Execution of all activities related to qualification and periodic requalification of production machines, utilities (e.g., HVAC, PRW, Compressed Air, Nitrogen, etc.), laboratory equipment, and the validation of related computer systems (CSV) in compliance with Good Manufacturing Standards, national and international regulations, and company policies.MAIN RESPONSIBILITIESPerform, directly or with external support, qualification activities (IQ / OQ / PQ and Final Qualification Reports) of plants, machines, utilities, and controlled contamination environments according to planning;Draft and review qualification protocols for GMP equipment;Assist in drafting URS and S.A.T. / F.A.T.;Collaborate with relevant personnel to evaluate and complete activities required by change control related to qualifications, ensuring compliance with procedures and timelines;Assist in drafting and updating SOPs related to the management and validation of equipment, utilities, and controlled contamination areas.QUALIFICATIONSMaster’s degree in technical or scientific disciplines;Good knowledge of cGMP;Proficiency in written and spoken English.Company DescriptionFor over 30 years, Lesaffre has been committed to Human Health & Nutrition as part of its mission to Better Nourish and Protect the Planet. In November 2018, Lesaffre acquired Gnosis Advanced Biotech and integrated it with Lesaffre Human Care to form Gnosis by Lesaffre. We are dedicated to developing and delivering nutritional actives, probiotics, and functional yeasts that promote human health and wellbeing, leveraging microorganisms and biotransformation processes like fermentation. Our vision: At Gnosis by Lesaffre, we aim for a world that moves better, digests better, ages better, feels better, and lives better through microorganisms and biotransformation.J-18808-Ljbffr
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