| Job Description: |
Prior experience mandatory in medical devices domain,
Plan, lead & co-ordinate project execution & validation activities in alignment with ISO 13485, ISO 14971.
Support validation planning & execution (IQ,OQ,PQ) for equipment, process & product transfers.
Author & review validation documentation,
Collaborate with cross functional teams,
Coordinate with customer, manufacturing plant & off shore team to ensure project continuity and on time delivery.
contributed as PM/PL will be an added advantage
Role Descriptions: Prior experience mandatory in medical devices domain|Plan| lead co-ordinate project execution validation activities in alignment with ISO 13485| ISO https://urldefense.proofpoint.com/v2/url?u=http-3A__14971.Support&d=DwIGaQ&c=euGZstcaTDllvimEN8b7jXrwqOf-v5A_CdpgnVfiiMM&r=uPVyrU0-wRkYMC7tELyR3Z2KXITAdfezxPfpSF43vug&m=RVxS_JwooPQFdYeMzKmvh-lgzIyxyV649YKyUm76Mce3OWQpLxPPFbYXKcVDewro&s=idmxbjXM9mTxoFSioTGFpjEYP1IPrrAPrjPtJpdBLo8&e= validation planning execution (IQ|OQ|PQ) for equipment| process product transfers.Author review validation documentation|Collaborate with cross functional teams|Coordinate with customer| manufacturing plant off shore team to ensure project continuity and on time delivery.contributed as PMPL will be an added advantage
Essential Skills: RD engineer
Desirable Skills:
Keyword:
Skills: Life Sciences - Regulatory Affairs
Experience Required: 6-8
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