Ajanta Pharma Hiring Quality Control Officer
- Company Overview
- Job Role & Responsibilities
- Officer – Quality Control (GLP Section)
- Eligibility / Qualifications
- Educational Qualification
- Experience Requirements
- Key Skills & Competencies
- Location & Salary
- Application Process
- FAQs
- Who can apply for this Quality Control Officer role?
- Is experience in US FDA–approved facilities mandatory?
- What type of QC work does this role involve?
- Where is the job location?
- How do I apply?
- Summary Table
B.Sc/M.Sc QC Officer Jobs | Ajanta Pharma Paithan
Ajanta Pharma hiring Quality Control Officer with 3–5 years experience at Paithan, Maharashtra. B.Sc/M.Sc eligible. Apply now.
Ajanta Pharma Limited is inviting applications from experienced quality professionals to strengthen its Quality Control – GLP division at its US FDA–approved formulation manufacturing facility located in Paithan, Chhatrapati Sambhajinagar, Maharashtra. This opportunity is ideal for pharmaceutical professionals seeking stable, long-term careers in regulated manufacturing environments with strong exposure to global compliance standards.
The opening is particularly relevant for candidates actively searching for quality control officer jobs in pharma, GLP laboratory roles, USFDA QC jobs in Maharashtra, and mid-level quality control positions in formulation plants. Ajanta Pharma offers a structured work culture, robust quality systems, and growth opportunities within a globally trusted pharmaceutical organization.
Company Overview
Ajanta Pharma Limited is a well-established pharmaceutical company with a strong global presence across branded generics, specialty products, and regulated markets. The organization operates multiple world-class manufacturing facilities approved by US FDA, EU GMP, WHO, and other international regulatory authorities.
The Paithan manufacturing site in Maharashtra is a key formulation facility known for its strict adherence to Good Laboratory Practices (GLP), data integrity standards, and advanced analytical infrastructure. Being Great Place to Work–Certified in 2025 reflects Ajanta Pharma’s focus on employee well-being, ethical practices, and long-term career development.
Job Role & Responsibilities
Officer – Quality Control (GLP Section)
The selected candidate will be responsible for ensuring laboratory compliance, equipment readiness, and data integrity within the Quality Control GLP section.
Key responsibilities include:
- Managing calibration, qualification, and preventive maintenance activities for laboratory instruments
- Handling computerized systems, electronic data, and user access controls in compliance with data integrity norms
- Supporting smooth operation of analytical instruments and initiating corrective actions during breakdowns
- Executing laboratory instrument validation and qualification protocols
- Preparing, executing, and evaluating supplementary analytical studies under variable conditions
- Ensuring ALCOA principles are followed for accurate and compliant data recording
- Managing working standards, reference standards, chemicals, reagents, and laboratory glassware
- Supporting audits and regulatory inspections related to GLP and QC systems
This role plays a critical part in maintaining analytical accuracy, regulatory compliance, and product quality for patient safety.
Eligibility / Qualifications
Educational Qualification
B.Sc, M.Sc (Chemistry or relevant science discipline)
Experience Requirements
- 3 to 5 years of relevant experience in pharmaceutical Quality Control laboratories
- Prior exposure to GLP environments in formulation manufacturing plants
- Experience in US FDA or EU GMP–approved facilities is highly preferred
Key Skills & Competencies
- Strong understanding of laboratory compliance and data integrity
- Hands-on knowledge of analytical laboratory operations
- Familiarity with regulatory documentation and audit readiness
- Detail-oriented mindset with strong compliance discipline
Location & Salary
The position is based at Ajanta Pharma Limited’s formulation facility in Paithan, Chhatrapati Sambhajinagar district, Maharashtra. Salary will be offered as per industry standards and commensurate with experience, skills, and current compensation.
Application Process
Interested and eligible candidates may share their updated resume at:
Candidates are advised to apply before 06 January 2026, as this hiring communication is valid only until that date.
FAQs
Who can apply for this Quality Control Officer role?
Candidates with a B.Sc or M.Sc degree and 3–5 years of experience in pharmaceutical QC laboratories can apply.
Is experience in US FDA–approved facilities mandatory?
It is preferred but not mandatory. Candidates with strong GLP and QC exposure will be considered.
What type of QC work does this role involve?
The role focuses on GLP compliance, laboratory equipment management, validation activities, and data integrity.
Where is the job location?
The role is based at Ajanta Pharma Limited, MIDC Area, Paithan, Maharashtra.
How do I apply?
Email your updated CV to cv.ptn@ajantapharma.com before the application deadline.
Summary Table
| Company | Ajanta Pharma Limited |
|---|---|
| Vacancies | Officer – Quality Control (GLP Section) |
| Required Education | B.Sc, M.Sc (Chemistry or relevant discipline) |
| Experience | 3–5 years |
To apply for this job email your details to cv.ptn@ajantapharma.com
