Indus Pharma Recruitment – Regulatory Affairs, QA, QC & Engineering Jobs in Neemrana for Experienced Professionals
Indus Pharma Recruitment – Regulatory Affairs, QA, QC & Engineering Jobs in Neemrana
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(Indus Pharma Recruitment – RA, QA, QC & Engineering Jobs) |
Introduction
Indus Pharma Pvt. Ltd. has announced multiple pharmaceutical job openings at its Neemrana, Rajasthan facility for experienced professionals across Regulatory Affairs, Quality Assurance (QA), Quality Control (QC), and Engineering departments. These opportunities are designed for candidates who want to advance their careers in pharmaceutical manufacturing, compliance, quality systems, analytical testing, regulatory documentation, and engineering operations.
Professionals with experience ranging from 2 to 7 years can explore these openings based on their technical expertise and departmental background. Candidates possessing qualifications such as B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, B.Tech, Diploma, or ITI may be eligible depending on the role.
About Indus Pharma Pvt. Ltd.
Indus Pharma Pvt. Ltd. is an Indian pharmaceutical manufacturing company engaged in the development and production of quality pharmaceutical products. The company operates manufacturing facilities that support regulated pharmaceutical operations while maintaining quality, compliance, and operational excellence.
The company focuses on pharmaceutical manufacturing, quality management systems, regulatory compliance, laboratory operations, and engineering infrastructure to support safe and effective healthcare products.
Company Name: Indus Pharma Pvt. Ltd.
Industry: Pharmaceutical Manufacturing
Headquarters: India
Work Location: Neemrana, Rajasthan
Business Area: Pharmaceutical Manufacturing and Regulatory Operations
Job Overview Summary
Indus Pharma is currently recruiting experienced professionals for multiple departments including Regulatory Affairs, Quality Assurance, Quality Control, and Engineering.
These positions provide opportunities to work in GMP-regulated environments and contribute to critical pharmaceutical functions such as dossier compilation, laboratory quality assurance, HPLC analysis, and HVAC operations.
Candidates should carefully review the department-specific requirements before applying.
Vacancy Details
| Department | Position | Experience |
|---|---|---|
| Regulatory Affairs | Sr. Executive | 6–7 Years |
| Quality Assurance | Lab QA | 3–4 Years |
| Quality Control | HPLC | 4–5 Years |
| Engineering | HVAC | 2–3 Years |
Company: Indus Pharma Pvt. Ltd.
Location: Neemrana, Rajasthan
Employment Type: Full-Time
Industry: Pharmaceutical Manufacturing
Regulatory Affairs – Sr. Executive
Experience Required
6–7 Years
Key Responsibilities
The Regulatory Affairs professional will primarily focus on pharmaceutical dossier compilation and regulatory documentation management.
Responsibilities include:
- End-to-end dossier compilation activities.
- Preparation of regulatory submissions.
- Review of regulatory documents.
- Coordination of submission-related documentation.
- Regulatory record maintenance.
- Compliance with internal and external regulatory requirements.
- Supporting pharmaceutical registration activities.
Quality Assurance – Lab QA
Experience Required
3–4 Years
Key Responsibilities
Candidates selected for Lab QA will support pharmaceutical quality systems and laboratory compliance activities.
Responsibilities include:
- Reviewing laboratory documentation.
- Supporting GMP compliance.
- Monitoring laboratory quality systems.
- Reviewing analytical records.
- Managing quality documentation.
- Supporting internal quality audits.
- Ensuring adherence to approved procedures.
Quality Control – HPLC
Experience Required
4–5 Years
Key Responsibilities
The Quality Control professional will perform pharmaceutical analytical testing and laboratory activities.
Responsibilities include:
- HPLC operation and analysis.
- Routine pharmaceutical testing.
- Documentation of analytical results.
- Compliance with laboratory SOPs.
- Maintaining GLP standards.
- Supporting batch release testing activities.
- Handling analytical instruments and reports.
Engineering – HVAC
Experience Required
2–3 Years
Key Responsibilities
Engineering professionals will support pharmaceutical utility operations and HVAC systems.
