Hiring for Lupin Limited – Mandideep, Bhopal (MP) for API & Formulation
(Hiring for multiple positions)
Associate/ Jr. Officer / Officer / Executive – Production API
MANDIDEEP (Bhopal)
Experience: 2 to 8 Years
(in Regulatory Pharma Co. only)
Education: Regular Course only-Diploma Chemical/B.Sc. (Chemistry)/ M.Sc. (Chemistry)
Job Description:
Shift Production -FPP area in charge
Solvent Recovery Area In charge
Associate/ Jr. Officer/ Officer /Executive – Quality Control (API & Formulation)
Experience: 1 to 8 Years
(in Regulatory Pharma Co, only)
Education:
Regular Course only B.Sc. (Chemistry)/ M.Sc. (Chemistry)/B.Pharma
Quality Control
API
•Hands on experience with HPLC, GC, KF, IR, UV etc.
•Good exposure in lab instruments handling & trouble shooting.
•Hands on experience of QC software like Tiamo 3.0, LIMS, QAMS, SAP, Chromeleon 7.3 etc.
•Aware of cGMP, DI (ALCO+) & various regulatory requirements
•QC Instrument maintenance and calibration.
Formulation
•Hands on experience on Dissolution, HPLC, KF, IR, UV etc.
•Strong knowledge for OSD, Dry suspension formulation.
•Hands on experience of QC software like Tiamo 3.0, LIMS, QAMS, SAP, Chromeleon 7.3 etc.
•Experience of facing audits like USFDA, TGA, MHRA & other regulatory audits
•QC Instrument maintenance and calibration.
Associate / Jr. Officer /Officer / Executive – Quality Assurance (API & Formulation)
Experience:
2 to 8 Years (in Regulatory Pharma Co. only)
Education:
Regular Course only-B.Sc
(Chemistry)/ M.Sc. (Chemistry)/B. Pharma
Quality Assurance
API
•Review of QC related documents, Audit trails of computerized system, investigation of OOS, OOT, OOC, risk assessment.
•Review of CSV documents, QAMS activities
•Sampling of API finished products, review of executed documents, investigation report, QRM, water & environmental monitoring trend
•Review of qualification process and cleaning validation documents.
Formulation
•Review of QC related documents, Audit trails of computerized system, investigation of OOS, OOT, OOC, risk assessment.
•Handling IPQA activities, review for Oral Dosage form.
•Handling qualification and validation of Formulation Facility.
•Review of qualification process and cleaning validation documents.
Preferences/Compulsion:
•Relevant exposure in API/Pharma Formulation/Bulk Drug /Pharma Industries 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 co5 years of post qualification documented experience.
•Fresher’s need not attend the interview.
Date: 9th September 2023 (Saturday)
Time: 9.00 am to 5.00 pm
Venue:
Hotel Lords Plaza, Lords Plaza
GIDC, Old National Highway No. 8 Ankleshwar -393 002
Date: 10th September 2023 (Sunday)
Time: 9.00 am to 5.00 pm
Venue:
Baroda Productivity Council, Productivity House, 2″ Floor, BPC Road,
Alkapuri, Vadodara, Gujarat
Please walk-in along with your updated resume, PP Size Photo & photo copy of all other relevant proof of qualifications and experiences.
Please circulate this advertisement with your all contacts related WhatsApp, Telegram, Linkedin Group etc.
