Lupin Pharma Walk In Interview For Diploma Chemical/ BSc/ MSc Chemistry/ B Pharm- QA/ QC/ Production

Lupin Pharma Walk In Interview Details:

Date: 9th September 2023 (Saturday)

Time: 9.00 am to 5.00 pm

Venue: Hotel Lords Plaza, Lords Plaza GIDC, Old National Highway No. S 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

1) Associate/ Jr. Officer / Officer / Executive – Production API

• Experience – 2 to 8 Years (in Regulatory Pharma Company only)
• Education – Regular Course only Diploma Chemical/ B.Sc. (Chemistry)/ M.Sc. (Chemistry)

2) Associate / Jr. Officer/ Officer / Executive – Quality Control (API & Formulation)

• Experience: 2 to 8 Years ( Regulatory Pharma Co. only)
• Education- Regular Course only B.Sc. (Chemistry)/ M.Sc. (Chemistry)/ B.Pharma

A) 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

B) Quality Control – 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.

3) Associate / Jr. Officer / Officer / Executive – Quality Assurance (API & Formulation)

• Experience- 1 to 8 Years (Regulatory Pharma Co. only)
• Education- Regular Course only-B.Sc. (Chemistry)/ M.Sc. (Chemistry)/ B. Pharma

A) Quality Assurance – API

• Review of QC related documents, Audit trails of computerized system, investigation of 00S, 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

B) Quality Assurance – Formulation

• Review of QC related documents, Audit trails of computerized system, investigation of 00S, 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