Ingénieur Process Pharma

Exyte GmbH; Lyon; On-site; EUR 70,000 - 110,000; Full time

Job summary

Exyte is seeking a Process Engineer to lead and coordinate design activities for biopharmaceutical facilities in Lyon, France. You will drive process design and clean utilities, ensuring safety, GMP compliance, and cost-effective solutions across project phases.

You will collaborate with international teams, mentor junior engineers, and contribute to HAZOP reviews, FATs/SATs, and the development of P&IDs and mass balances. Fluency in French and professional English are required.

Qualifications

• Master degree or equivalent in an engineering field.
• Min. 5–10 years in the design of biopharmaceutical facilities.
• Detailed knowledge of GMP and safety regulations.
• Fluent in French and professional English language skills.

Responsibilities

• Works independently in all areas of process design.
• Leads general room layout during facility design.
• Participates in HAZOP and GMP reviews, FATs, SATs.
• Specializes in design areas like Clean Utilities and Pharmaceutical Process.
• Supports project teams across all project phases.

Skills

French fluency

English proficiency

Mentoring

Education

Master’s degree in engineering

Job description

Discover your exciting role

The Process Engineer is responsible for leading and coordinating all pharmaceutical process and clean utilities engineering activities on complex industrial projects for the biggest pharmaceutical companies and for the local ones. The Process Engineer will progress within an international company specializing for EPC and EPCM projects. Exyte is major actor in the following business areas: Biopharma & Life sciences, Advanced technology facilities, Data centers.

The role ensures delivery of safe, compliant, and cost-effective design solutions while managing interfaces, quality, schedule, budget, and according to your experience also the discipline resources. The Process Engineer provides technical leadership for its discipline to project teams and supports the execution through all project phases.

Explore your tasks and responsibilities

• Works independently in all areas of process design
• Uses and improves of internal standard tools/procedures/checklists
• May train lower-level engineers
• Shows understanding of project budget and schedule
• Understands and serves all project related interfaces to other disciplines
• Work package owner
• Leads in general room layout during facility design
• Experienced in Block Flow/Process Flow Diagrams,mass balances as well as Remastering/Issuing ofP&IDs
• Participation in HAZOP and GMP reviews, FATs, SATs
• Specialize in the specific area of design likeClean Utilities (PW, WFI, CS, CIP…) and/orPharmaceutical Process (USP, DSP, Formulation, Bloodfractionation, etc..).

Show your expertise

• Has experience in all design phases of a project
• Min. 5-10 years experiences in the design of biopharmaceutical facilities
• Master Degree or equivalent in a related engineering field.
• Detailed Knowledge about facility and equipment design as well as all GMP and Safety relevant regulatory
• Fluent in French and professional language skills in English.