Aurobindo Pharma Limited has announced a Walk-in Recruitment Drive for its Unit III, Bachupally, Hyderabad facility. The company is inviting applications from freshers (2022–2026 pass-outs) and experienced professionals (2–6 years) for multiple positions in Production, Packing, Quality Control, and Quality Assurance departments.

This is an excellent opportunity for candidates looking to build a career in the pharmaceutical manufacturing industry, especially in Oral Solid Dosage (OSD) operations.

Aurobindo Pharma Recruitment Overview

Particular Details

Company Name

Aurobindo Pharma Ltd.

Job Type

Walk-in Interview

Department

Production, Packing, Quality Control, Quality Assurance

Job Location

Bachupally, Hyderabad

Experience

Freshers & 2–6 Years

Qualification

ITI, Diploma, B.Sc, B.Pharm, M.Pharm, M.Sc

Interview Date

02 August 2026 (Sunday)

Interview Time

10:00 AM to 01:00 PM

Shift

Rotational Shifts

Department-wise Vacancy Details

1. Production

Position: TA

Area of Work:

Compression

Coating

Granulation

Qualification:

ITI

Diploma

B.Sc

2. Packing

Position: TA / Executive

Area of Work:

Bottle Packing

Blister Packing

Liquid Filling

Dry Syrup

Primary Packing

Secondary Packing

Qualification:

B.Pharm

M.Pharm

ITI

Diploma

B.Sc

3. Quality Control (QC)

Position: Executive

Area of Work:

Stability Testing

Gas Chromatography (GC)

Qualification:

M.Sc

B.Pharm

M.Pharm

4. Quality Assurance (QA)

Position: Executive

Area of Work:

IPQA (In-Process Quality Assurance)

Qualification:

B.Pharm

M.Pharm

Experience Required

2–6 years of experience in OSD Manufacturing

Candidates should be willing to work in rotational shifts.

Freshers Eligibility

Fresh candidates from the following pass-out years are encouraged to attend:

2022

2023

2024

2025

2026

Eligible qualifications:

B.Pharm

B.Sc (Chemistry)

Diploma

ITI

Freshers are eligible for Production and Packing departments.

Walk-in Interview Details

Date: 02 August 2026 (Sunday)

Time: 10:00 AM to 01:00 PM

Venue: Aurobindo Pharma Ltd. – Unit III

Bachupally, Hyderabad – 500090

Documents Required

Candidates should carry:

Updated Resume

Educational Certificates

PAN Card

Aadhaar Card

Recent Increment Letter (if applicable)

Current CTC Details

Last 3 Months Payslips

Bank Statement

Passport-size Photographs

Why Join Aurobindo Pharma?

One of India’s leading pharmaceutical manufacturers.

Excellent learning opportunities in OSD manufacturing.

Exposure to GMP-compliant production facilities.

Career growth through structured training and development.

Competitive salary and employee benefits.

Selection Process

Registration

Document Verification

Technical Interview

HR Interview

Final Selection

Important Note

Aurobindo Pharma follows a strict merit-based recruitment process. The company does not charge any recruitment fee or security deposit. Candidates should beware of fraudulent job offers.

Technical FAQs

1. What is OSD manufacturing in the pharmaceutical industry?

OSD (Oral Solid Dosage) manufacturing involves the production of tablets, capsules, and other solid oral medicines through processes such as granulation, compression, coating, and packaging while complying with GMP guidelines.

2. What is IPQA in Quality Assurance?

IPQA (In-Process Quality Assurance) monitors manufacturing activities during production to ensure products meet predefined quality standards, SOPs, and regulatory requirements.

3. What is Stability Testing in Quality Control?

Stability testing evaluates how a pharmaceutical product maintains its quality, potency, safety, and shelf life under different environmental conditions such as temperature and humidity.

4. What is the role of Gas Chromatography (GC) in pharmaceutical QC?

Gas Chromatography is an analytical technique used to identify and quantify volatile compounds, residual solvents, and impurities to ensure compliance with pharmacopeial specifications.

5. What GMP practices should candidates know before attending a pharmaceutical interview?

Candidates should understand Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), SOP compliance, data integrity (ALCOA+ principles), personal hygiene, contamination control, line clearance, and safety procedures.