OfficerJobs Opening in Cadila Pharmaceuticals Ltd at Ankleshwar
FEATURED JOBOfficer
Cadila Pharmaceuticals Ltd
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Posted: 19 Jun 26
Job Description
• To maintain and adherence of the GLP and safety procedures in laboratory.
• To raise the request for issuance of formats, specifications and Test Methods.
• To follow the instruction of In charge for planning.
• To acquire training from concerned person to update the cGMP system update technical knowledge.
• Preparation of SOP, CAPA closer note, Specification, Test Method, Analytical Report, Analytical Protocol, stability study Analytical Report and Stability study Analytical Protocol for Raw material, Packing Material, In-process, intermediate, Finished Drug substances and Recover solvents.
• Raise change control and in laboratory and approve it in LIMS system.
• Take all prints of document and checked from concerned section head then signed and make effective the document for use.
• Provide training to all concern persons and provide Training tracker to QA for closing of change control.
• Ensure CFR 21 part-11 compliance and follow the SOP/STP for analysis to maintain proper data integrity.
• Ensure that all documents required for Regulatory Compliance are maintained properly.
• To maintain the GLP and GMP practices & ensure standards procedures in Quality Control laboratory followed effectively.
• To ensure awareness about the MSDS for concern persons.
• To co – ordinate with cross function department for cGLP systems and its maintenance, up-dation.
• To co – ordinate with EHS for safety and environment related activities and its management.
Job Particulars
Role head quality
Education Any Graduate
Who can apply Freshers
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id2909981
Job Category Quality Control
Locality Address
State Gujarat
Country India
About Company
Cadila Pharmaceuticals Ltd
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