Intas Walk-In QA QC Micro Engineering

Intas Hiring QA QC Micro Engineering | Ahmedabad

Intas Pharmaceuticals hiring QA, QC Micro, Stability & Engineering professionals. B.Pharm, MSc, BE, BTech with 3-10 years experience. Ahmedabad.

Professionals seeking career opportunities in Quality Assurance, Quality Control, Microbiology, Engineering, and regulated pharmaceutical manufacturing can explore the latest walk-in drive announced by Intas Pharmaceuticals Ltd. The company is conducting a recruitment drive for experienced professionals at its SEZ manufacturing facility in Ahmedabad.

Intas Pharmaceuticals is hiring for Quality Control Microbiology (Environment Monitoring), Quality Assurance Qualification, Stability Sample Management, Quality Control, and Engineering departments. Candidates with experience in USFDA, MHRA, and EU-regulated pharmaceutical plants are encouraged to attend the walk-in interview.

For job seekers searching for pharmaceutical quality assurance jobs, QC microbiology careers, engineering maintenance jobs, regulatory compliance positions, GMP pharmaceutical vacancies, and formulation manufacturing opportunities, this hiring drive offers an excellent chance to join one of India’s leading multinational pharmaceutical companies.

Company Overview

About Intas Pharmaceuticals

Intas Pharmaceuticals Limited is one of the world’s leading pharmaceutical formulation development, manufacturing, and marketing organizations. The company has established a strong global presence across more than 85 countries and continues to expand its footprint in highly regulated international markets.

A significant portion of Intas’ revenue comes from regulated regions including the United States and Europe. The company operates advanced manufacturing facilities that comply with stringent international quality standards and regulatory requirements.

With a strong focus on innovation, patient care, quality systems, and operational excellence, Intas offers professionals opportunities to build rewarding careers within globally recognized pharmaceutical operations.

Job Role & Responsibilities

Department: Quality Control – Microbiology (Environment Monitoring)

Position

• Executive
• Senior Officer

Qualification

• M.Sc
• B.Pharm

Experience

• 4 to 9 Years

Key Responsibilities

• Environmental monitoring activities.
• Microbiological testing and analysis.
• Cleanroom monitoring and compliance.
• Trend analysis and reporting.
• Investigation of microbiological deviations.
• Regulatory documentation and record maintenance.
• Compliance with GMP and data integrity requirements.

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Department: Quality Assurance – Qualification (OSD/Injectable)

Position

• Officer
• Senior Officer

Qualification

• M.Sc
• B.Pharm

Experience

• 3 to 7 Years

Key Responsibilities

• Equipment qualification activities.
• Facility qualification and validation support.
• Protocol preparation and execution.
• Documentation review and approval.
• GMP compliance monitoring.
• Regulatory inspection readiness activities.

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Department: Quality Assurance – Stability Sample Management

Position

• Officer
• Senior Officer

Qualification

• M.Sc
• B.Pharm

Experience

• 3 to 7 Years

Key Responsibilities

• Stability sample management.
• Stability protocol execution.
• Sample tracking and storage activities.
• Documentation and compliance management.
• Coordination with quality control laboratories.
• Regulatory stability program support.

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Department: Quality Control

Position

• Executive
• Senior Officer
• Officer

Qualification

• M.Sc
• B.Pharm

Experience

• 4 to 9 Years

Key Responsibilities

• Raw material testing.
• Finished product analysis.
• Stability sample testing.
• Laboratory investigations.
• Instrument operation and calibration.
• Data review and documentation.
• Compliance with GLP and GMP requirements.

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Department: Engineering – Plant Maintenance / Instrumentation

Position

• Executive
• Senior Executive

Qualification

• B.E.
• B.Tech

Experience

• 4 to 10 Years

Key Responsibilities

• Preventive and breakdown maintenance.
• Instrumentation system management.
• Utility equipment monitoring.
• Calibration support activities.
• Plant maintenance planning.
• Engineering compliance and documentation.

Eligibility / Qualifications

Educational Qualification

Candidates should possess any of the following qualifications:

• B.Pharm
• M.Sc
• B.E.
• B.Tech

Relevant Courses

B.Pharm, Pharmaceutical Analysis, Pharmaceutical Technology, Quality Assurance, Industrial Pharmacy, M.Sc Chemistry, M.Sc Microbiology, M.Sc Biotechnology, Analytical Chemistry, Pharmaceutical Chemistry, Instrumentation Engineering, Mechanical Engineering, Electrical Engineering, Industrial Engineering, Process Engineering, Validation and Qualification Studies.

