Are you a skilled Quality Control professional with experience in pharmaceutical GLP environments? Ajanta Pharma Limited is hiring for the position of Quality Control Officer in its GLP section at the US FDA-approved formulation facility in Paithan, Maharashtra. This role offers an excellent opportunity for candidates with 3–5 years of experience to contribute to global compliance standards and ensure product quality in a reputed organization.

With a focus on data integrity, instrument management, and regulatory audits, this position is perfect for those searching for QC Officer jobs in pharma, GLP QC roles in Maharashtra, or mid-level positions in USFDA-approved plants.

Company Overview

Ajanta Pharma Limited is a leading specialty pharmaceutical company with a robust global footprint in branded generics and regulated markets. The company operates multiple state-of-the-art manufacturing facilities approved by US FDA, EU GMP, WHO, and other stringent authorities.

The Paithan site in Chhatrapati Sambhajinagar district stands out for its advanced analytical capabilities, strict adherence to Good Laboratory Practices (GLP), and commitment to employee growth. Certified as a Great Place to Work in 2025, Ajanta Pharma prioritizes ethical practices, work-life balance, and professional development.

Job Role & Responsibilities

Position: Officer – Quality Control (GLP Section)

The role involves maintaining laboratory compliance and supporting high-quality analytical operations in a regulated environment. Key responsibilities include:

• Managing calibration, qualification, and preventive maintenance of laboratory instruments
• Handling computerized systems, electronic data management, and user access controls per data integrity guidelines
• Troubleshooting analytical instrument breakdowns and ensuring operational readiness
• Executing validation and qualification protocols for laboratory equipment
• Conducting supplementary analytical studies under varying conditions
• Ensuring adherence to ALCOA principles for accurate data documentation
• Managing reference standards, working standards, chemicals, reagents, and glassware inventory
• Supporting internal audits and regulatory inspections for GLP and QC compliance

This position is vital for upholding analytical excellence and patient safety through rigorous quality standards.

Required Qualifications & Eligibility

Educational Qualification

• B.Sc or M.Sc in Chemistry or relevant science discipline

Experience Requirements

• 3 to 5 years in pharmaceutical Quality Control laboratories
• Hands-on experience in GLP sections of formulation manufacturing units
• Exposure to US FDA or EU GMP-approved facilities (highly preferred)

Key Skills & Competencies

• In-depth knowledge of laboratory compliance and data integrity practices
• Proficiency in analytical instrument operations and troubleshooting
• Familiarity with regulatory documentation and audit preparation
• Strong attention to detail and commitment to compliance

Location, Salary & Benefits

The job is located at Ajanta Pharma’s formulation manufacturing facility in MIDC Area, Paithan, Chhatrapati Sambhajinagar, Maharashtra.

Salary will be competitive and aligned with industry standards, typically ranging from INR 4–6 Lakhs per annum based on experience, skills, and qualifications. Ajanta Pharma offers attractive benefits including professional growth opportunities, structured training, and a supportive work culture in a Great Place to Work-certified environment.

How to Apply

Eligible candidates should email their updated resume to cv.ptn@ajantapharma.com.

Applications are invited until 06 January 2026. Early submissions are encouraged as the hiring process may close sooner based on suitable candidate availability.

Frequently Asked Questions (FAQs)

Who is eligible for this QC Officer role? Candidates holding B.Sc/M.Sc with 3–5 years of relevant pharma QC experience, preferably in GLP environments.

Is US FDA facility experience required? It is highly preferred, but candidates with strong GLP and QC backgrounds will also be considered.

What does the role primarily focus on? GLP compliance, equipment management, validation, and data integrity in the Quality Control laboratory.

Where is the job based? Paithan, Chhatrapati Sambhajinagar district, Maharashtra (on-site role).

How can I apply? Send your CV to cv.ptn@ajantapharma.com before the deadline.