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
To ensure that the ISO14001 and ISO45001 requirements and related documents are maintained.
To execute production activities as per production planning in coordination with various department.
To review, approve and distribute the instructions for Solvent Recovery and APIs according to written instructions
Reviewing all production batch records and ensuring that these are completed and signed.
Ensuring compliance to c GMP, Safety and SOPs.
To ensure that all production deviations are reported, evaluated, investigated and corrective actions are initiated.
Production planning and target achievements with respect to quality, quantity, yield, recovery efficiency and compliance.
To review validation protocols and reports and product manuals.
To evaluate proposed change control related to process or equipment’s.
To perform full scale investigation related to OOS and OOT.
To implement corrective and preventive actions to address root cause and participates in QRB meeting.
To ensure that equipment’s are maintained in qualified state.
To ensure compliance of production documents.
Impart SOP related training to sub-ordinate and upgrade their skill & knowledge. Ensure that training records are updated in time for self and plant personnel.
To maintain shop floor discipline and high morale in employee and ensure that harmonious relations among the employees are maintained.
To ensure the plant facilities and surrounding area is clean and presentable.
To complete and ensure the annual performance review of all the related subordinates.
To ensure the solvent recovery is online with respect to c GMP, yield and quality.
To facilitate, ensure & extend support for all audits pertaining activities.
To ensure complete compliance in plants during Internal/External and Regulatory audits.
To support and to play important role in remediation strategy rolls out.
Preparing, Reviewing, Approving And Distributing The Instructions For The Production Of Intermediates Or Apis According To Written Procedures.
Reviewing All Production Batch Records And Ensuring That These Are Completed and Signed.
Making Sure That The Necessary Calibrations Are Performed And Records Kept.
Travel Estimate
Job Requirements
Educational Qualification
B.sc/M.Sc
Experience
Tenure: 10-16 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).