Production QA QC Manufacturing Packing Job in Gujarat at Intas Pharmaceuticals
About the Company
Intas Pharmaceuticals is one of Indiaโs fastest-growing multinational pharmaceutical organizations, with operations in more than 85 countries. Known for its strong focus on quality, compliance, and innovation, Intas manufactures a wide range of formulations including OSD, injectables, and specialty products for regulated and semi-regulated markets.
The company operates multiple USFDA and MHRA-approved manufacturing facilities and offers long-term career growth opportunities for skilled pharmaceutical professionals across production, quality, and manufacturing functions. Production QA QC Manufacturing Packing Job in Gujarat
Job Details
- Company: Intas Pharmaceuticals
- Job Type: Full-time
- Hiring Mode: Walk-In Interview
- Job Location: Ahmedabad, Gujarat
- Departments: Production, Quality Assurance, Quality Control, Manufacturing, Packing
- Experience Required: 3 to 11 Years
- Qualification: M.Sc, B.Pharm, M.Pharm, Diploma, ITI
- Job Status: Verified Job
Walk-In Interview Details
- Interview Date: 11 January 2026 (Sunday)
- Timing: 09:30 AM to 04:30 PM
- Venue:
Pride Plaza Hotel Ahmedabad
Judges Bungalow Road, Off SarkhejโGandhinagar Highway
Bodakdev, Ahmedabad, Gujarat โ 380054
Available Positions & Job Description
1. Technician / Operator
Departments:
- OSD Packing
- Injectable Manufacturing
Experience: 3 to 10 Years
Qualification: ITI / Diploma
Key Responsibilities
- Operate and monitor OSD packing or injectable manufacturing equipment
- Ensure adherence to GMP during production and packing operations
- Perform routine equipment checks and troubleshooting
- Maintain batch records and production documentation
Skills / Qualifications
- ITI or Diploma in relevant technical discipline
- Hands-on experience in pharma production or packing lines
- Knowledge of GMP and shop-floor documentation
Production QA QC Manufacturing Packing Job in Gujarat
2. Senior Executive
Departments:
- Quality Assurance (Doc-Cell, Audit Trail, AQL)
- QA Audit Compliance
- Quality Management System (QMS)
Experience: 6 to 11 Years
Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc
Key Responsibilities
- Handle QA documentation, audit trail review, and data integrity activities
- Conduct IPQA, QMS reviews, and internal audits
- Support regulatory inspections and compliance activities
- Ensure adherence to USFDA and MHRA guidelines
- Review analytical data, validation reports, and environmental monitoring results
Skills / Qualifications
- Strong understanding of regulatory compliance
- Experience in regulated pharmaceutical manufacturing plants
- Knowledge of audit readiness and data integrity requirements
3. Officer / Senior Officer
Department: Quality Control โ Environmental Monitoring
Work Type: Shift-based
Experience: 3 to 6 Years
Qualification: B.Pharm / M.Pharm
Key Responsibilities
- Perform environmental monitoring in sterile and injectable areas
- Conduct microbial analysis and monitoring activities
- Maintain EM records and ensure regulatory compliance
- Support contamination control strategies
Production QA QC Manufacturing Packing Job in Gujarat
Salary & Benefits
- Salary Range: โน3 LPA to โน12 LPA (based on role and experience)
- Technician / Operator: โน3โ6 LPA
- Senior Executive: โน7โ12 LPA
- Performance-based incentives
- Health insurance and statutory benefits
- Exposure to USFDA/MHRA-regulated manufacturing
- Stable long-term career growth in a reputed pharma organization
Why You Should Join Intas Pharmaceuticals
- Work with a globally recognized pharmaceutical company
- Opportunity to work in regulated manufacturing environments
- Strong quality and compliance culture
- Career advancement in production and quality domains
- Employee-centric growth and learning environment
Production QA QC Manufacturing Packing Job in Gujarat
How to Apply
Interested candidates should directly attend the walk-in interview with the following documents: Production QA QC Manufacturing Packing Job in Gujarat
- Updated resume
- Latest salary slips
- Educational and experience certificates
No application fee is required.
Candidates with prior experience in USFDA/MHRA-approved plants will be given preference.

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