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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 7 years' experience in pharmaceutical manufacturing processes ? And at least 1 year experience as an expert on deviations management? Don't hesitate to contact me: email@example.com
The mission consists on the following tasks:
- Lead on deviations and investigations related to equipment cleaning by working with operators, production managers, validation team and QA - Drive the definition of suitable CAPAs linked to cleaning deviations and the implementation of them - Ensure any change needed in cleaning controlled documents - Contribute to the definition of the daily rouging management process - Contribute to Continuous improvement related to the equipment cleaning process, in collaboration with the BPP team
- At least 7 years' experience in pharmaceutical manufacturing processes, especially biological processes - At least 1 year experience as an expert on deviations management and investigations methodology required - Experience with Equipment Cleaning, rouging treatment required - Excellent quality understanding in GMP-regulated environment - Excellent communication skills, as interacting with different teams/stakeholders: operators, production managers, validation team, quality unit - Excellent time-management skills, and experienced to work pro-actively to achieve given milestones and objectives - Fluent in French and good knowledge in English
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