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JAMP India Pharmaceuticals Pvt. Ltd. is conducting a Walk-In Interview for experienced Quality Assurance professionals. Candidates with relevant pharmaceutical manufacturing experience and qualifications in M.Pharm, B.Pharm, or M.Sc are invited to attend the interview for multiple Quality Assurance functions.
Interview Date & Time
- Interview Date: Sunday, 28 June 2026
- Time: 10:00 AM to 4:00 PM
About JAMP India Pharmaceuticals Pvt. Ltd.
JAMP India Pharmaceuticals Pvt. Ltd. is a part of the JAMP Pharma Group, a Canadian pharmaceutical company. The organization focuses on delivering high-quality pharmaceutical products while maintaining international quality and regulatory standards.
Open Positions
1. Quality Assurance β Stability (3 Positions)
Position:
- Senior Executive
- Executive
Qualification:
- M.Pharm
- B.Pharm
- M.Sc
Experience:
- 3β7 Years
Key Responsibilities:
- Manage and maintain stability documentation and protocols.
- Analyze stability data and recommend shelf-life updates.
- Handle change control impact assessments.
- Review laboratory test results and investigate OOS/OOT findings.
- Coordinate ongoing stability programs and annual reports.
- Work closely with QA, QC, Regulatory, and external stakeholders while ensuring GMP compliance.
2. Quality Assurance β Commercial Release & Support (4 Positions)
Position:
- Senior Executive
- Executive
- Senior Officer
Qualification:
- M.Pharm
- B.Pharm
Experience:
- 4β8 Years
Market:
- Regulated Market
Dosage Forms:
- Oral Solid
- Parenteral
- Ophthalmic Solution
- Biosimilars
Key Responsibilities:
- Review Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), COA, Specifications, and STP.
- Review QMS documents including Deviations, OOS, Incidents, Investigations, and Change Controls.
- Coordinate with cross-functional teams for commercial batch release.
- Collaborate with CMOs for smooth product release.
3. Quality Assurance β Operations (3 Positions)
Position:
- Assistant Manager
- Senior Executive
Qualification:
- M.Pharm
- B.Pharm
Experience:
- 8β10 Years
Market:
- Regulated Market
Dosage Forms:
- Oral Solid
- Parenteral
- Ophthalmic Solution
- Biosimilars
Key Responsibilities:
- Support QA activities for new product launches across Canada and other markets.
- Review regulatory dossiers for GMP compliance.
- Prepare due diligence reports and coordinate with cross-functional teams.
- Manage commercial batch release with CMOs.
- Review manufacturing, analytical, and QMS documentation as per regulatory expectations.
Qualification
- M.Pharm
- B.Pharm
- M.Sc (Applicable for Stability role)
Experience Required
- 3 to 10 Years (Depending on the position)
Department
- Quality Assurance β Stability
- Quality Assurance β Commercial Release & Support
- Quality Assurance β Operations
Venue Address
JAMP India Pharmaceuticals Pvt. Ltd.
A-1207, 12th Floor, Navratna Corporate Park,
Ambli Bopal Road, Ambli, Ahmedabad β 380058
Documents to Carry
- Updated Resume
- Passport Size Photograph
- Last Three Months Salary Slips
- Appointment Letter
Important Notes
- Candidates interviewed within the last 30 days are not eligible to apply.
- The company does not recruit through consultants or agents demanding money for interviews or jobs.
- Candidates unable to attend the walk-in interview may send their updated resume to hrindia@jamppharma.com or apply through the QR code provided in the official notification.
Frequently Asked Questions (FAQs)
1. Who can attend this walk-in interview?
Candidates with 3β10 years of pharmaceutical Quality Assurance experience and the required qualifications can attend.
2. Which departments are hiring?
Quality Assurance β Stability, Commercial Release & Support, and Operations.
3. What qualifications are required?
M.Pharm, B.Pharm, and M.Sc (for selected roles).
4. What documents should candidates carry?
Updated resume, passport-size photograph, last three months’ salary slips, and appointment letter.
5. Can candidates who cannot attend the walk-in still apply?
Yes. Candidates may send their updated resume to hrindia@jamppharma.com as mentioned in the official notification.
