April 21, 2024

Hiring for Lupin Ltd Mega Walk-in Drive 24th Dec 2023 for Multiple Positions

Education-ITI/ BSc/ D Pharm/ B. Pharma

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.

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 & BIR, SOP review & preparation. Exposure to only formulation OSD (Tablet/ capsules) in USFDA/ UK/ MHRA approved company.

3) Executive/ Officer Quality Assurance

Experience 3 to 7 Years

Education-B. Pharma

Job Description:

QMS & Documentation. Knowledge about Quality Role-Handling of QAMS activities like 005 & 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 (lablet/ capsules) in USFDA/UK/ MI IRA approved company.

4) Executive Officer – Quality Control

Experience 2 to 10 Years

Education-B.Sc./ MSc/ B. Pharm

Job Description:

Analysis of finished product/Kaw 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.

5) Sr. Executive Quality Control

Experience-12 to 15 Years

Education-B.Sc./ MSc/ B. Pharm

Job Description:

Reviewing EMDS/ LIMS specification, SIIP/ 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 LIMS master data. Exposure to only formulation OSD (tablet/capsules) in USFDA/ UK/ MHRA approved company.

Preferences/Compulsion:

Relevant exposure in Pharmaceutical Industries-OSD Formulation with process safety implementation, Excellent Communication S

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.

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 Girdharial Rd, Navrangpura, Ahmedabad, Gujarat 380006

Please walk-in along with your updated resume, copy of Aadhar card and Pan card, PP Size Photo & photo copy of all other relevant proof of qualifications and experiences.

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