Senior Executive - Tablet Production

About the Role

Join our Sun Pharma global operations team as a Senior Executive located in Halol 2. At Sun Pharma, we empower you to take ownership of your career progression, grow continuously, and be part of a supportive community where collaboration and excellence thrive.

Key Responsibilities

• Authorized to sign cGMP documents including equipment sequential logs, temperature and humidity records, cleaning records of manufacturing areas, balance calibration, in-process and test approval labels, tool set cleaning and utilization records.
• Oversee batch manufacturing records and manage in-process and finished product test requisitions.
• Maintain records for bulk quarantine and staging room materials movements.
• Manage daily production activities of the Tablet department’s FBE section ensuring production targets for quantity, quality, and GMP compliance are met.
• Assist in establishing and updating systems and procedures compliant with Good Manufacturing Practices (GMP).
• Coordinate validation and GMP compliance activities alongside Quality Assurance and Quality Control departments.
• Conduct GMP training sessions for staff and operators across all departments.
• Optimize utilization of resources including manpower, materials, and machinery in the department.
• Prepare daily activity reports to document the status and progress of operations.
• Manage validation, calibration, and qualification activities for equipment and products.
• Handle procurement and indenting for machinery, spare parts, change parts, and departmental materials.
• Prepare and execute destruction notes as required.
• Maintain GMP documentation, such as equipment logbooks and housekeeping records.
• Train subordinate staff and coordinate manpower efforts to achieve organizational and GMP standards.
• Standardize production processes to enhance efficiency and product quality.
• Assume role responsibilities of other Officers during their absence.
• Coordinate with departments such as Warehouse & MIS for materials scheduling and Engineering for preventive maintenance.
• Develop and revise Batch Manufacturing Records (BMR), Standard Operating Procedures (SOP), and protocols for new products and equipment, ensuring proper execution.

Job Requirements

• Educational qualification: Bachelor’s or Master’s degree in Pharmacy (B.Pharm/M.Pharm).
• Experience: Minimum of 2 years in a relevant pharmaceutical production or manufacturing environment.

Additional Information

Sun Pharma prioritizes your success and well-being by offering robust benefits and opportunities for personal and professional development. This job description outlines general responsibilities and may be modified to meet business needs, including assignment of comparable duties aligned with your skills and experience.