug products and biosimilars

• Knowledgeable of USP and Ph. Eur. as it relates to biologics development

• Language : very comfortable in English, including the ability to communicate effectively over teleconference and web-based meetings. At ease in French would be an added advantage

• Dynamic, having good interpersonal skills and being a team player 

• Having a comprehensive written and verbal French communication skills will be an added advantage

Why Sandoz?

Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, provided more than 900 million patient treatments across 100+ countries in 2024 and while we are proud of this achievement, we hav