Job TitlePrior experience mandatory in medical devices domainPlan, lead & co-ordinate project execution & validation activities in alignment with ISO 13485, ISO 14971Support validation planning & execution (IQ, OQ, PQ) for equipment, process & product transfersAuthor & review validation documentationCollaborate with cross functional teamsCoordinate with customer, manufacturing plant & offshore team to ensure project continuity and on time deliveryContributed as PM/PL will be an added advantageSkills: Life Sciences - Regulatory Affairs Experience Required: 6-8