Senior Scientist Bioreactor Process Design (all genders)

Evote; Toulouse; Sur place; EUR 50 000 - 80 000; Plein temps

Résumé du poste

Evote in Toulouse is seeking a Senior Scientist in Bioreactor Process Design to lead impactful projects in biotherapeutics manufacturing. The ideal candidate will have extensive experience in bioreactor cell culture, process design, and be proficient in English. Responsibilities include driving tech transfer, preparing bench-scale bioreactors, and serving as a technical resource for cGMP processes. This role promises opportunities for collaboration and innovation within a diverse and inclusive team environment.

Qualifications

• 8+ years of experience with a Master's or 6+ years with a Ph.D. in relevant fields.
• Experience in Biosimilar development and commercial process development.
• Expert in bioreactor technology, design of experiments (DOE), and statistical analysis.

Responsabilités

• Drive development and tech transfer for biotherapeutics manufacturing.
• Prepare and run bench-scale bioreactors and related equipment.
• Serve as technical resource for cGMP manufacturing and process design.

Connaissances

Bioreactor cell culture

Process Design

Statistical analysis (DOE)

English proficiency

Formation

Master’s or Ph.D. in Engineering, Biochemistry, Biology or related field

Outils

JMP

R

Python

Description du poste

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!

Location: Toulouse, France.

Type of contract: Permanent

We’re looking for a passionate and curious Senior Scientist Bioreactor Process Design to join our team.

If you’re excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit.

In this role, you’ll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories.

You’ll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. It’s a role where your curiosity will fuel both your personal growth and the success of the team.

What You’ll Do:

• Driving development and tech transfer of early and late‑stage (characterization and validation) upstream perfusion/intensified fed‑batch processes for biotherapeutics manufacturing as well as technology development projects.
• Prepare and run bench‑scale bioreactors and bioreactor‑related equipment (controllers, pumps, autoclaves, etc.).
• This may include but not limited to, build and autoclave bioreactor parts and assemblies as well as assisting with bench‑scale bioreactor operations (daily sampling and analytics, inoculation activities, run preparation, and troubleshooting).
• Serve as a functional area lead for Biosimilar early and late‑stage Process Characterization (PC) projects as well as technology development projects.
• Serve as an internal technical resource for cGMP manufacturing and Process Design, as well as a resource and subject matter expert for external clients and partners for cell culture and bioreactor processes (small‑scale models, process transfer, and scale up).
• Communicate experimental plans and data to teams and clients clearly and effectively, including communicating scientific information to a diverse set of audiences, including external clients, vendors, and technology development collaborators.
• Independently design, execute, and analyze statistically designed experiments (DOE).
• Author SOPs, reports, and slides which summarize, organize, and interpret experiment results with review by appropriate team members.
• Train and mentor junior staff and interns within a matrix reporting structure.
• Potential for weekend work and being on‑call for critical bioreactor runs. All different missions.

Who You Are:

• Master’s in engineering, Biochemistry, Biology, or related field with 8+ years of experience or Ph.D. in Engineering, Biochemistry, Biology, or related field with 6+ years of experience.
• Proficiency in both verbal and written English is essential.
• Expert in bioreactor cell culture and perfusion technology development and tech as well as CMC sections authoring regulatory filings.
• Experience in Biosimilar development.
• Experience with commercial process development, process characterization, and validation.
• Expertise in design of experiments (DOE) and statistical analysis.
• Experience with high throughput cell culture (e.g., HT assays, robotics such as Ambr systems, lab automation, or multi‑omic data) is a plus.

Pluses

• Experience analyzing data in tools such as JMP, R, or Python.
• General understanding of cell biology, fluid dynamics, and biotransport as well as knowledge in other functional areas (downstream purification and analytical sciences).
• General understanding of circuits (grounding, power, signal, etc.).
• Experience working in a cGMP or clean room setting (this job is non‑GMP but knowledge of GMP is helpful for process/tech transfer activities).

ENG : In the frame of our Diversity policy, Evotec considers, with equal competences, all applications including people with disabilities.

FR : Dans le cadre de sa politique Diversité, Evotec étudie, à compétences égales, toutes les candidatures dont celles des personnes en situation de handicap.