Apprentice at Piramal Pharma Ltd

Mahad, maharashtra, India -

Full Time

Start Date

Immediate

Expiry Date

09 Oct, 26

Salary

0.0

Posted On

12 Jul, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Machine Setting, Machine Change Over, cGMP Compliance, QEHS Implementation, PPE Usage, Hazard Identification, Data Integrity, Sanitation, Batch Manufacturing Record, Quality Systems

Industry

Pharmaceutical Manufacturing

Description

Be the First to Apply 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 1. 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 Introduce yourself to our recruiters and we'll get in touch if there's a role that seems like a good match. Piramal Pharma Limited, offers a portfolio of differentiated products and services through its 17 global development and manufacturing facilities and a global distribution network in over 100 countries. PPL includes Piramal Pharma Solutions (PPS), an integrated Contract Development and Manufacturing Organization; Piramal Critical Care (PCC), a Complex Hospital Generics business; and the India Consumer Healthcare business, selling over-the- counter products. In addition, one of PPL’s associate companies, AbbVie Therapeutics India Private Limited is a JV with AbbVie Inc. and has emerged as one of the market leaders in the ophthalmology therapy area. Further, PPL has a minority investment in Yapan Bio Private Limited. In October 2020, PPL received a 20% strategic growth investment from the Carlyle Group. PPL provides equal employment opportunities to all employees and applicants for employment. It prohibits discrimination and harassment based on race, color, age, sex, religion, national origin or ethnicity, disability status, genetics, protected veteran status, sexual orientation, gender identity, or expression, or any other characteristic protected by applicable law. Our employment decisions are based on merit considering qualifications, skills, performance, and achievements. Equal employment opportunity applies to all terms and conditions of employment, including recruitment, selection, training, social programs, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions.

Responsibilities

The role involves machine setting, changeovers, and ensuring production activities adhere to cGMP and QEHS norms. Responsibilities include maintaining cleanliness, documenting Batch Manufacturing Records, and ensuring the delivery of quality products.