Deputy Manager - Production (API) at Piramal Pharma Ltd

Kohir mandal, Telangana, India -

Full Time

Start Date

Immediate

Expiry Date

19 Oct, 26

Salary

0.0

Posted On

21 Jul, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

DCS Operation, GMP Practices, SAP, QMS, BMR/SOP Preparation, Data Integrity, Chemical Engineering, Production Supervision, Preventive Maintenance, Safety Compliance, Operational Qualification, Performance Qualification, DocuSign, Trackwise, Housekeeping Management, Staff Training

Industry

Pharmaceutical Manufacturing

Description

Be the First to Apply Division Piramal Critical Care Piramal Critical Care (PCC), a business unit of Piramal Pharma, is the fourth-largest producer of inhaled anesthetics and a global player in hospital generics. We are motivated by our vision of commitment to delivering critical care solutions for patients and healthcare providers across the globe while achieving sustainable and profitable growth for all the stakeholders. PCC maintains a wide presence across the US, Europe, and more than 100 countries across the globe. Its rich product portfolio includes Inhalation Anesthetics such as Sevoflurane, Isoflurane and Halothane as well as Intrathecal Baclofen therapy, for spasticity management. PCC has a strong manufacturing and process development experience with wholly-owned, state-of-the-art manufacturing facilities in the United States and India, inspected periodically by the US FDA and the UK MHRA and other regulators. The strategic locations of our facilities help us supply high-quality products around the world, timely at optimal costs. For more details, please visit https://www.piramalcriticalcare.com/global/ Job Title Deputy Manager - Production (API) Job Description 1. To handle shift as shift in charge whenever required. 2. Follow instructions from Manager for the general shift activities. 3. To operate DCS as supervisor & review DCS alarms. 4. Ensure batch charging & other manufacturing operations should be strictly as per BMR/SOP & in line with current GMP practices while working as shift in charge. 5. To maintain manufacturing records online & should comply data integrity practices. 1. To handle shift as shift in charge whenever required. 2. Follow instructions from Manager for the general shift activities. 3. To operate DCS as supervisor & review DCS alarms. 4. Ensure batch charging & other manufacturing operations should be strictly as per BMR/SOP & in line with current GMP practices while working as shift in charge. 5. To maintain manufacturing records online & should comply data integrity practices. 6. To take out sample of intermediate/in-process material and send to IPQC/QC lab. 7. To enter and ensure the production related inputs in SAP system. 8. To be check and ensure the PISCADA reports generation. 9. Transfer finished goods through “Finished Goods Transfer Note”. 10. To Check and ensure minimum stock of consumables, Log books & status labels. 11. Ensuring preventive maintenance of all equipment as per schedule. 12. Co-ordinate with service departments (QA, QC, stores, E & M) for various production related activities. 13. If any major abnormality found in production area / activities, authorized to stop activity immediately & inform to superiors/production Manager. 14. Responsible to maintain housekeeping in plant & take care the cleanliness of equipment. 15. Follow safety instructions/procedures & ensure use of safety outfit while on works. 16. To attend GMP & safety trainings & implement the trainings outcome at workplace. 17. To conduct training to all staff as trainer. 18. Should be aware of the location of firefighting equipment and should know the operation. 19. Report any incident, near miss in my safe portal. 20. Rectify all safety and GMP related observations. 21. He should not leave the work spot unattended and go away without prior permission from Manager. 22. Responsible for allotment of work to operators & casuals. 23. To involve in other initiatives such as AET & CSR. 24. Responsible to carry out the work of his senior in the absence of senior or authorization from senior. 25. To prepare and perform operational and performance qualification protocol. 26. Preparation of SOP’s, BMR, Protocol, Records etc. 27. He should handle DocuSign, ensure, track wise activities. He should handle all QMS activities. Chemical Engineering

Responsibilities

The role involves supervising API production shifts, operating DCS systems, and ensuring all manufacturing operations strictly follow BMR/SOP and GMP guidelines. Responsibilities include maintaining online records, coordinating with QA/QC departments, and managing equipment maintenance and safety protocols.