Executive to Assistant manager - QA

3 years

0 Lacs

Posted:1 week ago| Platform: Linkedin logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Company Description

Coromandel International Limited is a leading Agri solutions provider in India, operating primarily in the Nutrient and Crop Protection sectors. Known for being the second-largest manufacturer and marketer of Phosphatic fertilizers in the country, Coromandel offers an array of products including Fertilizers, Crop Protection, Bio Products, and Specialty Nutrients. The company serves both domestic and international markets, supported by an extensive network of around 750+ rural retail outlets offering comprehensive farming services. Coromandel is recognized for its environmental efforts and is part of the Murugappa Group. For more details, visit www.coromandel.biz.

Role Description

This is a full-time on-site role for an Executive to Assistant Manager - QA, located in Cuddalore. The selected candidate will be responsible for quality assessment, testing, and ensuring compliance with industry standards. Daily tasks include conducting quality audits, monitoring production processes, implementing QA protocols, and identifying areas for improvement. The role also involves coordinating with the production and R&D teams to maintain and enhance quality standards.Key Responsibilities:Preparation, review, and control of Standard Operating Procedures (SOPs), Specifications, and Batch Manufacturing Records.Support the execution and documentation of Change Controls, Deviations, CAPA, and Out of Specification (OOS) investigations under supervision.Participate in document review for accuracy, completeness, and compliance with internal quality standards and regulatory guidelines.Assist in internal audits, self-inspections, and support regulatory inspections by ensuring timely availability of records and data.Maintain and update QA documentation such as the Site Master File, Quality Manual, and Logbooks.Support vendor qualification activities through documentation and records maintenance.Preparation of Annual Product Quality Review (APQR) data collection and preparation.Monitor and ensure compliance with good documentation practices (GDP) throughout the site.Support training activities on quality systems and regulatory requirements.Coordinate with Quality Control (QC), Production, and other departments for smooth quality operations.Preparation of protocols and reports for Process validation, cleaning validation.Education Qualification:M.Sc (Chemistry), M.Sc (Microbiology), M.Sc Biochemistry, B.Pharm, BE Chemical, Etc..Experience:With 3 to 5 Years in a Pharma company (QA, QC, Microbiology)

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