• Drive impactful industrial and development projects in a regulated environment.
  • Contribute to process optimisation, tech transfer, and documentation.

About Our Client

Our client operates in a GMP-regulated environment, managing cross-site projects linked to product development and industrial scale-up. The organisation collaborates across multiple production and development facilities in Europe.

Job Description

• Develop or adapt steam sterilisation processes while ensuring product integrity.
• Support qualification and validation of autoclaves and associated equipment.
• Participate in process optimisation, investigations and continuous improvement initiatives.
• Prepare, justify, and structure technical documentation (protocols, reports, rationales).
• Collaborate closely with QA, Production, Engineering and the Product Development Team.
• Coordinate with the European production site when required.
• Support the development and transfer of new synthesis or manufacturing processes.
• Follow trials, consolidate data, and analyse process performance.
• Align process documentation across teams and ensure coherence.
• Act as an operational technical reference for assigned processes

The Successful Applicant

• Holds a degree in engineering, chemistry, biotechnology or materials science.
• Has at least 5 years of industrial experience in a GMP-regulated environment.
• Brings experience in pharma/medical device operations with knowledge of GDP and ISO 13485.
• Demonstrates confirmed expertise in steam sterilisation process development and validation.
• Familiar with autoclave systems such as Fedegari or Belimed.
• Autonomous, structured, proactive, with strong analytical and documentation skills.
• Excellent communicator capable of working in a multisite, multi-project environment.
• Fluent in French and English; German is a plus.

What's on Offer

• A 6-month consulting mission with strong technical impact across multiple production and development sites.
• Exposure to GMP operations and European collaboration.
• A strategic role supporting process robustness, technology transfer and documentation excellence.

Quote job ref

JN-032026-6969131

Job Function

Healthcare & Life Sciences

Specialisation

Medical devices

Industry

Healthcare / Pharmaceutical

Location

Lausanne Region

Contract Type

Interim

Job Reference

JN-032026-6969131