24 Job openings found

  Manage day-to-day administrative operations. Arrange employee and guest transportation. Handle hotel, flight, and travel bookings. Coordinate guest hospitality and accommodation. Manage office facilities, housekeeping, and security. Coordinate with vendors and service providers. Procure office supplies and maintain inventory. Monitor office maintenance and asset management. Organize meetings, conferences, and corporate events. Maintain administrative records and documentation. Process vendor bills and track ...

Key Responsibilities: Manage and oversee all Quality Control activities for formulation products. Ensure compliance with cGMP, GLP, and regulatory guidelines. Review and approve analytical reports, COA, STP, and specifications. Handle instrument operations like HPLC, GC, UV, Dissolution apparatus, etc. Ensure calibration, validation, and maintenance of QC instruments. Coordinate with QA, Production, and R&D for smooth operations. Handle ...

Direct Material Sourcing: Procure Active Pharmaceutical Ingredients (APIs), excipients, and primary/secondary packaging materials, ensuring compliance with all cGMP/pharmacopeial standards. Engineering/CAPEX Procurement: Manage the end-to-end procurement of capital equipment, plant machinery, utilities (HVAC, WTP), and engineering services for facility projects and maintenance. Vendor Management: Identify, qualify, and manage a robust base of local and international suppliers. Conduct vendor audits and ...

Job Description: Microbiology Executive / Manager We are looking for a dedicated Microbiology professional to manage and execute microbiological testing and related quality functions within our organization. The candidate will be responsible for conducting microbiology tests, ensuring environmental monitoring, and maintaining compliance with quality standards, with responsibilities varying based on experience. Key ...

  Operate, monitor, and maintain Compression machines (e.g., Parle Elizabeth – 37 Station & 51 Station). Handle Coating machines (e.g., Gansons – 60 Pan) for tablet coating processes. Manage Capsule filling machines (e.g., Pacifab LLP) ensuring accuracy and compliance. Operate Liquid Filling & Manufacturing equipment (Liquipack) for syrup, suspension, or solution formulations. Run Granulation equipment ...

Key Responsibilities:•Handling of QMS tools like change control, CAPA, Deviation etc.•Handle QA efficiently and able to maintain documentation as per GMP.•Preparation and maintenance of training schedule and co-ordinate with working staff to establish Procedures, Standards and System.•Preparation of Raw Material and Finished Product specification in accordance with Regulatory Guideline.•Vendor Evaluation, ...

Position: QC Manager Location: Palanpur, Gujarat Industry: Pharma – API Key Responsibilities: Lead and oversee Quality Control operations in compliance with cGMP & regulatory guidelines. Manage QC documentation, including qc document review, SOPs, and analytical records. Supervise laboratory activities such as RM, PM, in-process, and finished product testing. Ensure timely calibration, qualification, and maintenance of ...

Job Description: Production Executive We are looking for a Production Executive with hands-on experience in API manufacturing to join our dynamic production team. The ideal candidate will be responsible for supervising daily production activities, ensuring batch operations run smoothly, and maintaining compliance with safety and quality standards. Key Responsibilities: Execute and monitor day-to-day ...

Job Description: Microbiology Executive / Manager We are looking for a dedicated Microbiology professional to manage and execute microbiological testing and related quality functions within our organization. The candidate will be responsible for conducting microbiology tests, ensuring environmental monitoring, and maintaining compliance with quality standards, with responsibilities varying based on experience. Key ...

Key Responsibilities: Supervise daily production activities to ensure timely completion as per the batch manufacturing schedule. Implement and maintain GMP/cGMP practices and regulatory compliance throughout the production process. Monitor chemical processes, raw material usage, and handling of intermediates and final products. Prepare and review Batch Manufacturing Records (BMR) and Standard Operating Procedures (SOPs). Coordinate with ...