Ajanta Pharma Limited is conducting a walk-in interview for experienced Quality Assurance professionals at its Pithampur, Indore facility. Excellent opportunity for candidates with OSD (Oral Solid Dosage) manufacturing background seeking QA jobs, validation jobs, and QMS roles in a reputed pharmaceutical company with strong regulatory exposure (USFDA & MHRA).
About the Company
Ajanta Pharma Limited is a leading Indian multinational pharmaceutical company specializing in development, manufacturing, and marketing of high-quality branded generics across therapeutic segments including ophthalmology, dermatology, cardiology, and anti-infectives.
With state-of-the-art manufacturing facilities compliant with USFDA, MHRA, TGA, and other global regulators, Ajanta exports to over 30+ countries and maintains a strong presence in regulated markets.
The Pithampur (Indore) plant is a key OSD facility focused on quality excellence, innovation, and regulatory compliance. Ajanta is known for its employee-centric culture, continuous learning, and career progression opportunities in the pharma industry.
Job Details
- Company Name: Ajanta Pharma Limited
- Department: Quality Assurance (QA)
- Experience: 3–12 Years (varies by role)
- Qualification: B.Pharm / M.Pharm / B.Sc. / M.Sc.
- Location: Pithampur, Dist. Dhar, Indore, Madhya Pradesh
- Work Type: On-site
Job Description
Ajanta Pharma Limited invites dynamic professionals with OSD manufacturing experience for critical Quality Assurance roles involving online review, data integrity, qualification/validation, QMS documentation, and regulatory compliance. These positions support cGMP operations at the Pithampur OSD facility.
Officer/Sr. Officer – Lab QA
- Position: Officer / Sr. Officer (Lab QA)
- Experience: 3–8 Years
- Education/Qualification: B.Pharm / M.Pharm / B.Sc. / M.Sc.
Skills/Qualifications
- Experience in laboratory quality assurance for OSD products
- Proficiency in online review and pre-check of analytical data
- Knowledge of control sample management
- Strong investigation review skills
- Familiarity with cGMP, data integrity (ALCOA+), and regulatory requirements
Key Responsibilities
- Perform online review and pre-check of lab data
- Manage control sample storage and retrieval
- Review and close laboratory investigations
- Ensure compliance with pharmacopoeial and regulatory standards
- Support data integrity and audit readiness
Officer/Sr. Officer – QA (Qualification & Validation)
- Position: Officer / Sr. Officer (QA – Qualification & Validation)
- Experience: 3–12 Years
- Education/Qualification: B.Pharm / M.Pharm
Skills/Qualifications
- Hands-on exposure to Process Validation, Cleaning Validation, Hold Time Studies
- Experience in equipment and process qualification/requalification
- Proficiency in HVAC qualification and requalification
- Knowledge of QMS activities in OSD environment
- Regulatory exposure (USFDA, MHRA preferred)
Key Responsibilities
- Execute and review process, cleaning, and hold time validations
- Perform qualification/requalification of manufacturing equipment
- Conduct HVAC qualification and requalification activities
- Manage related QMS documentation and protocols
- Ensure compliance during validation lifecycle
Officer/Sr. Officer/Executive – QA (QMS)
- Position: Officer / Sr. Officer / Executive (QA – QMS)
- Experience: 4–12 Years
- Education/Qualification: B.Pharm / M.Pharm
Skills/Qualifications
- Experience in e-Log implementation and APQR preparation
- Proficiency in BMR/BPR/APQR review
- Knowledge of document scanning, movement, and control sample management
- Expertise in review and closure of Change Control, Deviation, CAPA, Incident
- Production QMS review and compliance
- Working exposure in USFDA/MHRA regulated environment
Key Responsibilities
- Implement and monitor electronic log systems
- Prepare and review Annual Product Quality Review (APQR)
- Review and close CC/Deviation/CAPA/Incident records
- Manage document control and movement
- Conduct production QMS reviews and ensure regulatory compliance
Benefits/Perks
- Opportunity to work in a USFDA/MHRA-approved OSD facility
- Career growth in a reputed multinational pharmaceutical company
- Exposure to global regulatory standards and quality systems
- Structured learning and professional development
- Stable work environment with focus on compliance and excellence
- Contribution to high-quality branded generics
How to Apply
Attend the walk-in interview with:
- Updated resume
- Current compensation letter
- One passport-size photograph
Important Notes:
- Candidates who appeared for interview in the last 6 months are not eligible.
- Ajanta Pharma does not charge any fees for recruitment—beware of fraudulent agencies or individuals.
For more QA jobs, validation jobs, and pharma opportunities in Madhya Pradesh and across India, explore listings on Pharma Recruiter.
Walk-in Interview Details
- Date: Wednesday, 25 February 2026
- Time: 10:00 AM to 04:00 PM
- Venue: Ajanta Pharma Limited Plot No. 55, 56, 57, ISEZ, Phase II Pithampur, Dist. Dhar – 454775, Madhya Pradesh
Why You Should Join
Ajanta Pharma Limited offers a platform to build a strong career in Quality Assurance within a globally compliant, OSD-focused manufacturing environment. With emphasis on regulatory excellence (USFDA, MHRA), data integrity, and QMS robustness, professionals gain valuable experience in high-standard operations.
Join a company recognized for quality, innovation, and employee growth—ideal for ambitious QA experts seeking long-term stability and impact in the pharmaceutical industry.
FAQs
Who is eligible for Ajanta Pharma QA walk-in?
Candidates with B.Pharm/M.Pharm/B.Sc./M.Sc. and 3–12 years of experience in OSD QA, preferably with USFDA/MHRA exposure.
What documents are required for the interview?
Updated resume, current compensation letter, and one passport-size photograph.
Can freshers or non-OSD candidates apply?
No—only candidates with relevant OSD experience are considered; those interviewed in last 6 months are ineligible.
Is there any recruitment fee charged by Ajanta Pharma?
No—Ajanta does not seek any payment for employment. Report any such requests immediately.