At Sun Pharma, we commit to helping you "Create your own sunshine"-- by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
Are You Ready to Create Your Own Sunshine
As you enter the Sun Pharma world, you'll find yourself becoming 'Better every day' through continuous progress. Exhibit self-drive as you 'Take charge' and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we 'Thrive together' and support each other's journeys."
Key responsibilities:
This role is responsible for overseeing the operations of a specific block within the manufacturing facility, ensuring efficient production processes, compliance with quality and safety standards, and meeting production targets. This role will report to the Block head. To meet the production targets
Production capacity of 6 Billion in OSD with handling 20 lines
.
Handling Team size of 100 people
To ensure the implementation of current Good Manufacturing Practices and SOPs at work place
To maintain and improve the product quality as per standard
To ensure Accuracy, Reliability, validity, integrity and completeness of the cGxP data/records
To plan the department activities as per weekly delivery schedule for OSD and Liquid orals
To ensure the effective control on man, machine and material in the department
To participate and coordinate various on-going qualification and validation activities
Collaborate with the site quality head, QA & QC head in ensuring that the production is aligned to the quality standards and regulatory requirements
To ensure the completeness of all the trainings (Sops, Technical, Developmental and Regulatory etc.) assigned to block personnel's
To organize and implement the on-job training activities in the department
To ensure the implementation of EHS practices during work
To ensure the maintenance of equipment and upkeep of department constantly
To control the rejection during manufacturing and packing operations
To do counseling and grievance handling of the subordinates
To prepare, review and approve the Standard Operating Procedures
To evaluate deviations, change controls and other quality documents for appropriate conclusion
To ensure the market compliant investigations as per the track wise module and its timely closure and awareness training to all the concerned persons
Handling of QMS related activities of Block
To carry out the batch failure investigation for root cause identification and accordingly appropriate corrective action and preventive action taken
To review and approve the equipment qualification protocols, process validation protocols, reports, specifications and master formula
Travel Estimate
Job Requirements
Educational Qualification
M.Sc / B.Pharm / M.Pharm
Experience
Tenure: 15 to 17 Years
Your Success Matters to Us
At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let's create a brighter future together!
Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).
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