Apprentice

Piramal Pharma Ltd; Mahad; On-site; INR 134,000 - 167,000; Full time

Job summary

Piramal Pharma Solutions invites applications for an Apprentice to support production operations. The role involves machine setting, changeovers, and ensuring production meets quality and time targets while adhering to cGMP norms.

You will help maintain clean, safe production areas and assist in QEHS-related activities. Candidates should be Science graduates or D.Pharm holders, capable of training junior staff and participating in continuous improvement initiatives within the site.

Qualifications

• Familiarity with cGMP norms.
• Ability to maintain department cleanliness and organize workload.

Responsibilities

• Machine setting and changeover to ensure production flow.
• Maintain department cleanliness and hygiene per standards.
• Train subordinates and ensure proper PPE use.
• Identify QEHS issues and monitor corrective actions.
• Prepare and review departmental batch records and related documentation.

Education

Science graduate / D.Pharm

Job description

Division Piramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia. This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide. For more details, please visit : www.piramalpharmasolutions.com

Job Title

Apprentice

Job Description

• Machine setting. 2. Machine change over. 3. To do departmental activities as per cGMP norms. 4. To give optimum productivity with subsequent improvement in it as per need, within specified time and quality by effective utilization of available resources so as to deliver the product as per market requirement. 5. To maintain department cleanliness. 6. To train subordinates. 7. To determine internal and external QEHS issues as well as needs and expectations of relevant interested parties and monitor the same. 8. To implement QEHS policy & objectives. 9. Ensure use of PPE. 10. To identify hazards & risk of defined process and control on it (Unsafe condition / Reporting of near miss, accidents) 11. To identify & communicate incidents QEHS non conformities, investigate and take corrective actions on the same. 12. To ensure work permit system during maintenance. 13. To participate and consult EHS activities to promote the EHS culture in the organization. 14. To implement QEHS continual improvement projects at site and monitor. 15. Responsible for providing quality product and maintaining quality system of company. 16. To avoid of breach of data integrity at all the levels. 17. Do proper sanitation activities at all the levels. 18. Cross verification of Raw Material and packing material. 19. Daily Verification of weighing balance. 20. Update door status label of area, Weight, label & record the weight of blended powder in BMR. 21. Follow gowning procedure and use proper PPEs before entering into production areas. 22. Write online Batch Manufacturing Record. And coordinate to prepare and review departmental documents. 23. Switch off area tube lights and other utilities when it is not required. 24. Keep the door closed of production areas. Science graduate / D.Pharm