Junior Engineer - Equipment Qualification (Pharmaceutical) PQE Group

2.0 - 6.0 years

0 Lacs

rupnagar, punjab

On-site

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia, and the Americas. Following a new opportunity, we are currently looking for a Junior Consultant: Qualification & Validation (CQV) to join our team in an onsite project at Rupnagar (Chandigarh) Location. The ideal candidate should have 2+ years of experience in a similar role and be able to review and update P&ID, prepare Qualification Documents like Validation Plan, Design Qualification, User requirement specification, Installation Quali...

Posted 4 months ago

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Validation Manager Oxera Precision Tech Pvt. Ltd.

5.0 - 9.0 years

0 Lacs

karnataka

On-site

You will be working as a Validation Manager at EVOL ORTHO TECH located in Bengaluru, India. The company is involved in the manufacturing of knee orthopaedic implants for the Indian Market. Established as a greenfield project in 2025, EVOL ORTHO TECH is a Joint-Venture between a French and Mauritius Based Company. As a Validation Manager, you will report to the Quality & Regulatory Affairs General Manager and oversee a team of 3 members after ramp-up. The ideal candidate will hold a BE (MECHANICAL) degree or equivalent qualification. Your primary responsibilities will include managing process monitoring, material analysis tests, preparing qualification and validation files, handling process c...

Posted 4 months ago

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Pharmaceutical Documentation Specialist Papillon Resource Management Private Limited

3.0 - 5.0 years

3 - 5 Lacs

Navi Mumbai

Work from Office

Develop and manage comprehensive pharmaceutical-grade documentation throughout the project lifecycle.Prepare key qualification documents: Design Qualification (DQ), Functional Design Specification (FDS), Hardware Design Specification (HDS). Required Candidate profile • 3-5 years of experience specifically in pharmaceutical documentation or a similar quality/validation role within a regulated industry. • Strong understanding and practical experience with DQ, FDS.

Posted 6 months ago

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Pharmaceutical Documentation Specialist Papillon Resource Management Private Limited

3.0 - 5.0 years

3 - 5 Lacs

Navi Mumbai

Work from Office

Posted 6 months ago

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