JAMP India Pharmaceuticals Pvt. Ltd. is conducting a Walk-In Interview for Quality Assurance professionals in Ahmedabad. Candidates with experience in Stability, Commercial Release & Support, and QA Operations are invited to attend. This is an excellent opportunity for pharmaceutical professionals looking to build their careers in a regulated market environment involving oral solids, parenterals, ophthalmic solutions, and biosimilars.
Walk-In Interview Details
Company: JAMP India Pharmaceuticals Pvt. Ltd.
Department: Quality Assurance
Location: A-1207, 12th Floor, Navratna Corporate Park, Ambli Bopal Road, Ambli, Ahmedabad – 380058
Interview Date: 28 June
Time: 10:00 AM to 4:00 PM
Vacancy Details
Quality Assurance – Stability (3 Positions)
Designation: Senior Executive / Executive
Qualification:
- M.Pharm
- B.Pharm
- M.Sc
Experience Required: 3 to 7 Years
Key Responsibilities
- Manage and maintain stability documentation, protocols, and product shelf-life records.
- Develop and review stability protocols.
- Analyze stability data and recommend shelf-life updates.
- Assess change controls for potential impact on product stability.
- Review laboratory test results and investigate OOS/OOT findings.
- Prepare non-conformity reports and annual stability review reports.
- Coordinate with QA, QC, Regulatory Affairs, CMOs, and suppliers.
- Ensure compliance with GMP requirements.
Quality Assurance – Commercial Release & Support (4 Positions)
Designation: Senior Executive / Executive / Senior Officer
Qualification:
- M.Pharm
- B.Pharm
Experience Required: 4 to 8 Years
Market Exposure: Regulated Markets
Dosage Forms:
- Oral Solid Dosage Forms
- Parenterals
- Ophthalmic Solutions
- Biosimilars
Key Responsibilities
- Review Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR).
- Review Certificates of Analysis (COA), specifications, and STP documents.
- Evaluate deviations, OOS, incidents, investigations, and change controls.
- Coordinate with cross-functional departments for batch release activities.
- Collaborate with Contract Manufacturing Organizations (CMOs) for smooth commercial operations.
Quality Assurance – Operations (3 Positions)
Designation: Assistant Manager / Senior Executive
Qualification:
- M.Pharm
- B.Pharm
Experience Required: 8 to 10 Years
Market Exposure: Regulated Markets
Dosage Forms:
- Oral Solids
- Parenterals
- Ophthalmic Solutions
- Biosimilars
Key Responsibilities
- Support QA activities for new product launches in Canada and other international markets.
- Review pre-submission dossiers to ensure GMP and regulatory compliance.
- Prepare due diligence reports and coordinate with cross-functional teams.
- Manage commercial batch release activities with CMOs.
- Review manufacturing, analytical, and QMS documentation as per regulatory expectations.
Documents Required for Interview
Candidates should carry the following documents:
- Updated Resume/CV
- Passport Size Photograph
- Last Three Months Salary Slips
- Current Appointment Letter
Important Instructions
- Candidates interviewed within the last 30 days are not eligible to apply again.
- JAMP India Pharmaceuticals Pvt. Ltd. does not charge any registration or placement fee.
- Beware of fraudulent job offers from unauthorized consultants or agents.
- Candidates unable to attend the walk-in interview may submit their updated resume through the official application process mentioned by the company.
Why Join JAMP India Pharmaceuticals?
JAMP India offers opportunities to work in highly regulated pharmaceutical markets with exposure to commercial release, quality systems, stability programs, regulatory compliance, biosimilars, and global pharmaceutical operations. Professionals can gain valuable experience in GMP-compliant manufacturing and quality assurance systems while contributing to international healthcare products.




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