Responsibilities include:
- HVAC system operation.
- Preventive maintenance activities.
- Equipment monitoring.
- Troubleshooting HVAC issues.
- Maintaining engineering records.
- Ensuring uninterrupted facility operations.
- Compliance with pharmaceutical engineering standards.
Eligibility Criteria
Candidates possessing any of the following qualifications may be considered depending on the department:
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc
- M.Sc
- B.Tech
- Diploma
- ITI
Experience Requirements
- Engineering HVAC: 2–3 Years
- Quality Assurance Lab QA: 3–4 Years
- Quality Control HPLC: 4–5 Years
- Regulatory Affairs Sr. Executive: 6–7 Years
These openings are intended primarily for experienced pharmaceutical professionals.
Skills Required
Depending on the selected department, candidates should possess knowledge of:
- Regulatory Dossier Compilation
- Regulatory Documentation
- GMP Compliance
- Quality Management Systems
- Laboratory Documentation
- HPLC Analysis
- Pharmaceutical Analytical Testing
- GLP Requirements
- HVAC Operations
- HVAC Maintenance
- Pharmaceutical Manufacturing Processes
- SOP Compliance
- Technical Documentation
- Quality Systems
- Pharmaceutical Regulatory Affairs
Salary Estimate
Indus Pharma has not officially disclosed salary details for these positions.
Based on current pharmaceutical industry trends, approximate salary ranges may be:
- Engineering HVAC: ₹3.5 – ₹5.5 LPA
- QA Lab QA: ₹4.5 – ₹7 LPA
- QC HPLC: ₹5 – ₹8 LPA
- Regulatory Affairs Sr. Executive: ₹8 – ₹14 LPA
Actual compensation may vary depending on experience, technical expertise, interview performance, and company policies.
Interview Details
The company has not officially announced interview dates or selection schedules.
Shortlisted candidates may be contacted directly by the HR team after CV screening for further evaluation rounds, technical interviews, and final discussions.
Required Documents
Applicants should keep the following documents ready:
- Updated Resume/CV
- Educational Certificates
- Experience Certificates
- Current Salary Details (if applicable)
- Latest Increment Letter
- Identity Proof
- Passport Size Photograph
- Previous Employment Documents
- Technical Training Certificates (if available)
Job Location
SVP Plant
Neemrana, Rajasthan, India
Candidates should be willing to work from the Neemrana manufacturing facility.
How to Apply
Interested candidates can send their updated CV to:
Email: hr@induspharmaindia.com
Applicants should mention the department and position name clearly in the email subject line.
Example:
Application for QC HPLC Position
or
Application for Regulatory Affairs Sr. Executive
Frequently Asked Questions (FAQs)
1. Is this opportunity suitable for freshers?
No. These openings are intended for experienced professionals with 2–7 years of relevant pharmaceutical industry experience.
2. Which department has the highest experience requirement?
The Regulatory Affairs Sr. Executive role requires approximately 6–7 years of experience.
3. Are B.Pharm and M.Pharm candidates eligible?
Yes. Depending on the department and relevant experience, B.Pharm and M.Pharm candidates may apply.
4. Is HPLC experience mandatory for the QC role?
Yes. Practical experience in HPLC analysis is one of the key requirements for the Quality Control position.
5. Is the Engineering role related to pharmaceutical HVAC systems?
Yes. Candidates should have experience handling HVAC systems used in pharmaceutical manufacturing facilities.
6. What is the job location?
The positions are based at Indus Pharma's Neemrana facility in Rajasthan.
7. How can I apply?
Candidates can apply by sending their updated resume to hr@induspharmaindia.com.
Final Conclusion
Indus Pharma's latest recruitment drive offers excellent opportunities for experienced pharmaceutical professionals across Regulatory Affairs, Quality Assurance, Quality Control, and Engineering functions. Candidates with expertise in dossier compilation, laboratory quality systems, HPLC analysis, and HVAC operations can find strong career growth opportunities within a GMP-regulated pharmaceutical manufacturing environment.
Interested professionals should review the eligibility requirements carefully and submit their updated resumes at the earliest for consideration.
Disclaimer
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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