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Our client is a global biopharmaceutical company focusing on creating value for people living with neurology and immunology conditions
Do you have at least 2 years' experience in drug product development within the biopharmaceutical industry? Don't hesitate to contact me : firstname.lastname@example.org
The main activities will be:
- Support the definition of DP processes for different types of formulation (liquid in vials, PFS or other container, solid) and any other more innovating formulation - Provide all appropriate support to drug product process development activities - Support any technical transfer activities up to Phase 3 inclusive - Provide support to ensure timely delivery of Clinical trial material - Ensure products are manufactured in accordance with quality system, cGMP and latest regulatory requirements - Preparation of protocols and reports in relation to drug product development activities - Ensure appropriate batch record review
- Min. 2-3 years experience in drug product development and steriles manufacturing within the biopharmaceutical industry - Previous experience in biologicals sterile fill & finish parenteral drug product manufacture and development - Experience of failure investigations, process improvement and QbD principles - Technical experience in parenteral liquid and lyophilized product development and cGMP manufacturing under aspetic conditions - Good technical knowledge of sterile drug product development - Good knowledge of cGMP and regulatory requirements - Excellent communication, negotiation and team player skills
what do we offer?
We offer an attractive salary with extra-legal advantages : - Group insurance - Hospitalisation insurance - Meal vouchers of 7 euros gross per working day - Reimbursement km or company car - Monthly allowance (50 euros net per month) - A 13th month - Training - Etc A rate as freelance is also possible.