Senior General Manager Job in Cadila Pharmaceuticals Ltd at Dholka
FEATURED JOBSenior General Manager
Cadila Pharmaceuticals Ltd
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Posted: 22 Jul 26
Job Description
To ensure compliance of plant as per cGMP requirements laid down by various international and national regulatory bodies.
To update quality systems & procedures in accordance with the current regulatory expectations and guidelines.
To ensure successful audits by various international / national regulatory bodies and compliance.
To ensure product Licenses permission are maintained/ renewed timely for all products manufactured at the facility.
• To ensure the implementation and maintenance of Current Good Manufacturing Practice (cGMP) standards and international quality standards in main Pharma.
• To ensure that the product meets the defined standards for strengths, identity, safety, purity and quality by various system-driven approaches.
• Create and maintain Quality Systems that are in compliance with various quality standards and regulations that mainly include FDA Regulations.
• Ensuring timely reporting of OOS, OOT, FAR and Deviations, adequate root cause investigations and compliance to scheduling and completion of resulting action items.
• To ensure timely review and approval of change controls, deviations, OOS, OOT, CAPA and QMS documents.
• To hold the manufacturing and packaging processes, if the norms are not followed and work is compromised as per Good Manufacturing Practices and the Standard Operating Procedures requirements.
• Monitoring of Quality KPI & Quality council meetings.
• Planning and scheduling of compliance audit at sites for all time readiness of regulatory audits.
• To review and update quality system and procedure of Warehouse, production, QA & QC to meet the international / national CGMP requirements.
• To ensure smooth technology transfer of new product to plant level sign the Technical Agreement with customers.
• Authorizations of SOPs, MMD I, BPR, Qualification & Validation protocol & reports, Quality Manual, VMP, SMF,QMS, PQR Validation documents and other Master documents.
• To ensure cGMP related training program for all concerned man power in coordination with HR.
• To qualify vendor of Raw & Packaging Materials.
• To highlight and resolve quality related issues at manufacturing locations.
• To ensure implementation of written procedures and guidelines.
• To ensure functioning and related activities of the RQA department at F&D.
• Responsible for Approval of Certificate of Conformance.
• Responsible for batch disposition decision and Batch release documents.
• Responsible for approval and authorization of Quality Documents viz. Quality Agreements, Declaration, submission documents.
• To ensure completion of any additional task assigned by the senior management, if any.
Job Particulars
Role head quality
Education Any Graduate
Who can apply Freshers
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id2928379
Job Category Quality Control
Locality Address
State Gujarat
Country India
About Company
Cadila Pharmaceuticals Ltd
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