Pharma api jobs in Diu

 ...USV (Pharma) is Hiring for USFDA Formulation (OSD & Sterile) Manufacturing Plant. Location : Daman near Vapi (Gujarat). Position : Senior Manager Department : Plant - Commercial / GST Reporting to : Plant Head Key Responsibility Areas: 1. Sales Register : Take... 

 ...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 secondary review of analytical... 

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-...

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...

Raw Material Testing: Perform physicochemical and instrumental analysis (HPLC GC UV FTIR Titrations) of raw materials and excipients. Compliance & Documentation: Maintain test records COAs and laboratory documentation as per GMP GLP and data integrity guidelines...

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...

Environmental Monitoring: Conduct regular environmental monitoring of critical areas including clean rooms production areas and laboratories to ensure compliance with microbial limits. Microbial Testing: Perform microbiological testing on air surface water and personnel...

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...

Oversee daily field operations for NLG-based projects across Navsari and adjacent regions. Coordinate and supervise field teams ensuring adherence to standard operating procedures and project timelines. Track and analyze field performance using KPIs; deliver actionable...

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 ...

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...

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...

Overall responsibility for EHS compliance as per statutory ISO and internal standards. Ensure legal compliance timely filing of returns licenses and liaison with statutory authorities (PCC Fire etc.). Lead EHS audits (internal external regulatory & customer) and...