3 Glp Documentation Jobs

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1.0 - 3.0 years

0 Lacs

india

On-site

Company Description At TAPI, we're not just a companywe're a community committed to advancing health from the core. As the world's leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we're shaping the future of health worldwide. Our strength lies in our peoplea team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that t...

Posted 2 weeks ago

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3.0 - 7.0 years

0 Lacs

ahmedabad, gujarat

On-site

In this role, you will be primarily focused on ensuring that analytical instruments and laboratory systems are calibrated and/or qualified, maintained, and documented to GLP/regulatory expectations. Your responsibilities will include managing equipment breakdowns and lifecycle, standards, compliance documents, and supporting audits/inspections. - Calibration & Standard management: - Execute and document calibrations for analytical instruments (HPLC, GC, balances etc.). - Maintain traceability of records. - Manage calibration records, calibration labels/tags, and calibration status dashboards. - Handle the receipt, storage, issuance, and disposal of standards while maintaining their traceabil...

Posted 3 weeks ago

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6 - 10 years

5 - 12 Lacs

Rajkot

Work from Office

Job Summary: We are looking for a highly motivated and detail-oriented Assistant Manager Quality to join our quality team. The ideal candidate will be responsible for overseeing quality assurance (QA) and/or quality control (QC) activities to ensure compliance with regulatory standards (cGMP, WHO, FDA, etc.) and internal quality policies. This role is vital in maintaining product integrity and supporting continuous improvement initiatives. Key Responsibilities: Supervise and support QA/QC operations, including IPQA, documentation, and in-process checks. Ensure adherence to GMP guidelines and regulatory requirements in manufacturing and packaging. Review and approve quality-related documents ...

Posted 5 months ago

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