Jobs in Sidcul

Production & QA Documentation Executive (Urgent Requirement)

Website GNPAL Speciality Molecules LLP

Job Overview
GNPAL Speciality Molecules LLP has an urgent requirement and is actively hiring experienced professionals to manage Production & QA Documents. We are looking for dedicated individuals to join our operations in Sitarganj, Uttarakhand.

This is a critical role within our manufacturing and quality assurance framework. Candidates who are available to join immediately will be highly preferred for this position.

Key Job Details
Required Experience: 05+ Years of relevant industry experience.
Salary / Compensation: ₹3.5 Lakhs to ₹4.5 Lakhs LPA (CTC).
Joining Availability: Immediate joiners are preferred.

Job Profile & Key Responsibilities
The selected candidate will be responsible for overseeing crucial documentation processes to ensure compliance and operational excellence. The day-to-day responsibilities include:

Handling all core Production and Quality Assurance (QA) documentation activities.
The preparation, thorough review, and ongoing maintenance of BMR (Batch Manufacturing Records), BPR (Batch Production Records), SOPs (Standard Operating Procedures), logbooks, and other vital records.
Seamless coordination with both the Production and QA departments to ensure strict documentation compliance across the board.
Ensuring the strict implementation of proper Good Documentation Practices (GDP) and current Good Manufacturing Practices (cGMP).
Providing essential support during internal and external audits, including comprehensive documentation verification.
Maintaining meticulous document control and secure record management systems.
Working closely and collaboratively with the Production and QA teams to guarantee the accuracy, completeness, and timely execution of all documentation.

Required Skills & Qualifications
To be successful in this role, the ideal candidate must possess a strong foundation in pharmaceutical or chemical manufacturing quality standards.

The candidate should have in-depth and practical knowledge of cGMP (current Good Manufacturing Practices).
Thorough understanding of GDP (Good Documentation Practices) guidelines and standard industry documentation practices is mandatory.

How to Apply
Interested candidates who meet the above experience and skill requirements are encouraged to share their updated resumes immediately.

Email your updated resume to: hr@gnpalspecialitymolecules.com
Contact via Mobile: +91 9193007878

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