Process Engineer Downstream - Fixed Term (all genders)

We’re excited to share this opportunity as 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.

Location: Toulouse, France.Type of contract: Fixed Term 4 monthsStart date: immediately

What You’ll Do

As part of the project to build a biopharmaceutical manufacturing facility, you support Manufacturing Operations, bringing expertise in process control and equipment management.

You act as equipment owner for manufacturing, ensuring life cycle management of equipment you are in charge of.

Support Investigation and CAPA for process related topics in production.

Support CQV activities (IOQ and PQ) bringing technical expertise on DSP process.

In charge of supporting manufacturing in case of troubleshooting and improvement projects.

In charge of manufacturing equipment maintenance plan definition and good execution in alignment with Maintenance planner.

Support creation and review of technical documentation associated to manufacturing process such as SOP, Work Procedures, and batch reports.

Who You Are

• Bachelor’s degree in engineering science or related program with 3+ years of relevant experience.
• Verbal and written communications skills in both English and French.
• Understanding bioreactors, chromatography, and filtration processing equipment and operations used to manufacture biotherapeutics.
• Experience with equipment commissioning, qualification, and validation activities.
• Proven knowledge of cGMP requirements; commercial site experience is a plus.
• Technical support and troubleshooting for critical manufacturing operations during Engineering and GMP processing.
• Hands‑on experience with single use flow path operations and disposable‑based manufacturing technologies, from bench to commercial scale.
• Operation in process control systems and development of automation recipes.
• Ability to organize, analyze/interpret, and effectively communicate data.
• Authoring technical and quality documentation within GMP systems.
• Execute process and equipment risk assessments using industry‑standard tools (e.g. FMEA).
• Good interpersonal, team, and collaborative skills are a must.
• Excellent oral and written communication skills.

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.

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