Lupin Limited-Opening for B.Pharm, MSc, BSc in QA, QC
Lupin Limited is one of India’s largest manufacturers of bulk actives and formulations. The principal bulk actives manufactured by it include Rifampicin, Pyrazinamide, Ethambutol (anti-TB), Cephalosporins (anti-infectives) and cardiovasculars. The company also possesses competencies in phytomedicines, in which medicines are made out of plant and herbal resources supported by the discipline of modern medicine.
Quality Assurance – Officer
Qualification : B.Pharma
Experience : 3-7 Years
Details of Profile : Line clearance of manufacturing ft packing area, performing in process checks at manufacturing ft packing area, monitoring compliance at shop floor, issue & retrieval of GMP documents, review of various protocols & reports, review-BMR & BPR, SOP review & preparation. Exposure to only formulation OSD (Tablet / capsules) in USFDA / UK / MHRA approved company.
Quality Assurance – Officer
Qualification : B. Pharma
Experience : 3 – 7 Years
Details of Profile : QMS & Documentation : Knowledge about Quality Role – Handling of QAMS activities like OOS & OOT, Market Complaint, Issuance & retrieval of various GMP documents, BMR & BPR review, SOP Preparation. Quality risk assessment for product, equipment, systems, software. Change control, CAPA, internal audit, hold time, etc. Exposure to only formulation OSD (Tablet / capsules) in USFDA / UK / MHRA approved company.
Quality Control – Officer
Qualification : B.Sc./MSc/B. Pharm
Experience : 3- 5 Years
Details of Profile : 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, WHO, etc. Exposure to only formulation OSD (Tablet / capsules) in USFDA / UK / MHRA approved company.
Quality Control – Executive
Qualification : MSc Micro
Experience : 4 – 8 years
Details of Profile : 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 based identification test. Exposure to only formulation OSD (Tablet / capsules) in USFDA / UK / MHRA approved company.
Quality Control – Sr. Executive
Qualification : B.Sc./ MSc / B.Pharm
Experience : 8-12 Years
Details of Profile : Reviewing EMDS / UMS specification, STP / SPEC / IDS, Supporting LIMS related CSV documentation, Performing computer system and software validations in QC laboratory, Instrument calibration / qualification, performing analysis in QC laboratory, preparation and verification of UMS master data. Exposure to only formulation OSD (Tablet / capsules) in USFDA / UK / MHRA approved company.
Job Location : Aurangabad, Maharashtra