Description

* 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