Process Engineer MSAT (all genders)

Evote; Toulouse; Sur place; EUR 55 000 - 75 000; Plein temps

Résumé du poste

Evotec in Toulouse, France, is seeking a Manufacturing Equipment Specialist to support operations and the lifecycle of manufacturing equipment. The role covers CQV activities, CAPA handling, and collaboration with maintenance planning to ensure reliable maintenance execution.

You will contribute to GMP documentation, SOP authoring, and resolution of equipment issues, from bench to commercial scale, while coordinating with cross-functional teams in English and French.

Qualifications

• Master or Engineer degree in engineering/biotech or related field.
• 3+ years of relevant experience in a similar role.
• Fluent in English and French (verbal and written).
• Knowledge of processing equipment and biotherapeutics manufacturing.
• Experience with equipment commissioning, qualification, and validation.
• Knowledge of cGMP requirements; commercial site experience is a plus.
• Technical support and troubleshooting for critical manufacturing operations.
• Hands-on experience with single-use flow path operations and disposable-based manufacturing.
• Operation of process control systems and development of automation recipes.
• Ability to organize, analyze/interpret and communicate data.
• Authoring GMP-compliant technical and quality documentation.
• Execute risk assessments using tools like FMEA.

Responsabilités

• Support Manufacturing Operations within a biopharmaceutical facility, applying expertise in process control and equipment management.
• Act as equipment owner for manufacturing, ensuring lifecycle management of equipment.
• Support investigations, CAPA and changes for process equipment topics.
• Support CQV activities (IOQ and PQ) with technical expertise on USP/DSP processes.
• Assist manufacturing in troubleshooting and improvement projects.
• Define and execute manufacturing equipment maintenance plans in alignment with Maintenance planners.
• Create and review technical documentation for manufacturing processes (SOPs, work procedures, batch reports).

Connaissances

Process control

Equipment management

CAPA/Changes

CQV support

Troubleshooting

Maintenance planning

Documentation GMP

cGMP knowledge

Single-use systems

Automation recipes

Data analysis

English & French bilingual

Formation

Master or Engineer degree in engineering/biotech

Description du poste

Location: Toulouse, France

Type of contract: Permanent

Start date: September 2026

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 oversee.
• Support Investigation, CAPA and changes for process equipment related topics.
• Support CQV activities (IOQ and PQ) bringing technical expertise on USP/DSP process and utilities.
• 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 with manufacturing processes such as SOP, Work Procedures, and batch reports.

Who You Are

• Master or Engineer degree, specialized in engineering science/biotech or related programs.
• 3+ years relevant experience minimum on a similar role.
• Verbal and written communications skills in both English and French.
• Understanding of processing equipment and operations used to manufacture biotherapeutics.
• Experience with equipment commissioning, qualification, and validation activities.
• 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 would be a plus.
• 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.