Intas Walk-In QA QC Microbiology
Intas Hiring QA QC Microbiology Roles | Ahmedabad
Intas Pharmaceuticals hiring QA, QC and Microbiology roles. B.Pharm, M.Pharm, B.Sc, M.Sc candidates with 2–7 years experience eligible.
Intas Pharmaceuticals Ltd. is conducting a walk-in recruitment drive for experienced professionals at its Matoda manufacturing facility in Ahmedabad, Gujarat. The company is hiring for Quality Assurance, Quality Control, and Microbiology departments, offering opportunities for Officers, Senior Officers, and Executives with experience in regulated pharmaceutical manufacturing environments.
Candidates with qualifications such as B.Pharm, M.Pharm, B.Sc, and M.Sc can attend the walk-in interview scheduled on 21st June 2026. Professionals having hands-on experience in cGMP-compliant facilities, regulatory-approved manufacturing plants, quality systems, analytical review, validation, microbiological testing, and laboratory operations are encouraged to participate.
This recruitment drive presents an excellent opportunity for candidates seeking pharmaceutical quality assurance jobs, quality control analyst careers, microbiology executive positions, validation roles, and regulatory compliance opportunities within a globally recognized pharmaceutical company.
Primary Keyword: Quality Assurance Jobs
Company Overview
Intas Pharmaceuticals Ltd. is one of the world’s leading multinational pharmaceutical formulation development, manufacturing, and marketing companies. The organization has established a strong global footprint and currently operates in more than 85 countries worldwide.
A significant portion of Intas’ revenue comes from highly regulated international markets including the United States and Europe. The company has consistently expanded its operations through investments in pharmaceutical innovation, advanced manufacturing technologies, quality systems, and global regulatory compliance.
Intas is recognized for maintaining world-class manufacturing standards and fostering a culture focused on healthcare innovation, employee development, and operational excellence. Employees gain exposure to international regulatory requirements, advanced pharmaceutical manufacturing practices, and highly regulated market operations.
The Matoda facility is one of the company’s key manufacturing sites supporting global pharmaceutical operations.
Job Role & Responsibilities
Quality Assurance (QMS / Analytical Review / Validation & Qualification / IPQA)
Designation: Officer / Senior Officer / Executive
Qualification: B.Pharm / M.Pharm / M.Sc
Experience: 2–7 Years
Key Responsibilities
- Manage Quality Management System (QMS) activities.
- Perform analytical review and documentation review processes.
- Execute validation and qualification programs.
- Conduct In-Process Quality Assurance (IPQA) activities.
- Review batch manufacturing and packaging records.
- Support deviation investigations and CAPA implementation.
- Participate in regulatory audits and compliance inspections.
- Ensure adherence to cGMP requirements and quality standards.
- Maintain documentation according to data integrity guidelines.
Preferred Expertise
- QMS Management
- IPQA Operations
- Validation & Qualification
- Analytical Review
- Regulatory Compliance
- GMP Documentation
- Audit Readiness
Quality Control
Designation: Senior Officer / Executive
Qualification: B.Sc, M.Sc (Organic Chemistry / Analytical Chemistry), B.Pharm, M.Pharm
Experience: 3–7 Years
Key Responsibilities
- Perform analysis of raw materials, finished products, and stability samples.
- Operate analytical instruments according to laboratory procedures.
- Maintain laboratory documentation and analytical records.
- Support investigation of out-of-specification results.
- Ensure compliance with GMP, GLP, and laboratory safety requirements.
- Participate in method execution and laboratory compliance programs.
Preferred Expertise
- Analytical Testing
- Stability Studies
- Laboratory Compliance
- Regulatory Documentation
- Data Integrity Practices
- cGMP Laboratory Operations
Microbiology
Designation: Senior Officer / Executive
Qualification: B.Sc / M.Sc Microbiology
Experience: 3–7 Years
Key Responsibilities
- Perform microbiological testing activities.
- Support environmental monitoring programs.
- Conduct microbial analysis and laboratory investigations.
- Maintain microbiology laboratory records and documentation.
- Ensure compliance with microbiological quality standards.
- Participate in audit readiness and regulatory inspections.
