Sr Executive - Production QMS

sun pharma industries

6 - 10 years

10 - 11 Lacs

dadra & nagar haveli nagar

Posted:1 week ago| Platform:

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Skills Required

product quality osd usfda pharma process improvement packaging regulatory compliance continuous improvement monitoring mhra

Work Mode

Work from Office

Job Type

Full Time

Job Description

Job Purpose:

To ensure compliance with cGMP, USFDA, and other regulatory requirements by implementing and maintaining Quality Management System (QMS) practices within the Production department. Responsible for documentation, deviation handling, and continuous improvement initiatives to maintain product quality and regulatory compliance.

Key Responsibilities:

QMS Compliance Documentation
- Prepare, review, and maintain SOPs, Batch Manufacturing Records (BMR), and related production documents.
- Ensure timely closure of deviations, change controls, and CAPAs related to production activities.
- Maintain compliance with USFDA, MHRA, and other global regulatory standards.
Batch Execution Monitoring
- Monitor batch manufacturing processes to ensure adherence to approved procedures.
- Coordinate with QA for line clearance and in-process checks.
Deviation Investigation Handling
- Initiate and investigate production-related deviations.
- Prepare investigation reports and implement corrective and preventive actions.
Training Compliance
- Conduct training for production staff on cGMP, SOPs, and QMS requirements.
- Ensure readiness for regulatory audits and inspections.
Continuous Improvement
- Participate in root cause analysis and process improvement initiatives.
- Support implementation of data integrity practices and electronic documentation systems.

Key Skills Competencies:

Strong knowledge of
cGMP
,
USFDA guidelines
, and regulatory compliance.
Experience in
OSD manufacturing processes
(granulation, compression, coating, packing).
Good documentation and analytical skills.
Ability to handle audits and regulatory inspections.

Qualification Experience:

B.Pharm / M.Pharm
in Pharmaceutical Sciences.
6-10 years
of experience in Production/QMS in a regulated OSD manufacturing environment.
Exposure to
USFDA audits
and other international regulatory inspections preferred.

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