Sr. Officer / Executive CQA (Consumer) Third party Shalina Healthcare

5.0 - 7.0 years

10 - 14 Lacs

navi mumbai, turbhe pawane

Work from Office

Monitoring of Contract manufacturers of Consumer products across India. Quality Oversight at Contract manufacturing sites of Consumer products. Overall responsible for monitoring of Quality compliance at Consumer Sites across India. FG Inspection, Review of batch records and Batch releases Review of Finished product related data to support new Third Party Launch Monitoring of all shop floor activities IPQA Checks of Consumer products Lozenges, Toothpaste, Food, Nutraceutical products, Handwash, Sanitizer, Balm, Inhalers etc. Responsible for investigation of non-compliance with Contract manufacturer. Process Validation and Stability study execution and data review APQR preparation, Witness ma...

Posted -1 days ago

AI Match Score

Apply

Executive /Sr. Executive – CQA – Loan Licencing Shalina Healthcare

7.0 - 10.0 years

5 - 9 Lacs

navi mumbai, turbhe pawane

Work from Office

Monitoring of Loan Licence Site located in Navi Mumbai. IPQA/Shop floor activities monitoring - Tablets, Capsules, Oral Liquids, External and Sterile formulations etc. (Preferred External preparations and Oral Liquid formulations) Quality Oversight at Loan Licence Sites and tracking for closure of actions. FG Inspection, Review of batch records and Batch releases. Site pre-assessment for regulatory inspections as per GMP requirement. Investigation of any non-compliance in co-ordination with LLU Site and tracking closure of CAPA. Review and COA and analytical data before release of finished product from LLU Site. Review of Finished product related data to support new product Launch. Process V...

Posted -1 days ago

AI Match Score

Apply

Executive/ Sr. Executive – CQA- Loan Licencing Shalina Healthcare

7.0 - 10.0 years

5 - 9 Lacs

navi mumbai, turbhe pawane

Work from Office

Monitoring of Contract manufacturers, Process Validation, Stability Study, Quality Agreement, APQR, FG Inspection and batch release. Responsible of co-ordination with regional representative to harmonize Quality systems across all LLU Sites. Quality Oversight at Contract manufacturing sites on periodic basis. Protocol preparation and execution of process validation for all dosage forms-Pharma. Stability Study and review of Stability Data as per stability interval. APQR preparation, Witness manufacturing and analysis of finished product. Execution of Quality agreements with all Contract manufacturing Sites. FG Inspection, Review of batch records and Batch releases Review of Finished product r...

Posted -1 days ago

AI Match Score

Apply

Start Your Job Search Today

Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.