AQA / Sr. Executive, Dy. Manager Aragen Life Sciences Private limited

5.0 - 10.0 years

2 - 6 Lacs

hyderabad

Work from Office

1. Ensure Adherence and compliance to requirements of good manufacturing practices, GDP, EHS practices and company policies and procedures. 2. Extending support to all the key functions to establish and effectively implement the quality system and procedures to maintain a state of compliance. 3. review and approval of standard operating procedure, General testing procedure. 4. issuance and maintain distribution of SOPs, Documents, analytical documentation for internal and external purpose and formats/registers/LNB required for analytical testing activities. 5. review and approval of specification, MOA, Protocals(transfer/Miscellaneous), reports (Method validation/Transfer/miscellaneous), qua...

Posted Date not available

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Walk-Ins: QA Exe/AM/DM/Mgr in Bangalore on 23rd Aug 25 Vibonum Technologies Pvt Ltd, Nanjangud, Bangalore

4.0 - 9.0 years

6 - 15 Lacs

mysuru

Work from Office

Vibonum Technologies Private Limited conducting a Walk-in interview in Quality Assurance department for its OSD Plant at Nanjangud, Mysore. Kindly carry your, latest 3 Months salary slip, appointment letter with CTC breakup and previous company relieving letters. ----------------------------------------------------------------------------------------------------------- Open vacancies in Quality Assurance for: IPQA Manufacturing : Exe > 08-10 Yrs IPQA Packing & Warehouse : Exp > 8 - 16 Yrs QMS: Exe / Sr. Exe : Exp > 08-10 Yrs CSV / ITQA/ Electronic DI compliance : Exp > 10-12 Yrs Process Validation : Exp > 08-10 Yrs AQA / Lab QA : Exp > 08-10 Yrs Documentation Cell : Exp > 04-08 Yrs AM/DM/Man...

Posted Date not available

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QA-Assistant Manager/Dy.Manager Sterile/Injectable MJ Biopharm

10.0 - 18.0 years

12 - 17 Lacs

pune

Work from Office

Quality Management System: Oversight/Handling of Handling of Change Control, Incident / Deviation and CAPA. Following and tracking of Change Control, Incident /Deviation and CAPA. Involved in the investigation activity whenever required. Ensure that products are manufactured in compliance to Regulatory requirements and as per Good Manufacturing Practices. Ensure that production and manufacturing activities are undertaken in compliance to SOPs, systems, procedure and GMP/GLP requirements. Maintain GMP compliance in various departments to manage the production in line with the current GMP requirement. Handling of Change Control, Deviation, risk assessment and CAPA as per company procedure Veri...

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