Over the years, Lupin has grown and expanded into new areas and regions, manufacturing drugs that extend the promise of good health to communities across the globe. Beginning with two employees a peon-cum-packer and a part-time typist Lupin’s current global footprint spans 11 countries, across six continents. This journey has been made possible thanks to the vision and conviction of Dr. Desh Bandhu Gupta.
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Quality Control (Hormonal – OC / HPD)
Qualification & Experience : Officer / Executive (B. Pharma/ M.sc)
Min 2 to 6 Years for Officer
Min 8 to 10 years Executive
Job Profile : Knowledge of HPLC/GC /LCMS/ICPMS and others routine instruments of QC and work experience with regulatory compliance organizations (US FDA/EU etc.) Analysis of formulation and stability samples tablets dosage. (In-process/ /BU/CU/Assay/Dissolution/RS/OVI) RM/FP/SS, OOS and OOT handling and report writing, Handling of laboratory deviation. Understanding of laboratory instrument software validation and 21 CFR. Analysis of API, intermediate and Raw materials. Knowledge of GLP Section, understanding of laboratory instruments Qualification/Calibrations. Good Knowledge of Analytical method transfer /Method validation/cleaning validation and Pharmacopeia updates.
Quality Control (Service Engineer)
Qualification & Experience : Executive (Any Graduate) Min 8 to 10 years
Job Profile : Maintenance & calibration of lab instruments (HPLC, GC, UV, etc.) Equipment troubleshooting & vendor coordination. Documentation & compliance with GMP/GLP standards. Support audits and train QC analysts. Hands-on experience with pharma QC equipment. Strong understanding of regulatory guidelines. Excellent problem-solving and communication skills.
Quality Assurance (API)
Qualification & Experience : Officer (B. Pharma/ M.sc) Min 2 to 6 Years
Job Profile : Monitor shop floor activities and ensure compliance. Prepare and review SOPs, master documents, and validation protocols. Handle investigations (OOS, OOT, deviations, complaints) with CAPA. Review equipment cleaning records, stability reports, and APQR Participate in risk assessments, regulatory submissions, and QA documentation. Ensure in- process QA during production and sampling stages
Quality Assurance (API)
Qualification & Experience : Executive (B. Pharma) (8 to 10Years)
Job Profile : SOP preparation & review. Quality Risk Assessment. Validation & Qualification document review. Handling deviations, CAPA, OOS/OOT. In-process QA & shop-floor monitoring. SAP UD/release activities.
QA Validation (API)
Qualification & Experience : Officer (B. Pharma) (2 to 6Years)
Job Profile : Cleaning Validation: Handle protocol/report preparation, acceptance criteria, and tracking of cleaning verification activities. Equipment Qualification: Prepare, review, and execute FAT, IQ, OQ, PQ; review URS, DQ, SAT, and vendor documents. HVAC & Utility Qualification: Execute and document qualifications for AHUs, HEPA filters, water, steam, compressed air, nitrogen, etc. Packaging Validation: Conduct and document packaging validation activities including data compilation and report preparation. Facility Qualification: Manage facility qualification tasks and related documentation. Cross-Functional Coordination: Collaborate with QA, QC, Engineering, Production, and external vendors for validation activities. Documentation: Prepare/review SOPs, Validation Master Plans, study protocols/reports, and qualification status labels.
Quality Control (MDI / DPI)
Qualification & Experience : Officer (B. Pharma/ M.sc) Min 2 to 6 Years
Job Profile : Analysis of Finished product samples. i.e., Aerosol Products (MDI/DPI). To maintain the instrument usage and maintenance of instruments like UV spectrophotometer, HPLC, GC, Analytical Balance, PH meter, Spray View etc. Having Analytical testing skills to perform the MDI/DPI Products test like Assay, APSD by NGI, DDU, RS, Spray Pattern, FPM, and physical testing etc. Knowledge of HPLC/GC (Chromeleon software) and others routine instruments of QC. Understanding of Data Integrity, GMP, laboratory instrument software 21 CFR
Quality Control (Nasal / Derma)
Qualification & Experience : Officer (B. Pharma/ M.sc) Min 2 to 6 Years
Job Profile : Analysis of Finished product samples Nasal & Derma formulation. To maintain the instrument usage and maintenance of instruments like UV spectrophotometer, HPLC, GC, Analytical Balance, PH meter, Spray View, Spray Tech etc. Having Analytical testing skills to perform the test like Assay, SCU, RS, Spray Pattern, DSD, FPM and physical testing etc. Knowledge of HPLC/GC (Chromeleon software) and others routine instruments of QC. Understanding of Data Integrity, GMP, laboratory instrument software 21 CFR.
Quality Assurance (Sterile)
Qualification & Experience : Executive (M.sc Micro) Min 8 to 10 Years
Job Profile : Batch Record Review – Review BMRs/BPRs for sterile products. Environmental monitoring in Aseptic Area. Aseptic practices monitoring in sterile area. Review of qualification documents like Autoclave, media fill, smoke studies, CCIT, SIP validation, visual inspection qualification and other Equipment related o sterile operations. Review of Electronic data. Line Clearance – Perform line clearance for manufacturing and packing areas. Documentation – Prepare/review SOPs, protocols, and QA reports. Compliance – Handle deviations, change controls, CAPAs, and ensure timely closure. Audit Support – Assist in internal/external audits and regulatory inspections.
