Ingénieur de Production Aseptique

Jobup; Neuenburg; Vor Ort; CHF 90.000 - 120.000; Vollzeit

Zusammenfassung

Expleo invites a highly skilled Aseptic Production Engineer to join its Neuchâtel team in French-speaking Switzerland. The role ensures continuity of production, strengthens process robustness and drives continuous improvement across aseptic and sterilised operations under GMP.

The candidate will lead root cause analyses, support CAPEX projects and coordinate with QA, Maintenance and Supply Chain to optimise reliability and alignment with strategic objectives.

Qualifikationen

• 5+ years of experience in pharmaceutical/biotech production management.
• Experience in sterile aseptic processing and sterilisation within GMP.
• Strong continuous improvement experience; certification is a plus.
• Fluent in French with professional English skills.

Aufgaben

• Ensure production compliance and reliability with GMP expertise.
• Collaborate with other departments to limit unforeseen events and implement remediation plans.
• Support CAPEX projects and coordinate with Supply Chain to optimise the production plan.

Kenntnisse

Production management

Continuous improvement

GMP knowledge

Ausbildung

Master's degree

Jobbeschreibung

Expleo offers a unique range of integrated engineering, quality and strategic consulting services for digital transformation. In an unprecedented technological acceleration context, we are the trusted partner of innovative companies. We help them develop a competitive advantage and improve the daily lives of millions of people.

Joining Expleogroup means 17,000 employees in 30 countries but also:

• Technical and human support for each project and effective career monitoring
• Training to develop professional skills
• Participation in dedicated special events
• Joining a dynamic team

To support our growth in French-speaking Switzerland, we are looking for a consultant based in French-speaking Switzerland, Neuchâtel region:

Aseptic Production Engineer M/F

Your mission: The production engineer ensures the continuity of activities, strengthens process robustness and supervises the continuous improvement of production operations (aseptic and sterilised processes), while translating strategic operational excellence initiatives into actions.

• You ensure production compliance and reliability by providing technical and GMP expertise. You manage quality events related to production (change control, deviations, CAPA, complaints): conduct root cause analyses and necessary investigations.
• You collaborate with other industrial departments to limit unforeseen events and develop remediation plans: support qualification, validation and metrology activities with the QA department; collaborate to improve machine availability with the Maintenance department.
• You support the implementation of CAPEX projects related to production processes and equipment, and collaborate with the Supply Chain to optimise the production plan.

Your profile:

• Master's degree in Production, Process Engineering or Pharmaceutical Quality Assurance
• You have at least 5 years of experience in pharmaceutical/biotech production management, necessarily in a sterile environment with aseptic processing and sterilisation operations in a GMP context.
• You have genuine experience in continuous improvement methodology; certification is a plus.
• You are fluent in French and have professional English skills.