.. established in 1973, has played a pivotal role in the group's success. With a full-fledged ISO and WHO-GMP certified manufacturing unit in Hyderabad, India, the company has established a strong presence in both domestic and international markets. Role Description This is a full-time, on-site role for .. read more
Company :
Sain Medicaments Pvt Ltd.
QMS & Vendor Qualifications:
To initiate, review and close change controls and co-ordinate with cross functional teams.
To prepare and review Quality Risk Management documents.
To initiate and review the deviations and co-ordinate with cross functional teams.
To log and investigate the market complaints and co-ordinate with cross functional teams.
To maintain the logs of all the QMS elements like deviations, change controls, market
complaints and incidents etc.
To perform investigations where ever applicable for all the QMS tools.
To procure vendor qualification documents from the vendors / suppliers.
To plan for the on-site audits.
To prepare approved vendor list and approve the vendor / supplier in the ERP.
Shall be responsible to prepare the APQR schedule and APQR.
Artworks approvals and shade cards management.
Documents issuance and archival.
Required Experience, Skills and Qualifications
· Experienced in Quality Assurance
· Knowledge and working in IPQC area
· Leadership skills
Experience:
· 2 - 3 years & Freshers with relevant experience.
Qualification:
· B.Pharmacy, M.Pharmacy.
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