Date de publication:11 août 2022
Type de contrat:Durée indéterminée
Lieu de travail:Vaud
EFOR-CVO is the Life Sciences offer of the EFOR Group. Result of the unionof 3 majors players in consulting: EFOR Healthcare, leader in the world of medical devices, CVO-EUROPE, a real player in the pharmaceutical industries, and Soladis, digital expert and data processing expert.
The pooling of our expertise has enabled us to consolidate our position as the European leader in Life Sciences consulting and to build a completely new offer by intervening throughout the entire life cycle of products.
Supported by our technical department, our consultants help to boost the projects of more than 350 Large Companies, SMEs and Startups in the pharmaceutical and medical devices industry!
To support our development in Switzerland, we’re looking for a:
You will be in charge of the qualification of equipment related to production for major companies in the Life Sciences Industry.
Your main tasks will be (not exhaustive list) to:
Write qualification documents related to manufacturing or packaging equipment (validation master plan, protocols, reports, etc.)
Participate, execute and/or supervise the execution of tests (IQ, OQ, PQ),
Manage non-conformities and change,
Coordinate various projects,
You have a degree in Life Sciences, engineering or equivalent by experience.
You have at least 3 years of experience in the qualification of production, manufacturing or packaging equipment in the Life Sciences Industry.
You are used to work in regulatory environment and have strong knowledge of regulatory standards related to pharmaceutical or biotechnology environment (GMP, GLP, ICH, 21 CFR, etc.).
You speak fluently French and English.
You have strong communication skills and an analytical thinking.
Your social skills enable you to work in team; you are an autonomous person on your activities.
- Myriam Jaaidane