Aurobindo Pharma Walk-In Interview for Production, Packing, QA, QC Roles

Aurobindo Pharma recruitment notification
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  • Full Time
  • Anywhere

Website Aurobindo pharma Limited

Committed to healthier life

Aurobindo Pharma, the second-largest listed Indian pharmaceutical company by revenue, is renowned for its global presence in over 155 countries. With 29 state-of-the-art manufacturing facilities and a workforce of over 23,000 professionals, Aurobindo is a leader in delivering quality healthcare products.

If you’re looking to build a career in a dynamic and rewarding environment, this is your chance to join a globally recognized brand at its Jadcherla unit.


Walk-In Interview Details

  • Date: 07 December 2024 (Saturday)
  • Time: 09:30 AM to 03:00 PM
  • Venue: APL Health Care Limited, Unit-1, Jadcherla, SEZ, Polepally, Mahabubnagar, Telangana – 509302

Available Roles and Requirements

1. Production (Manufacturing)

  • Key Skills: Compression, Coating, Capsule Filling, Encapsulation
  • Qualifications: ITI/Diploma/BSc/B Pharm
  • Positions: Technical Assistant, Senior Technical Assistant, Executive
  • Experience: 3-6 years

2. Packing

  • Key Skills: Bottle/Powder Filling, Sachet, Tablet Counting Line, Bottle Filling Line (Bottle/Jar/Sachet)
  • Qualifications: ITI/Diploma/BSc/B Pharm
  • Positions: Technical Assistant, Senior Technical Assistant, Executive
  • Experience: 3-6 years

3. Quality Control (QC)

  • Key Skills: Hands-on experience with HPLC, BU, CU, Dissolution Profiles, and QC Instrument Qualification
  • Qualifications: B Pharm/MSc
  • Positions: Executive
  • Experience: Regulatory exposure (e.g., USFDA, MHRA) preferred

4. Quality Assurance (QA)

  • Key Skills: IPQA, Validations, Equipment Qualification
  • Qualifications: B Pharm
  • Positions: Executive
  • Experience: 3-6 years

How to Prepare for the Interview?

  1. Bring an updated resume, passport-sized photographs, and educational certificates.
  2. Ensure all documents highlight your qualifications and experience relevant to the role.
  3. Be ready to discuss your technical expertise and exposure to regulatory standards.


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