Ajanta Pharma Hiring Quality Control Officer
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Eligibility / Qualifications
- Educational Requirements
- Experience Requirements
- Required Skills
- Location & Salary
- Application Process
- Frequently Asked Questions
- Who can apply for this Quality Control Officer role?
- Is experience with US FDA plants mandatory?
- What instruments will I work on?
- Where is the job located?
- How do I apply?
- Summary Table
Ajanta Pharma hiring Quality Control Officer in Paithan. B.Sc/M.Sc with 3–5 years QC experience in USFDA plant eligible.
Ajanta Pharma Limited is hiring experienced Quality Control professionals for its US FDA approved formulation manufacturing facility located at Paithan, District Chhatrapati Sambhajinagar, Maharashtra. This opportunity is ideal for analytical quality professionals who want to work in a regulated, audit-driven environment and contribute directly to the release of high-quality oral solid dosage products for domestic and international markets. The role offers strong exposure to FDA-compliant systems, advanced laboratory instrumentation, and robust quality processes.
Company Overview
Ajanta Pharma Limited is a globally recognized pharmaceutical company with a strong presence in branded generics across regulated and semi-regulated markets. The company operates multiple US FDA approved manufacturing facilities and is known for its consistent compliance record, science-led approach, and focus on quality-driven growth.
Ajanta Pharma’s formulation facility at Paithan plays a key role in supplying high-quality medicines to global markets. The site operates under stringent regulatory oversight and follows international quality standards including US FDA, WHO-GMP, and other global regulatory guidelines. Professionals working at Ajanta Pharma gain hands-on exposure to audit-facing operations, advanced quality systems, and continuous improvement initiatives.
Job Role & Responsibilities
The Quality Control Officer will be responsible for analytical testing, laboratory compliance, and quality monitoring activities within the formulation QC and microbiology laboratories.
Key Responsibilities
- Perform analysis of finished products, in-process samples, raw materials, and stability samples
- Support process validation and stability study activities
- Operate and maintain analytical instruments including HPLC, GC, UV Spectrophotometer, Dissolution Apparatus, and IR
- Execute laboratory activities in compliance with approved SOPs and test methods
- Utilize LIMS (Caliber) for sample management, data entry, and result reporting
- Monitor and ensure adherence to Good Laboratory Practices (GLP) in QC and Microbiology labs
- Review analytical data for accuracy, completeness, and compliance
- Support investigations related to OOS, OOT, and laboratory deviations
- Maintain proper documentation and data integrity as per regulatory expectations
- Assist during internal audits, regulatory inspections, and compliance reviews
This role is critical in ensuring that only compliant, safe, and effective pharmaceutical products are released to the market.
Eligibility / Qualifications
Educational Requirements
- B.Sc or M.Sc in relevant science disciplines
Relevant Courses (comma-separated): B.Sc Chemistry, M.Sc Chemistry, M.Sc Pharmaceutical Sciences, Analytical Chemistry, Industrial Chemistry
Experience Requirements
- 3 to 5 years of experience in pharmaceutical Quality Control
- Mandatory exposure to OSD formulation manufacturing in a US FDA approved facility
- Hands-on experience with analytical instruments used in QC laboratories
Required Skills
- Strong understanding of pharmaceutical QC testing and documentation
- Practical knowledge of test methods and instrumental techniques
- Experience working with LIMS systems, preferably Caliber
- Familiarity with GLP, GMP, and data integrity requirements
- Ability to work in audit-facing, regulated environments
Location & Salary
- Work Location: Ajanta Pharma Ltd, B-4/5/6 MIDC Area, Paithan, District Chhatrapati Sambhajinagar, Maharashtra – 431148
- Employment Type: Full-time
- Salary: Competitive and aligned with industry standards based on experience
Application Process
Interested and eligible candidates can apply by sharing their updated resume at the email address below:
This hiring communication is valid until January 25, 2026. Candidates are advised to apply at the earliest.
Frequently Asked Questions
Who can apply for this Quality Control Officer role?
Candidates with B.Sc or M.Sc qualifications and 3–5 years of QC experience in a US FDA approved OSD facility can apply.
Is experience with US FDA plants mandatory?
Yes. Prior exposure to US FDA approved formulation facilities is required.
What instruments will I work on?
You will handle HPLC, GC, UV, Dissolution, IR, and related QC laboratory instruments.
Where is the job located?
The position is based at Ajanta Pharma’s Paithan facility in Maharashtra.
How do I apply?
Send your resume to cv.ptn@ajantapharma.com before the application deadline.
Summary Table
| Company | Ajanta Pharma Limited |
|---|---|
| Vacancies | Quality Control Officer |
| Required Education | B.Sc, M.Sc |
| Experience | 3–5 Years |
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