- 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.

**Contact: Marion Buttay**
**Quote job ref: JN-032026-6969131**