Join Lupin Limited Vacancies in Quality Assurance and Control

Lupin Limited Recruitment Notification

Vacancy in Quality at Lupin Limited

Embark on a rewarding career journey with Lupin Limited, a prominent innovation-led transnational pharmaceutical company. This is your golden opportunity to become part of a dynamic and results-driven team at our USFDA-approved formulation facility in Aurangabad.

About the Company

Lupin Limited is a leading pharmaceutical manufacturer in India, known for its commitment to innovation and excellence. With a state-of-the-art facility in Aurangabad, Lupin is dedicated to producing high-quality pharmaceuticals. We are currently seeking young, dynamic professionals to join us in our expansion journey.

Company Vacancies List

Explore exciting job opportunities in the Quality Department:

Officer – Quality Assurance

  • Qualification: B. Pharma
  • Experience: 3-7 Years
  • Responsibilities:
    • Line clearance and in-process checks.
    • Compliance monitoring at the shop floor.
    • GMP document issuance and retrieval.
    • Protocol and report review.
    • Exposure to formulation OSD (Tablet/capsules) in USFDA/UK/MHRA approved company.

Officer – Quality Assurance

  • Qualification: B. Pharma
  • Experience: 3-7 Years
  • Responsibilities:
    • QMS & Documentation.
    • Handling market complaints.
    • GMP document issuance and retrieval.
    • SMR and BPR review.
    • Quality risk assessment, change control, CAPA, internal audit.
    • Exposure to formulation OSD (Tablet/capsules) in USFDA/UK/MHRA approved company.

Officer – Quality Control

  • Qualification: BSc/MSc/B Pharm
  • Experience: 3-5 Years
  • Responsibilities:
    • Analysis of finished products, raw materials, stability samples.
    • Instrument operation and calibration knowledge.
    • Familiar with regulatory inspections (USFDA, WHO, etc.).
    • Exposure to formulation OSD (Tablet/capsules) in USFDA/UK/MHRA approved company.

Executive – Quality Control (Micro)

  • Qualification: B.Sc./MSc/B Pharm
  • Experience: 4-8 Years
  • Responsibilities:
    • Microbial limit test validation, MIT testing.
    • Environment monitoring, water sampling and analysis.
    • Culture/biobell handling, autoclave validation.
    • Exposure to formulation OSD (Tablet/capsule) in USFDA/UK/MHRA approved company.

Executive – Quality Control

  • Qualification: B.Sc./MSc/B Pharm
  • Experience: 3-7 Years (If < 5 years, minimum 60%)
  • Responsibilities:
    • EMDS/LIMS specification review.
    • STP/SPEC/TOS support.
    • UMS-related CVV documentation.
    • Computer system and software validations.
    • Exposure to formulation OSD (Tablet/capsule) in USFDA/UK/MHRA approved company.

Important Note: Candidature is not applicable if interviewed in the last 6 months for any Lupin location.

Job Description

Officer – Quality Assurance

  • Line clearance and in-process checks.
  • Compliance monitoring at the shop floor.
  • GMP document issuance and retrieval.
  • Protocol and report review.
  • Exposure to formulation OSD (Tablet/capsules) in USFDA/UK/MHRA approved company.

Officer – Quality Assurance

  • QMS & Documentation.
  • Handling market complaints.
  • GMP document issuance and retrieval.
  • SMR and BPR review.
  • Quality risk assessment, change control, CAPA, internal audit.
  • Exposure to formulation OSD (Tablet/capsules) in USFDA/UK/MHRA approved company.

Officer – Quality Control

  • Analysis of finished products, raw materials, stability samples.
  • Instrument operation and calibration knowledge.
  • Familiar with regulatory inspections (USFDA, WHO, etc.).
  • Exposure to formulation OSD (Tablet/capsules) in USFDA/UK/MHRA approved company.

Executive – Quality Control (Micro)

  • Microbial limit test validation, MIT testing.
  • Environment monitoring, water sampling and analysis.
  • Culture/biobell handling, autoclave validation.
  • Exposure to formulation OSD (Tablet/capsule) in USFDA/UK/MHRA approved company.

Executive – Quality Control

  • EMDS/LIMS specification review.
  • STP/SPEC/TOS support.
  • UMS-related CVV documentation.
  • Computer system and software validations.
  • Exposure to formulation OSD (Tablet/capsule) in USFDA/UK/MHRA approved company.

Important Note: If experience is less than 5 years, the minimum required percentage is 60%.

How to Apply

Interested candidates can apply by scanning the QR code or clicking here.

To apply for this job please visit forms.office.com.

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