Cadila Pharmaceuticals Ltd. (CPL) is one of India’s most reputed, research-based, techno-savvy pharmaceutical companies with a focus in the area of Formulations & APIs and having its corporate office at Bhat, Ahmedabad and State-Of-Art manufacturing facilities compliant with USFDA, MHRA, TGA, MCA, MCC & WHO norms at Dholka, Ankleshwar, Kadi and Jammu. With Diversified operations including Manufacturing of Hospital Disposables, Diagnostics, Laboratory Chemicals, Pharmaceutical Machinery, Animal Health Formulations, Feed Supplements and Bio-fertilizers, CPL is all set to forge ahead, rising to new challenges, in its quest for excellence.
Position : Executive to Asst. Manager IPQA only ApI Industry
No of Post : 3
Duration : 5 – 7 years
Location : Ankleshwar
Desired Profile : B.Sc Chemistry/M.Sc Chemistry
Job Description :
- Plant Rounds to ensure cGMP compliance
- Preparation and maintenance of IPQA audit reports and compliance with appropriate CAPA
- Review of online documentation in warehouse, production & engineering and filled batch process records.
- Preparation of release label and review of manufacturing records for batch release.
- Regular followup with plant personnel and coordination to ensure implementation of CAPA.
- Review of equipment preventive maintenance & instrument calibration records.
- Issuance of documents to all departmentsIssuance of documents to all departments.
- Internal and external audit related works.
- General documentation & co-ordination for cGMP compliance.
- Preparation & review of process validation protocols & reports.
- Support for cleaning validation and equipment qualification.
- Regulatory related documents review and submission.
- Other jobs as and when required works of QA.
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