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Quality Assurance Jobs in Nagpur – Unijules Life Sciences Ltd.
Published on: September 18, 2026
Unijules Life Sciences Ltd. is hiring for a Quality Assurance position in Nagpur, Maharashtra. The opportunity is intended for experienced pharmaceutical professionals with a B.Pharm (Bachelor of Pharmacy) or M.Pharm (Master of Pharmacy) qualification and 4–5 years of pharmaceutical industry experience.
Experience in liquid or solid dosage manufacturing is preferred for this role.
1. Unijules Life Sciences QA Vacancy – Job Overview
| Particular | Details |
|---|---|
| Company | Unijules Life Sciences Ltd. |
| Position | Quality Assurance |
| Location | Nagpur, Maharashtra |
| Qualification | B.Pharm / M.Pharm |
| Experience | 4–5 years |
| Industry | Pharmaceutical |
| Remuneration | Best in Industry |
| Preferred Experience | Liquid or solid dosage manufacturing |
| Job Area | Quality Assurance |
2. About the Quality Assurance Role
The position involves supporting quality activities within a pharmaceutical manufacturing environment.
The selected professional may work across areas such as:
- cGMP compliance
- Pharmaceutical audits
- Quality documentation
- Validation
- Stability activities
- Vendor approval
- Quality-system requirements
- QA personnel training
Because this is an experienced-level position, practical knowledge of pharmaceutical manufacturing and QA procedures is important.
3. Key Responsibilities
The responsibilities mentioned for the position cover several parts of pharmaceutical quality management.
| Area | Key Work |
|---|---|
| Audits | Conduct audits within the pharmaceutical manufacturing plant |
| cGMP | Implement and maintain current Good Manufacturing Practices |
| QA Operations | Monitor day-to-day Quality Assurance activities |
| Training | Train QA personnel on applicable procedures and requirements |
| Documentation | Prepare, review and maintain quality-related documents and SOPs |
| Validation | Prepare/review protocols and support process and equipment validation |
| Stability | Handle stability-related protocols and documentation |
| Annual Product Review | Prepare and review APRs |
| Vendor Approval | Manage approval activities for raw-material and packaging-material vendors |
| Compliance | Monitor adherence to established quality procedures |
The role therefore covers multiple QA functions rather than being limited to routine documentation or in-process checks.
4. Educational Qualification
The vacancy lists the following qualifications:
| Qualification | Full Form |
|---|---|
| B.Pharm | Bachelor of Pharmacy |
| M.Pharm | Master of Pharmacy |
The qualification should be supported by the relevant pharmaceutical industry experience required for the position.
5. Experience Required
The vacancy specifies 4–5 years of pharmaceutical industry experience.
Experience in liquid or solid dosage manufacturing plants is preferred.
| Experience Area | Relevance to the Role |
|---|---|
| Pharmaceutical QA | Core requirement |
| Liquid Dosage Manufacturing | Preferred |
| Solid Dosage Manufacturing | Preferred |
| Audits | Relevant |
| Validation | Relevant |
| cGMP | Relevant |
| Quality Documentation | Relevant |
| Stability | Relevant |
| Vendor Qualification | Relevant |
Candidates should compare their actual responsibilities with the vacancy rather than relying only on their job title.
6. Skills Relevant to This Position
For an experienced QA professional, the following areas are particularly relevant:
| Skill / Knowledge | Where It May Be Used |
|---|---|
| cGMP | Manufacturing and quality compliance |
| Audits | Internal and pharmaceutical quality audits |
| SOPs | Preparation, review and implementation |
| Process Validation | Validation of manufacturing processes |
| Equipment Validation | Qualification and validation activities |
| Stability | Stability protocols and documentation |
| Annual Product Review | Review of product quality and manufacturing data |
| Vendor Qualification | Approval of raw-material and packaging-material suppliers |
| QA Training | Training QA personnel |
| Documentation | Maintaining quality-system records |
Strong documentation and communication skills are also useful because the position involves reviewing records, procedures and quality-related activities.
7. Who Can Consider Applying?
This vacancy may be relevant to professionals who meet the stated qualification and experience requirements, particularly:
- B.Pharm professionals with relevant industry experience
- M.Pharm professionals
- QA Officers and QA Executives
- Pharmaceutical QA professionals
- Candidates with liquid dosage manufacturing experience
- Candidates with solid dosage manufacturing experience
If you want to understand the QA career path in more detail, you can also read our guide on Career in Quality Assurance (QA) After B.Pharm, which covers common QA roles, skills and career scope.
8. How to Prepare Your Resume
For an experienced QA position, avoid sending a generic resume that only lists your designation.
Your CV should clearly show the actual QA activities you have handled.
| Resume Section | What to Highlight |
|---|---|
| QA Experience | Specific pharmaceutical QA responsibilities |
| Manufacturing Exposure | Liquid or solid dosage manufacturing |
| Compliance | cGMP and quality-system activities |
| Audits | Audit participation or handling |
| Validation | Process and equipment validation |
| Documentation | SOPs, protocols and quality records |
| Stability | Stability-related responsibilities |
| Vendor Management | Vendor qualification or approval |
| Training | QA personnel training experience |
Avoid adding technical terms simply because they appear in the job description. You should be able to explain anything listed on your CV during an interview.
9. Documents to Keep Ready
Before applying, candidates should have the following information ready:
| Document / Information | Purpose |
|---|---|
| Updated CV/Resume | Shows qualification and relevant experience |
| Educational Details | B.Pharm/M.Pharm qualification information |
| Employment Details | Previous pharmaceutical industry experience |
| QA Experience Details | Specific responsibilities handled |
| Contact Information | Phone number and email for recruitment communication |
Make sure the information in the CV is accurate and consistent with your actual experience.
10. How to Apply
Interested and eligible candidates can send their updated resume to:
Email: hrd@unijules.com
Candidates should mention “Quality Assurance” in the email subject line and attach an updated CV highlighting relevant pharmaceutical QA experience.
Official Careers Page
Unijules Life Sciences – Careers
Before applying, verify that the vacancy is still active and check the latest application instructions through the company’s official source.
11. External Resources for QA Professionals
Candidates who want to strengthen their understanding of pharmaceutical quality requirements can refer to authoritative resources such as:
- FDA – Current Good Manufacturing Practice (cGMP)
- CDSCO – Central Drugs Standard Control Organisation
These resources are for general learning and are not part of the Unijules recruitment process.
12. More QA/QC Jobs
Looking for other pharmaceutical quality opportunities? Explore our QA/QC Jobs section for additional QA and QC vacancies.
13. Frequently Asked Questions
What position is available at Unijules Life Sciences?
The vacancy is for a Quality Assurance position in Nagpur.
What qualification is required?
The vacancy lists B.Pharm (Bachelor of Pharmacy) or M.Pharm (Master of Pharmacy).
How much experience is required?
Candidates should have 4–5 years of pharmaceutical industry experience.
Is manufacturing experience preferred?
Yes. Experience in liquid or solid dosage manufacturing plants is preferred.
What salary is offered?
The vacancy mentions “Best in Industry” remuneration. A specific salary amount has not been disclosed.
How can I apply?
Eligible candidates can send their updated resume to hrd@unijules.com with “Quality Assurance” in the email subject line.
Where is the job located?
The position is based in Nagpur, Maharashtra.
14. Important Note
This article is provided for career-information purposes. PharmaCareerUpdates.com is an independent career-information website and is not affiliated with Unijules Life Sciences Ltd.
Candidates should verify the current vacancy status, eligibility requirements and application instructions through the company’s official recruitment source before applying.