Experience Required

• Quality Assurance: 3 to 7 Years
• Quality Control Microbiology: 4 to 9 Years
• Quality Control: 4 to 9 Years
• Engineering: 4 to 10 Years

Mandatory Requirements

Candidates should have:

• Experience in formulation pharmaceutical manufacturing.
• Exposure to regulated manufacturing facilities.
• Knowledge of USFDA, MHRA, and EU regulatory environments.
• Willingness to work in rotational shifts where applicable.
• Strong GMP and compliance knowledge.

Preferred Industry Background

Applicants from regulated pharmaceutical facilities involved in Oral Solid Dosage (OSD), Injectable Manufacturing, Quality Assurance, Quality Control, Validation, Stability Studies, Engineering Maintenance, and Microbiology functions will be preferred.

Why Join Intas Pharmaceuticals?

Intas Pharmaceuticals is recognized as one of the fastest-growing multinational pharmaceutical companies with a strong presence in regulated global markets. Working at Intas provides professionals with exposure to international quality standards, advanced manufacturing technologies, and global regulatory systems.

Career Benefits

• Work with a leading multinational pharmaceutical company.
• Exposure to USFDA, MHRA, and EU-regulated operations.
• Opportunities for career growth and professional development.
• Experience with advanced pharmaceutical quality systems.
• Competitive compensation and employee benefits.
• Learning opportunities in global healthcare manufacturing.
• Long-term career prospects within regulated pharmaceutical environments.

Professionals interested in pharmaceutical quality assurance careers, microbiology jobs, engineering maintenance positions, regulatory affairs opportunities, validation jobs, and quality control careers can significantly benefit from joining Intas Pharmaceuticals.

Walk-In Interview Details

Interview Date

06 June 2026 (Saturday)

Interview Time

09:30 AM to 04:00 PM

Interview Venue

Intas Pharmaceuticals Ltd. (Pharmez)
Plot No. 5 to 14, Pharmez
Near Village Matoda
Sarkhej-Bavla National Highway No. 8-A
Taluka Sanand
Ahmedabad – 382213
Gujarat

Job Location

Intas Pharmez, Ahmedabad

Documents Required

Candidates should carry:

• Updated Resume
• Educational Certificates
• Final Year Mark Sheets
• Degree Certificates
• Experience Certificates
• Current CTC Breakup
• Latest Salary Slips
• Original Documents
• Photocopies of Supporting Documents

Important Instructions

• Candidates who attended an Intas interview within the last six months are requested not to apply.
• Relevant pharmaceutical formulation experience is mandatory.
• Exposure to regulated plants such as USFDA, MHRA, and EU-approved facilities is preferred.
• Candidates should be willing to work in shifts where required.

Location & Salary

Location: Ahmedabad

Estimated Salary: ₹5.5 LPA – ₹15 LPA (Approximate salary based on experience, designation, department, and current pharmaceutical industry standards)

Application Process

Interested candidates can directly attend the walk-in interview on the scheduled date.

For company information and career opportunities:

Website: www.intaspharma.com

Recruitment Notice

Intas Pharmaceuticals does not charge any fee for applications, recruitment processing, interviews, training, or employment. Candidates should avoid fraudulent recruitment offers and refrain from making any payments to individuals claiming to represent the company.

Frequently Asked Questions (FAQs)

1. Which departments are hiring in this Intas walk-in drive?

The company is hiring for Quality Assurance, Quality Control, Microbiology (Environment Monitoring), Stability Sample Management, and Engineering departments.

2. What qualifications are required?

Candidates with B.Pharm, M.Sc, B.E., and B.Tech qualifications can apply depending on the position.

3. Is regulated plant experience mandatory?

Yes. Experience in regulated pharmaceutical facilities such as USFDA, MHRA, or EU-approved plants is preferred.

4. What is the experience requirement?

The company is hiring candidates with 3 to 10 years of relevant pharmaceutical experience.

5. Are shift duties applicable?

Yes. Several quality-related positions require candidates to work in shifts.

6. How can candidates apply?

Candidates can directly attend the walk-in interview at the specified venue on 06 June 2026.

Summary

Intas Pharmaceuticals is conducting a walk-in drive for Quality Assurance, Quality Control, Microbiology, Stability Management, and Engineering professionals at its Ahmedabad SEZ facility. Candidates with B.Pharm, M.Sc, B.E., and B.Tech qualifications and experience in regulated pharmaceutical plants are encouraged to attend.

Company	Intas Pharmaceuticals Ltd.
Department Vacancies	QA Officer/Sr. Officer, QC Executive/Sr. Officer, QC Micro Executive/Sr. Officer, Engineering Executive/Sr. Executive
Qualification	B.Pharm, M.Sc, B.E., B.Tech
Experience	3–10 Years
Location	Ahmedabad