Our client is a global biopharmaceutical company focusing on creating value for people living with neurology and immunology conditions.
If you have experience in the validation and development of analytical method, please, contact me : 0473/11.50.25 or by mail : email@example.com
The main activities of this position will be:
•Participate in development of analytical methods
•Participate in (co-)validation or verification of analytical methods.
•Perform daily laboratory activities related to release and stability testing
•Follow up deviations, incidents and validate the results.
•Participate to method transfers from different laboratories
•Participate in writing the documentation related to the lab activities
All these activities will be performed in compliance with the GMP/HSE rules and with the regulatory requirements for each development phase of the product.
•Bachelor degree, or master’s degree, in biochemistry or in analytical chemistry
•Previous experience preferably in the biotech industry
•Good knowledge of method validations
•Strong and proven laboratory skills
•A good practical experience and expertise in at least one of the analytical techniques used in the laboratory: HPLC/UPLC, ICP-MS, qPCR, gel/capillary electrophoresis, immunoassays.
•A good knowledge of GMP standards
•Experience with proteins
•Good interpersonal, verbal, and written communication skills with ability to balance multiple priorities
•Good knowledge of English (ability to read scientific documents)
•Well organized, flexible, meticulous and rigorous, proactive, with a strong team spirit. Rigour is required for the review of analytical data.
•Able to work in a multicultural environment.
•Mission duration : 7 months
Good knowledge of French & English
Interested ? 0473/11.50.25
We offer an attractive salary with extra-legal advantages :
•Meal vouchers of 7 euros gross per working day
•Reimbursement km or company car
•Monthly allowance (50 euros net per month)
•A 13th month
A rate as freelance is also possible