Job Overview
GNPal Specialty Molecules LLP is hiring skilled professionals for Production and Quality Assurance (QA) Documentation roles. The ideal candidate should have relevant experience in documentation processes and quality compliance within manufacturing or production environments.

Experience Required
Minimum 5+ years of relevant experience

Salary
₹3.5 – ₹4.5 LPA (CTC)
Compensation based on experience and skills

Joining
Immediate joining preferred

Key Responsibilities
Handle production and QA documentation activities
Prepare, review, and maintain BMR/BPR, SOPs, logbooks, and records
Coordinate with production and QA departments for compliance
Ensure proper GDP and cGMP documentation practices
Support internal and external audits
Maintain document control and record management systems
Collaborate with production and QA teams for accuracy and timely documentation

Required Skills
Knowledge of cGMP and GDP guidelines
Strong documentation and organizational skills
Attention to detail and compliance standards
Ability to work in a team environment

Job Type
Full-time

How to Apply
Send your updated resume to: hr@gnpalspecialitymolecules.com

Contact Information
Mobile: +91 91930 07878

Important Notes
Candidates must have relevant experience in documentation roles
Immediate joiners will be given preference
Only shortlisted candidates will be contacted