Ajanta Pharma Hiring Quality Control Officer

Ajanta Pharma Limited; Maharashtra; Presencial; INR 450.000 - 650.000; Jornada completa

Descripción de la vacante

Ajanta Pharma Limited in Paithan, Maharashtra, invites applications for a Quality Control Officer with a B.Sc or M.Sc and 3–5 years of QC experience in a US FDA approved facility. The role focuses on analytical testing, compliance, and data integrity in formulation QC and microbiology labs.

You will work with HPLC, GC, UV, dissolution and IR systems, ensure GLP compliance, support investigations into OOS/OOT, and assist during audits. Competitive salary based on experience.

Formación

• B.Sc or M.Sc in relevant science disciplines.
• 3–5 years of experience in pharmaceutical QC in US FDA approved facility.
• Hands-on experience with analytical instruments used in QC laboratories.

Responsabilidades

• 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.
• Ensure GLP compliance and data integrity; document thoroughly.

Conocimientos

QC testing

GLP compliance

Documentation

Audit readiness

LIMS experience

Educación

B.Sc or M.Sc in relevant science

Herramientas

HPLC

GC

UV-Vis

Dissolution

IR

Caliber LIMS

Descripción del empleo

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

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.

Summary Table

• Company: Ajanta Pharma Limited
• Vacancies: Quality Control Officer
• Required Education: B.Sc, M.Sc
• Experience: 3–5 Years