Preferred Expertise
- Microbiological Testing
- Environmental Monitoring
- Laboratory Documentation
- GMP Compliance
- Regulatory Audit Support
Eligibility / Qualifications
Quality Assurance
- B.Pharm
- M.Pharm
- M.Sc
Experience: 2–7 Years
Quality Control
- B.Sc
- M.Sc Organic Chemistry
- M.Sc Analytical Chemistry
- B.Pharm
- M.Pharm
Experience: 3–7 Years
Microbiology
- B.Sc Microbiology
- M.Sc Microbiology
Experience: 3–7 Years
Relevant Education Background
B.Pharm, M.Pharm, B.Sc Chemistry, B.Sc Microbiology, M.Sc Microbiology, M.Sc Organic Chemistry, M.Sc Analytical Chemistry, M.Sc Pharmaceutical Chemistry, M.Sc Life Sciences.
Preferred Candidate Profile
Candidates should possess:
- Strong understanding of cGMP guidelines
- Knowledge of laboratory safety practices
- Experience in regulatory-approved pharmaceutical facilities
- Exposure to audit preparation and compliance activities
- Experience handling pharmaceutical quality systems
Location & Salary
Location: Matoda, Ahmedabad, Gujarat
Approximate Salary: ₹4.5 LPA – ₹10 LPA
Why Join Intas Pharmaceuticals?
Intas offers professionals the opportunity to work in a globally recognized pharmaceutical organization with strong exposure to regulated markets such as the US and EU.
Key Benefits
- Opportunity to Work in a Global Pharmaceutical Company
- Exposure to USFDA and EU Regulatory Standards
- Career Growth in Quality and Compliance Functions
- Experience in Regulated Manufacturing Facilities
- Participation in International Audit Programs
- Learning Opportunities Across Multiple Quality Functions
- Professional Development and Leadership Opportunities
For professionals aiming to build careers in pharmaceutical quality assurance, analytical quality control, microbiology, validation, and regulatory compliance, Intas provides a strong platform for long-term growth.
Application Process
Eligible candidates can directly attend the walk-in interview with all required documents.
Walk-In Interview Details
Date: 21st June 2026 (Sunday)
Time: 09:30 AM to 03:00 PM
Interview Venue
Intas Pharmaceuticals Ltd. – Matoda Facility
Plot No. 457 & 458
Sarkhej-Bavla Highway
Matoda Village, Sanand Taluka
Ahmedabad, Gujarat – 382210
Documents Required
Candidates should carry:
- Updated Resume
- Educational Certificates
- Experience Certificates
- Salary Documents
- Latest Payslips
- Government ID Proof
Important Instructions
- Candidates who have attended an interview at Intas within the last six months are requested not to apply.
- Applicants should have experience in regulatory-approved manufacturing facilities.
- Intas Pharmaceuticals does not charge any fee at any stage of recruitment.
Company Website
Frequently Asked Questions (FAQs)
1. Which departments are hiring in this walk-in drive?
Intas is hiring for Quality Assurance, Quality Control, and Microbiology departments.
2. What qualifications are accepted for Quality Assurance roles?
B.Pharm, M.Pharm, and M.Sc candidates with relevant experience can apply.
3. What experience is required for Quality Control positions?
Candidates should have 3–7 years of experience in pharmaceutical quality control functions.
4. Is experience in regulatory-approved facilities mandatory?
Yes. The company has specifically mentioned preference for candidates with experience in regulatory-approved pharmaceutical manufacturing facilities.
5. Can candidates who recently attended an Intas interview apply?
No. Candidates who appeared for an Intas interview within the last six months are requested not to apply.
6. Does Intas charge any recruitment fee?
No. Intas Pharmaceuticals clearly states that it does not charge any fee during the recruitment process.
Summary
| Category | Details |
|---|---|
| Company | Intas Pharmaceuticals Ltd. |
| Department Vacancies | Quality Assurance (QMS, Validation, IPQA), Quality Control, Microbiology |
| Qualification | B.Pharm, M.Pharm, B.Sc, M.Sc, M.Sc Microbiology, M.Sc Organic Chemistry, M.Sc Analytical Chemistry |
| Experience | 2–7 Years |
| Location | Matoda, Ahmedabad, Gujarat |

To apply for this job please visit www.intaspharma.com.