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Teyro Labs is a pharmaceutical company based in Chennai, India. It specializes in the development and manufacturing of niche finished dosage formulations and Active Pharmaceutical Ingredients (APIs). The company is known for its focus on oncology and high potency products.
We are Hiring
Position: Sr. Exe. / Asst. Manager/ Manager
Department: QA (Audit & Complaince)
Qualification: M.Pharm / B.Pharm, M.Sc/B.Sc, M.Tech/B.Tech/BE
Experience: 5-15 Years
Job Description:
•Monitoring of site quality system and compliance as per applicable regulatory requirements (USFDA, EMA, ANVISA and other regulatory requirements).
•Support and facilitate Regulatory Inspections and Customer Audits.
•Facilitate timely preparation of inspection response and monitor implementation of various compliance actions / CAPAS arises due to regulatory inspections / customer audits.
•Ensure all time inspection readiness for any regulatory or customer audit at manufacturing site.
•Review and evaluate site compliance with internal policies and procedures.
•Check / verify compliance of manufacturing site against 483’s issued to various compliance. Perform gap assessment, identification of actions wherever gaps identified, tracking and closure of CAPA’s.
•Initiation and implementation of Quality initiatives as per updated / new regulatory guideline requirement.
•Provide strategic and compliance related inputs manufacturing site.
•Stay abreast of regulatory changes in the industry.
Contact us: +91 9790979646
Teyro Labs HR Email ID:
hr@teyro.com
www.teyro.com
Location: Oragadam, Chennai
