Average salary: Rs1,325,000 /yearly
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Rs 15.16 - 40.21 lakhs p.a.
...Department : Plant - Commercial / GST Reporting to : Plant Head Key Responsibility Areas: 1. Sales Register : Take dump from SAP verify invoices against data for HSN code taxable value tax rate and amount place of supply scheme used etc. and report discrepancy if...SAPFull timeRs 1.9 - 8.87 lakhs p.a.
Laboratory Management: Oversee the daily operations of the QC Raw Material section including work allocation shift planning and ensuring the timely testing and release of APIs excipients and packaging materials to support production schedules. Data Review & Approval: Perform...SuggestedFull timeShift workRs 8.36 - 16.88 lakhs p.a.
Production OSD: Assistant Manager Production Operations Leadership: Lead and oversee daily manufacturing schedules across Granulation Compression Coating and Capsule filling sections to consistently meet production targets and optimize line efficiency. QMS Management...SuggestedFull timeShift workRs 8.36 - 16.88 lakhs p.a.
Documentation & Document Control: Manage the complete lifecycle (preparation issuance retrieval and destruction) of all QA documents including SOPs Logbooks BMRs and BPRs while maintaining the documentation cell . In-Process Quality Assurance (IPQA): Conduct line clearances...SuggestedFull timeRs 1 - 6.87 lakhs p.a.
...Preventive Maintenance (PM) Tracking: Track schedule and document factory-wide Preventive Maintenance schedules and calibration programs for processing machinery and critical utilities. Data Integrity Enforcement: Ensure all engineering logbooks BMS/SCADA trend records...SuggestedFull timeFor contractors- ...resolution. Ensure accurate timely collection documentation and reporting of field data. Lead training sessions and onboarding programs for new field personnel. Manage logistics resource allocation and distribution of equipment and materials to field teams. Resolve...SuggestedFull timeWork at office
Rs 8.36 - 16.88 lakhs p.a.
Equipment Qualification: Prepare review and approve Design Qualification (DQ) Installation Qualification (IQ) Operational Qualification (OQ) and Performance Qualification (PQ) protocols and reports for OSD equipment (e.g. Rapid Mixer Granulators Fluid Bed Dryers Compression...SuggestedFull timeRs 15.16 - 40.21 lakhs p.a.
...optimization waste reduction energy & water conservation initiatives. Ensure EHS documentation reporting and third-party compliance checks. Lead people development EHS training programs and capability building across the site. Required Experience: Senior Manager...SuggestedFull timeRs 1 - 8.36 lakhs p.a.
...certificates (NIST/NABL) and audit vendor execution dossiers. Preventive Maintenance (PM): Develop execute and track preventive maintenance programs for field sensors control valves actuators loop controllers and analytical instruments (e.g. pH conductivity meters). SOP...SuggestedFull timeRs 4.52 - 12.9 lakhs p.a.
Technical Transfer (TT): Sterile Executive Technology Transfer Execution: Execute the successful scale-up and transfer of sterile formulations (injectables ophthalmic lyophilized products) from R&D to commercial production lines. Process Validation: Author review and...SuggestedFull timeRs 4.52 - 12.9 lakhs p.a.
Job Description: Production OSD Executive Line Operations Management: Direct and monitor daily unit operations across Granulation Compression Capsule Filling and Coating sections to achieve production targets. QMS Compliance & Investigation: Initiate and draft shop-...SuggestedFull timeContract workShift workRs 6.87 - 17.09 lakhs p.a.
Protocol & Report Writing: Draft review and execute Analytical Method Validation Method Verification and Method Transfer protocols and final reports for various dosage forms in accordance with current ICH USP and FDA guidelines. Method Execution: Independently perform ...SuggestedFull timeRs 6.87 - 17.09 lakhs p.a.
Sterile Manufacturing Operations: Oversee aseptic filling compounding filtration and lyophilization processes to ensure product sterility and quality. Aseptic Practices & Compliance: Ensure adherence to GMP USFDA MHRA WHO and EU-GMP guidelines maintaining sterility...SuggestedFull time
