Explore top QA jobs at Ajanta Pharma’s US FDA-approved facility in Maharashtra. Ideal for pharmaceutical careers in India with 3-4 years exp. Apply by Oct 27, 2025!
Contents
About the Company
Ajanta Pharma Limited, a leading specialty pharmaceutical company headquartered in Mumbai, India, excels in developing, manufacturing, and marketing branded generic medicines across 30+ countries.
With a strong global footprint in India, the US, Europe, and emerging markets, Ajanta drives innovation in ophthalmology, dermatology, and cardiology therapies.
Certified as a Great Place to Work, it upholds rigorous US FDA and EMA compliance, fostering sustainable growth and empowering over 3,000 employees through cutting-edge facilities and a commitment to quality in pharmaceutical careers in India.
Job Details
- Company Name: Ajanta Pharma Limited
- Experience: 3-4 Years
- Qualification: B.Pharm / M.Sc.
- Location: B-4/5/6, MIDC Area, Paithan, Dist: Chhatrapati Sambhajinagar, Maharashtra – 431148
- Work Type: On-site
Job Description
Ajanta Pharma Limited is seeking dedicated professionals for its US FDA-approved oral solid dosage (OSD) formulation facility in Paithan. This QA role focuses on training coordination to ensure seamless operations and compliance. Perfect for those advancing in pharma jobs and QA jobs within a globally recognized innovator.
Officer – Quality Assurance
- Department: Quality Assurance
- Role: Coordinate training programs and maintain records in OSD FDA facility
- Experience: 3-4 Years
- Education/Qualification: B.Pharm / M.Sc.
Skills/Qualifications
- Exposure to OSD formulation in US FDA-approved facilities
- Proficiency in maintaining training records, matrices, and attendance sheets
- Strong coordination skills for GMP and job-specific training sessions
- Experience in cross-departmental collaboration for training execution
- Knowledge of induction training processes for new joiners
- Familiarity with training applications like TRIMS
Key Responsibilities
- Update training records and attendance matrices
- Coordinate GMP and job-specific sessions
- Facilitate cross-departmental training planning
- Manage induction for new employees
- Ensure TRIMS application compliance
- Support OSD facility quality standards
Benefits/Perks
- Career advancement in a Great Place to Work-certified firm
- Professional development through specialized training
- Competitive salary and performance incentives
- Supportive work culture emphasizing collaboration
- Global exposure to international pharma standards
How to Apply
Interested candidates should email their resume to cv.ptn@ajantapharma.com with “Officer – Quality Assurance – Paithan” in the subject line. Applications are valid until October 27, 2025.
For more QA jobs and pharmaceutical careers in India, visit Pharma Recruiter. Apply now to join a leader in specialty pharma!
Why You Should Join
Ajanta Pharma Limited nurtures a culture of excellence and employee recognition, where QA professionals drive compliance in innovative OSD manufacturing. Gain long-term career stability in a multinational powerhouse with robust growth trajectories in global markets.
Thrive amid continuous learning opportunities, expert mentorship, and a compliance-focused environment that rewards contributions to quality medicines, elevating your pharma jobs journey.
FAQs
Who is eligible for the QA Officer role at Ajanta Pharma?
Candidates with B.Pharm/M.Sc. and 3-4 years in OSD formulation, especially FDA-approved facilities, are ideal for these QA jobs.
What is the application process?
Email your resume to cv.ptn@ajantapharma.com by October 27, 2025. Include relevant experience highlights for faster review.
What does the role entail in terms of training?
Focus on GMP coordination, record maintenance, and TRIMS usage to support smooth operations in the Paithan facility.
What growth opportunities exist post-hiring?
Expect promotions in QA leadership, global projects, and skill-building for pharmaceutical careers in India.
i need job nd i am fresher