Executive - Tablet Production Department

About Sun Pharma

Sun Pharma is dedicated to helping individuals "Create your own sunshine" by nurturing an environment that promotes continuous personal and professional development, empowering employees to lead their own growth and thrive within a supportive team atmosphere.

Joining Sun Pharma means embracing the values of "Better every day" through consistent progress, showing self-motivation by taking initiative and leading confidently, and fostering teamwork with the belief that "We thrive together" through mutual support.

Primary Responsibilities

• Authorized signatory for cGMP-compliant documentation including equipment sequential logs, temperature and humidity logs, daily to monthly cleaning records of manufacturing areas, balance calibrations, in-process and under-test approval labels, and tool set usage and cleaning records.
• Sign-off on Batch Manufacturing Records (BMR), in-process and finished product test requisitions, and bulk quarantine/staging room in-out logs.
• Manage day-to-day production activities within the Tablet department's FBE section, ensuring the achievement of production targets in quantity and quality while maintaining GMP adherence.
• Assist fellow officers in manufacturing and control functions related to the Tablet department.
• Support the establishment, maintenance, and updating of procedures in line with Good Manufacturing Practice guidelines.
• Collaborate with Quality Assurance and Quality Control departments on validation, GMP, and product quality matters.
• Conduct GMP training for staff and operators across departments.
• Optimize departmental resources including manpower, materials, and machinery.
• Prepare daily activity reports concerning departmental operations.
• Oversee calibration, qualification, and validation processes for equipment and products within the department.
• Manage procurement requests for machinery, spare parts, change parts, and required materials.
• Prepare and execute destruction notes as necessary.
• Maintain GMP documentation such as equipment logbooks, environmental monitoring, and housekeeping records.
• Train subordinates and manpower to align with organizational goals and ensure GMP compliance.
• Guide teams to standardize production processes, enhancing efficiency and product quality.
• Act as Officer in Charge during the absence of the designated officer.
• Coordinate with Warehouse & MIS for material requirements to meet production schedules, and collaborate with Engineering for preventive maintenance planning.
• Prepare and revise Batch Manufacturing Records (BMR), Standard Operating Procedures (SOP), and Protocols for new products or machinery, and ensure their proper execution.

Job Requirements

• Educational Qualification: Bachelor’s or Master’s degree in Pharmacy (B.Pharm / M.Pharm).
• Professional Experience: Minimum of 2 years in related manufacturing operations.

Your Success Matters

At Sun Pharma, your growth and well-being are highly valued. We offer comprehensive benefits and opportunities designed to promote personal and professional advancement. Join us in making a meaningful impact every day as we build a brighter future together.

Additional Information

This job description outlines the general duties and level of work expected for this role but is not exhaustive. Responsibilities may evolve over time, and the employer may assign duties consistent with the employee’s qualifications and experience.