Manage documentation, Quality Management Systems (QMS), and validation activities in a pharmaceutical manufacturing setup. Ensure compliance with regulatory standards and support audits and continuous improvement. This is a full-time, in-person role based in Baddi.
Handle documentation related to manufacturing and compliance.
Implement and maintain Quality Management Systems (QMS) as per regulatory requirements.
Coordinate and execute validation activities (process validation, equipment qualification, cleaning validation, etc.).
Ensure adherence to standard operating procedures and maintain proper records for audits and inspections.
Support internal audits and continuous improvement initiatives.
Date Posted:
4th Jul, 2025
Expiration date:
24th Jul, 2026
Location:
Baddi , Himachal Pradesh, India
Job Type:
Full-time
Functional Areas:
Documentation Control
Positions:
1
Job Experience:
0 Year
Salary Period:
Monthly Pay Period
Is Freelance:
No
Nootan Pharmaceuticals
View company profileFounded in:
2010
Location:
Village Tipra, Barotiwala‑Kalka Road (Barotiwala), Tehsil Baddi, District Solan, HP – 174103