Lupin Pharmaceutical Ltd.(Aurangabad)
Vacancy Details :-
1) Associate/ Officer - PRODUCTION
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.
2) Executive/ Officer Quality Assurance
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 & 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.
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Important Details :-
Job Location :- Aurangabad
Interview Date :- 24th December 2023 (Sunday)
Interview Time :- 9.30 am to 4.00 pm
Interview Location :- Regenta Central Antarim Hotel Between Girish Coldrink & St. Xaviers Corner, Chimanlal Girdharial Rd, Navrangpura, Ahmedabad, Gujarat 380006
