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Sun Pharma Sr Executive – Production QMS Job 2026 in Dadra

PC Pharma Career Updates Editorial Team · Sep 21, 2026 · 5 min read

Sun Pharma Sr Executive – Production QMS Job 2026 in Dadra

Published on: September 21, 2026

Sun Pharmaceutical Industries Ltd has listed a Sr Executive – Production QMS position at Dadra 1 – Operations Block A.

The role is for experienced pharmaceutical professionals with a background in Production/QMS and regulated OSD manufacturing. Candidates with B.Pharm or M.Pharm and 6–10 years of relevant experience can check the vacancy.

The company has also mentioned exposure to USFDA audits and international regulatory inspections as preferred experience.

1. Sun Pharma Sr Executive – Production QMS Job Details

Particular Details
Company Sun Pharmaceutical Industries Ltd
Position Sr Executive – Production QMS
Location Dadra 1 – Operations Block A
Qualification B.Pharm / M.Pharm
Experience 6–10 years
Functional Area Production / QMS
Manufacturing Area Regulated OSD manufacturing
Preferred Exposure USFDA audits and international regulatory inspections
Posted September 16, 2026
Salary Not disclosed
Official Job Listing / Apply Online View Sun Pharma Vacancy

2. About the Role

This position brings together production operations and Quality Management System (QMS) activities.

The selected candidate will work on production documentation, batch monitoring, deviations, investigations, CAPA, change controls and compliance-related activities. The role also involves coordination with QA during manufacturing operations.

Since the vacancy specifically asks for experience in regulated OSD manufacturing, candidates should have practical exposure to areas such as granulation, compression, coating or packing.

3. Key Responsibilities

According to the job description, the role includes:

  • Preparing, reviewing and maintaining SOPs, BMRs and other production documents
  • Monitoring batch manufacturing activities
  • Coordinating with QA for line clearance and in-process checks
  • Initiating and investigating production deviations
  • Preparing investigation reports and implementing CAPA
  • Handling change controls and QMS activities
  • Conducting training for production staff on cGMP, SOPs and QMS requirements
  • Supporting audit and inspection readiness
  • Working on root-cause analysis and process improvement
  • Supporting data integrity and electronic documentation practices

4. OSD Manufacturing Experience

The vacancy specifically mentions experience in OSD manufacturing.

Relevant experience can include:

Manufacturing Area Relevant Experience
Granulation Experience with granulation operations
Compression Tablet compression activities
Coating Tablet coating processes
Packing Pharmaceutical packing operations
Batch Documentation BMR and production records
In-process Activities Line clearance and in-process checks

Candidates should relate these areas to their actual experience rather than simply adding keywords to their resumes.

5. QMS Experience

The position also has a strong QMS component. Experience with production documentation and quality-related investigations can therefore be relevant.

Areas mentioned in the vacancy include:

  • SOP preparation and review
  • Batch manufacturing records
  • Deviations and investigations
  • CAPA
  • Change controls
  • Root-cause analysis
  • Training and compliance
  • Audit and inspection readiness
  • Data integrity

Professionals interested in broader QA career paths can also read Career in Quality Assurance (QA) After B.Pharm.

6. Regulatory and Compliance Exposure

Sun Pharma mentions cGMP, USFDA guidelines and other regulatory requirements as part of the role.

Exposure to USFDA audits and international regulatory inspections is preferred.

This makes previous experience with regulated manufacturing environments, compliance documentation and inspection-related activities particularly relevant to the position.

For readers interested in regulatory and compliance careers, the Regulatory Compliance Analyst Job article covers a different type of compliance-focused opportunity.

7. Qualification and Experience

The official vacancy specifies:

Requirement Details
Education B.Pharm / M.Pharm in Pharmaceutical Sciences
Experience 6–10 years
Manufacturing Experience Production/QMS in regulated OSD manufacturing
Regulatory Exposure USFDA and international inspections preferred

The experience requirement is specifically connected to Production/QMS in regulated OSD manufacturing.

8. What to Highlight in Your Resume

If your experience matches the vacancy, make the relevant responsibilities easy for the recruiter to find.

Depending on your actual work, these may include:

OSD manufacturing • BMR • SOPs • Deviations • CAPA • Change Control • cGMP • USFDA • Investigations • QA coordination • Audit/Inspection support

Avoid adding skills or regulatory experience that you have not actually worked with.

9. How to Apply

Candidates interested in the position can apply through the official Sun Pharma careers portal.

Apply for Sr Executive – Production QMS at Sun Pharma

Before applying, review the official vacancy page to confirm the latest application status, eligibility requirements and other job details.

10. Is This Job Suitable for Freshers?

No. The official vacancy specifies 6–10 years of experience in Production/QMS in regulated OSD manufacturing.

Therefore, this particular position is intended for experienced professionals rather than fresh graduates.

11. Related Pharmaceutical Jobs

If you are exploring other pharmaceutical production, quality and career opportunities, you can also check:

12. Frequently Asked Questions

What is the qualification for the Sun Pharma Sr Executive – Production QMS job?

Candidates should have a B.Pharm or M.Pharm in Pharmaceutical Sciences.

How much experience is required?

The official requirement is 6–10 years of experience in Production/QMS in regulated OSD manufacturing.

Is OSD manufacturing experience required?

Yes. The job description specifically mentions experience in regulated OSD manufacturing.

Is USFDA experience mandatory?

Sun Pharma lists exposure to USFDA audits and international regulatory inspections as preferred. The listing does not state it as a mandatory requirement.

Is the salary mentioned?

No salary information is provided in the official vacancy listing.

Where is the position located?

The position is based at Dadra 1 – Operations Block A.

Where should candidates apply?

Applications should be submitted through the official Sun Pharma careers portal. Apply for Sr Executive – Production QMS at Sun Pharma

13. Important Note

Job openings can change or close without notice. Candidates should check the official company vacancy before applying and should not make any payment to anyone claiming to offer the job.

PharmaCareerUpdates.com is an independent career-information website and is not affiliated with Sun Pharmaceutical Industries Ltd.

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Pharma Career Updates Editorial Team

Tracks exam notifications, recruitment drives and industry news across India's pharmacy sector.

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