Executive
Cadila Pharmaceuticals Ltd
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Posted: 08 Mar 26
Job Description
JOB RESPONSIBILITIES
• Issuance of documents (SOP formats, logbook, register and LNB etc.) to cross-functional
departments based on request.
• Review of process development report/ Addendum to PDR/ Investigation report.
• Review and approval of Analytical Method Validation protocol and report.
• Review vendor qualification documents, vendor qualification report and performed vendor audit as
and when required.
• Review and approval of Specification and STP.
• Handling of QMS like change control, incident and CAPA.
• Receiving of outside sample and distribution to concerned department.
• Co-ordinate with R&D, ADL, PERL, RA & Plant QA for PDR and analytical related activities.
• Monitoring of GLP activity in analytical laboratory and R&D lab.
• Handling of internal audit.
• Routine lab monitoring in ADL, Synthesis lab & PERL.
• Tracking of SOP effectiveness and review requirements.
• Handling of SOP management system.
• Review and approval of outside sample testing and analytical test report.
• Other work allocated by DQA head as per requirement.
Job Particulars
Education Any Graduate
Who can apply Freshers
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id2854320
Job Category Sales and Marketing
Locality Address
State Gujarat
Country India
About Company
Cadila Pharmaceuticals Ltd
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