Assistant Manager Job in Cadila Pharmaceuticals Ltd at Ankleshwar
FEATURED JOBAssistant Manager
Cadila Pharmaceuticals Ltd
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Posted: 19 Jun 26
Job Description
• Review of validation documents (Mfg. Process, Cleaning, equipment and water validation etc.) and overall monitoring of validation activities.
• Responsible for Document Data Control.
• Internal Audits.
• Co-ordination with other department for cGMP compliances.
• Responsible for customer audits and its responses.
• Plant Round.
• Preparation and Review of Validation Master plan..
• Preparation and Review of site Master file.
• Review and evaluation of Change control, Deviations and CAPA.
• Handling of Out of Specification, Out of trend and NCR etc..
• Responsible for handling of Market complaints and fulfilment of other marketing requirements.
• Handling of returned goods and product recall.
• Approval of filled batch process records of intermediates and finished products.
• Responsible for batch release.
• Review and approval of standard operating procedure for all departments. Preparation, Review of Quality Assurance SOPs.
• Review of Quality control compliances.
• Reviewing and approval of all BPR/MPR/PQR.
• Review and approval of Equipments qualification.
• Reviewing and approval of all Master specification, method of analysis, protocol and reports.
• Responsible for Vendor Qualification.
• Responsible for approval of approved vendor list and updating.
• Co-ordinate with local FDA for various FDA related works.
• As and when as per requirement other QA works to be done.
Job Particulars
Education Any Graduate
Who can apply Freshers
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id2910026
Job Category Manufacturing
Locality Address
State Gujarat
Country India
About Company
Cadila Pharmaceuticals Ltd
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