Vacancy at Lupin Limited, Aurangabad || Apply Now
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Click on link: https://forms.office.com/r/GgjSvh944p
Lupin Limited is one of India’s largest manufacturers with a state-of-the-art USFDA approved formulation facility at Aurangabad. We are looking for young dynamic, result oriented and committed professionals to form an integral part of our expansion.
Open Vacancy at Lupin Limited, Aurangabad
Department: Quality Assurance, Quality Control
Designation: Officer, Executive, Sr. Executive
Qualification: BSc/ MSc/ B Pharm
Experience: 3-12 Years
Details of Profile: Line clearance of manufacturing & packing area, performing in process checks at manufacturing & packing area, monitoring compliance at shop floor, issue & retrieval of
GMP documents, review of various protocols & reports, review-BMR & BPR, SOP review & preperation. Exposure to only formulation OSD (Teblet/capsules) in USFDA/ UK/ MHRA approved company.
QMMS & Documentation: Knowledge about Quality Role Handling of QAMS activities like DOS & OUT, Market Complaint, Issuance & retrieval of various GMP documents, BMR & BPR review, SOP Preparation. Quality risk assessment for product, equipment, systems, software. Change control, CAPA, intemal audit, hold time, etc. Exposure to only formulation OSO (Tablet/capsules) in USFDA/UK/MHRA approved company
Analysis of finished product/Raw materials/Stability samples, instrument operation and calibration knowledge HPLC/UV/Dissolution/IR/GC/LCMS/Malvern and its software. Familiar with regulatory inspections like USFDA, MHRA, WIHO, etc. Exposure to only formulation OSD (Tablet/capsules) in USFDA/ UK/ MHIRA approved company
Microbial limit test validation, MLT testing of Raw materials /finished product/Stability samples, packing material. Additionally Environment monitoring, water sampling and analysis, culture/bioball handling, Autoclave validation, Handling of LIMS and Vitek 2 compact or software besed identification test. Exposure to only formulation OSD (Talilet/capsules) in USFDA/UK/MHRA approved company
Reviewing EMDS/LIMS specification, STP/SPEC/TDS, Supporting LUMS related CSV documentation, Performing computer system and software validations in QC laboratory, instrument calibration/qualification, performing analysis in QC laboratory, preparation and verification of LIMS master data. Exposure to only formulation
OSD (Tablet/capsules) in USFDA/ UK/ MHRA approved company.
Important Note: If experience is less than 5 years, minimum required percentage is 60%. Candidature is not applicable if you have been interviewed in last 6 months for any Lupin location.
