Consultant Ingénieur Procédés Pharmaceutiques H/F
Offer details
Wanted profile
- Diploma Engineer or equivalent BAC+5 with a speciality in process engineering
- 10+ years' experience in process engineering or production in the pharmaceutical industry
- You have worked with different galenic forms: dry, liquid, pasty, sterile, etc.
- Ideally good knowledge of granulation, compression and lamination
- Knowledge of the specific requirements of the pharmaceutical/medical device/biotech industry
- Service and communication skills required for cross-functional work
- Ability to work in project mode
- Operational English you are able to work in an English-speaking professional environment
Are you interested in these assignments? Are you thinking about new opportunities for 2024 and looking for new challenges in the Life Sciences sector?
Don't hesitate to contact us!
Context
At Anywr.Life - we specialise in life sciences, and we take care of your mobility project from A to Z, whether in France or abroad.
Our specialists in the life sciences sector are here to help you:
Finding your future job? Changing region? Finding your future home? Enrolling your children at school? Saying goodbye to administrative hassles? It's easy with ANYWR, we're experts in these matters!
As part of our expansion, we are recruiting for the following profiles Process Engineering Consultant for the pharmaceutical industry.
Job offer CDI Anywr France
Mission
Your main task will be to provide technical and management solutions for our customers in the pharmaceutical industry to improve the performance and quality of their environment.
You will work directly on our partners' sites in a GMP environment, in project mode. Your tasks will be based around 3 main activities linked to industrial development (scale-up), industrial transfers and process validation.
Your role as Pharmaceutical Process Consultant will be to contribute to our customers' projects such as :
- Designing and implementing new processes and equipment in pharmaceutical production units
- Implementing a validation strategy for industrial transfer projects (risk assessment, feasibility tests, drafting validation protocols, process validation, etc.)
- Participating in risk and criticality analyses for equipment qualification and process validation
- Draft the various quality documents (specifications, protocols, reports, etc.)
- Participating in investigations following the identification of anomalies by the QA department or following customer complaints
- Follow process-related CAPAs,
- Manage the Change Control associated with projects to improve or modify manufacturing processes
- Training teams
