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2 - 6 years
3.0 - 5.0 Lacs P.A.
Gandhinagar
Posted:3 months ago| Platform: 
Work from Office
Full Time
Ensure product quality and regulatory compliance (MDR, QMS). Assist in SOPs, audits, documentation, and ISO 13485:2016 compliance. Support QC, microbiological testing, complaints, training, and regulatory updates. Required Candidate profile Experience in ISO 13485:2016, cGMP, EU MDR 2017/745, documentation, QA, and audits. Knowledge of microbiological testing, lab maintenance, compliance, problem-solving, and strong communication.
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