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Posted:4 days ago| Platform: 
Work from Office
Full Time
Experienced Candidates in QA as per ISO 13485 review batch records, handle deviations, CAPA, and audits; support validations; write and maintain SOPs; coordinate with cross-functional teams, documentation, and Compliance with regulatory standards. Required Candidate profile Graduate / Post Graduate in biotechnology / bio medical / Microbiology / Chemistry with strong hands on experience in QA operations in any Pharma or medical devices company.
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Hyderabad
3.0 - 5.0 Lacs P.A.
6.0 - 9.5 Lacs P.A.
8.0 - 10.0 Lacs P.A.
3.0 - 8.0 Lacs P.A.
Varanasi, Bengaluru
7.0 - 12.0 Lacs P.A.
Ahmedabad
Experience: Not specified
2.0 - 2.0 Lacs P.A.
Hyderabad
3.0 - 7.0 Lacs P.A.
Patiala
5.0 - 9.0 Lacs P.A.
Experience: Not specified
2.25 - 2.5 Lacs P.A.
3.5 - 6.0 Lacs P.A.