Validation (Sterile)
Qualification & Experience : Officer (B. Pharma) Min 2 to 6 Years
Job Profile : Cleaning Validation – Prepare protocols/reports, set acceptance criteria, and track verification activities. Equipment Qualification – Execute FAT, IQ, OQ, PQ; review URS, DQ, SAT, and vendor documents. Autoclave qualification, media fill, smoke studies, CCIT, SIP validation, visual inspection qualification and qualification of other Equipment related o sterile operations. HVAC & Utility Qualification – Qualify AHUs, HEPA filters, water systems, steam, compressed air, nitrogen. Facility Qualification – Manage facility qualification tasks and documentation. Documentation – Prepare/review SOPs, Validation Master Plans, protocols, reports, and status labels. Compliance & QMS – Handle change controls, deviations, CAPAs, and ensure adherence to SOPs and timelines. Computer system validation
Microbiology (Sterile)
Qualification & Experience : Officer (M.sc Micro)
Min 2 to 6 Years
Job Profile : Perform Environmental Monitoring in sterile areas (air, surface, personnel). Conduct Sterility Testing, Endotoxin Testing, and Water Analysis. Prepare and qualify media, perform Growth Promotion Testing, and maintain cultures. Review and maintain SOPs, logbooks, and EM reports. Support investigations, deviations, and CAPAs related to microbiology. Ensure compliance with cGMP, GDP, and EHS guidelines. Supports in qualification of the Equipment like Autoclave, incubators and other instruments used in the Microbiology lab.
Production (Ophthalmic)
Qualification & Experience : Associate - Controlled Area (ITI / D. Pharma / B.Sc) (2 to 8 Years)
Job Profile : Hands-on experience in cleanroom operations and GMP documentation. Skilled in steam sterilizer load prep, equipment operation, cleaning, and troubleshooting. Proficient with vessels, sterilizers, homogenizers, CIP/SIP, filter integrity, and glove leak testing. Accurate recording of process parameters in BMRs and logbooks. Balance calibration, material issuance, and in- process checks. Expertise in bulk manufacturing and filtration in controlled environments.
Production (Ophthalmic)
Qualification & Experience : Associate - Aseptic area (ITI / D. Pharma / B.Sc) (2 to 8 Years)
Job Profile : Skilled in aseptic operations, sterile API handling, and suspension manufacturing. Operated and maintained filling machines (e.g., Romaco), vessels, dyno mill, and homogenizers. Performed cleaning, troubleshooting, and in-process checks as per BMR. Handled laminar air flows, pass boxes, garment cubicles, and NVPC systems. Maintained accurate documentation in BMRs and logbooks. Conducted balance calibration, material issuance, and followed aseptic practices
Production (Hormonal – OC / HPD)
Qualification & Experience : Associate (ITI / D. Pharma / B.Sc) (2 to 8 Years)
Job Profile : Experience in Granulation machine operation. TRV machine (Turbo Rapid variable Drive) Make : Gea, Flow wrap machine operation. Experience in Fette compression machine operation (Preferably Fette 3200i model)
Production (Hormonal – OC / HPD)
Qualification & Experience : Officer (B. Pharma) (2 to 6 Years)
Job Profile : Knowledge on Granulation M/C. Knowledge on Compression M/C Fette 3200i. Knowledge of SAP & Documentation related to Production.
Packing (Hormonal – OC / HPD)
Qualification & Experience : Associate (ITI / D. Pharma / B.Sc) (2 to 8 Years)
Job Profile : Responsible for operating & troubleshooting of Bottle Packing Line of following primary machines. Countec Make machines of primary bottle packing area (e.g. machines like Counting Machine, Rotary capping Machine, Silica Inserter m/c, Stabilox inserter, Checkweigher & Metal Detector etc. Performing challenge tests & in-process of primary bottle packing line, Good knowledge of cGMP & GDP.
Production (Hormonal – OC)
Qualification & Experience : Executive (B.Pharma) (8 to 10 Years)
Job Profile : Handling of QAMS & Documentation related to Production. Knowledge of shop floor process of Production area. Knowledge of SAP application related to Production. Investigation writing skills & use of root cause analysis tools.
Production (Derma / Nasal)
Qualification & Experience : Associate (ITI / D.Pharma / B.Sc) (2 to 8 Years)
Job Profile : Operate the Filling activity for Nasal / Topical Formulation. Knowledge of filling equipment like Derma / Nasal filling machine i.e. Bottle filling and capping machine (Make: PKB), Sofbag filling machine (Make: Marchesini), Tube Filling Machine (Make: NORDEN and IMA-PG)
Production (Derma / Nasal)
Qualification & Experience : Officer / Executive (B. Pharma) Min 2 to 6 Years for Officer Min 8 to 10 years Executive
Job Profile : Supervise the Manufacturing, Filling activity for Derma & Nasal Formulation. Knowledge on filling equipment’s like Master plant 1000kg (make: ADAM) Filling machine i.e. Bottle filling and capping machine (Make: PKB), Sofbag filling machine (Make: Marchesini), Tube Filling Machine (Make: NORDEN and IMA-PG), Nasal filling machine (Make: DARA). Oversee the Manufacturing and filling process of pharmaceutical products, ensuring accuracy and efficiency.
** USFDA & MHRA regulatory exposure is Mandatory.
Walk in Interview
Date : 8th November 2025
Venue : Lupin Limited Pithampur, Madhya Pradesh
Email ID : parichayindore@lupin.com
Prerequisites for Interview :
- Relieving letters from all previous organization.
- Must not be interviewed at Lupin in last six months.
- 60% marks is mandatory in case of experience is less then 5 Years.
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