Join Lupin Limited Vacancies in Quality Assurance and Control
- Vacancy in Quality at Lupin Limited
- About the Company
- Company Vacancies List
- Job Description
- Officer – Quality Assurance
- Officer – Quality Assurance
- Officer – Quality Control
- Executive – Quality Control (Micro)
- Executive – Quality Control
- How to Apply
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.