LUPIN – Mega Walk-In Drive for B.Sc, M.Sc, B.Pharm, D.Pharm, ITI Candidates in Production / QA / QC on 24th Dec’ 2023

• Interview Date: 24th December 2023 (Sunday)
• Interview Time: 9.30 am to 4:00 PM
• Venue-Regenta Central Antarim Hotel – Ahmedabad

• Experience – 2 to 7 Years
• Education-ITI/BSc./D Pharm/B. Pharma
• Job Description: Experience of Compression operations. Hands on equipment experience for tablet manufacturing, RMG/FBD/CADMACH Mark, HATA/ Killian/Coating machine. Exposure to only formulation OSD (Tablet/capsules) in USFDA/UK/MIIRA approved company.

• Experience – 3 to 7 Years
• Education-B.Pharma
• Job Description: 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 & BIPR, SOP review & preparation. Exposure to only formulation OSD (Tablet/capsules) in USFDA/UK/MHRA approved company.

• Experience-3 to 7 Years
• Education-B.Pharma
• Job Description: QMS & Documentation. Knowledge about Quality Role-Handling of QAMS activities like 005 & OCT, Market Complaint, Issuance & retrieval of various GMP documents, BMR & BPR review, SOP Preparation. Quality risk assessment for product, equipment, systems, software. Change control, CAIPA, internal audit, hold time, etc. Exposure to only formulation OSD (Tablet/capsules) in USFDA/UK/ MHRA approved company.

• Experience 2 to 10 Years
• Education-B.Sc./MSc/B. Pharm
• Job Description: 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 USFOA, MHRA, WHO, etc. Exposure to only formulation OSD (Tablet/capsules) in USFDA/UK/MHRA approved company.

• Experience – 12 to 15 Years
• Education-B.Sc./MSc/B. Pharm
• Job Description: Reviewing EMDS/LIMS specification, SIIP/SPEC/10S, Supporting LIMS related CSV documentation, Performing computer system and software validations in QC laboratory, Instrument calibration/qualification, performing analysts in QC laboratory, preparation and verification of LIMS master data. Exposure to only formulation OSD (lablet/capsules) in USFDA/UK/MHRA approved company.

• Relevant exposure in Pharmaceutical Industries-05D Formulation with process safety implementation, Excellent Communication &  Interpersonal Skills.
• Candidate should be dedicated and disciplined.
• Must have scored 60% marks/1st class in their highest qualification, if having <05 years of post qualification documented experience.
• Fresher’s need not attend the interview.

• Date: 24th December 2023 (Sunday)
• Time: 9.30 am to 4.00 pm
• Venue – Regenta Central Antarim Hotel, Between Girish Coldrink & St. Xaviers Corner, Chimanlal Girdharlal Rd, Navrangpura, Ahmedabad, Gujarat 380006

 

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