Aurobindo Pharma-Interviews for Production / Packing / QC / QA on 16th Mar’ 2024

Aurobindo Pharma-Interviews for Production / Packing / QC / QA on 16th Mar’ 2024

AUROBINDO PHARMA LTD (APL) is a leading Indian multinational pharmaceutical manufacturing firm with a turnover of over US$2.8 Billion in revenues for 2018-19. APL has a presence in more than 34 countries and exports products to 155 nations. Ranked as the 2nd Largest Generic Company in the USA by Rx dispensed, APL is also among the Top 10 Generic players in several European countries.

We are conducting Walk-In Interviews for multiple departments at APLHC-Unit IV.

1. Department: OSD Production

  • Roles: Compression, Capsule Filling & Coating
  • Qualification: ITI / Diploma / B.Sc.
  • Experience: 2 to 6 years

2. Department: OSD Packing

  • Roles: Bulk or Bottle Packing
  • Qualification: ITI / Diploma / B.Sc.
  • Experience: 2 to 6 years

3. Department: Quality Assurance

  • Roles: Cleaning Validation, QMS, Market Complaints, Training & Documentation
  • Qualification: B. Pharm / M. Pharma
  • Experience: 2 to 8 years

4. Department: Quality Control

  • Roles: IPFP, Stability, Microbiology, GLP
  • Qualification: M.Sc
  • Experience: 2 to 8 years

Documents to Carry:

  • Last 3 months pay slips
  • Last 6 months bank statement
  • Current CTC break-up sheet
  • All education documents
  • Aadhar & Pan Card
  • Date: March 16 2024
  • Venue: APL HEALTHCARE LIMITED, Unit-IV(SEZ),Plot No.16,APIIC, Multi Product SEZ, Menakuru, Naidupeta, Tirupati (Dt),AP.
Job Category: pharma
Job Type: Full Time
Job Location: Naidupeta Tirupati (Dt)

Apply for this position

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About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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