Website Lupin Limited
About Lupin Limited
Lupin Limited is one of India’s leading manufacturers of bulk pharmaceutical ingredients and formulations. The primary bulk pharmaceutical ingredients produced by the company include Rifampicin, Pyrazinamide, Ethambutol (used in the treatment of tuberculosis), Cephalosporins (effective against various infections), and cardiovascular medications. Additionally, the company has expertise in phytomedicines, which involve the development of medicines derived from plant and herbal sources, supported by modern medical principles and practices.
Job Post: Associate / Jr. Officer / Officer / Executive – Production API
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
Job Post: Associate / Jr. Officer / Officer / Executive – Quality Control (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 Control (API):
- Hands-on experience with HPLC, GC, KF, IR, UV, etc.
- Lab instrument handling & troubleshooting.
- QC software proficiency: Tiamo 3.0, LIMS, QAMS, SAP, Chromeleon 7.3, etc.
- Knowledge of cGMP, Dl (ALCO+), & regulatory requirements.
- QC instrument maintenance and calibration.
Quality Control (Formulation):
- Hands-on experience with Dissolution, HPLC, KF, IR, UV, etc.
- Strong knowledge of OSD, Dry suspension formulation.
- QC software proficiency: Tiamo 3.0, LIMS, QAMS, SAP, Chromeleon 7.3, etc.
- Experience with audits like USFDA, TGA, MHRA, and other regulatory audits.
- QC instrument maintenance and calibration.
Job Post: 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 systems, investigation of OOS, OOT, OOC, risk assessment.
- Review of CSV documents, QAMS activities.
- Sampling of API finished products, review of executed documents, investigation reports, QRM, water & environmental monitoring trends.
- Review of qualification process and cleaning validation documents.
Quality Assurance (Formulation):
- Review of QC-related documents, Audit trails of computerized systems, 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 <05 years of post-qualification documented experience.
- Fresher’s need not attend the interview.
Job Location: Mandideep (Bhopal)
Walk-in Interview Dates:
- 9th September 2023 (Saturday) @ Ankleshwar (Gujarat)
- Time: 9.00 am to 5.00 pm
- Venue: Hotel Lords Plaza, GIDC, Old National Highway No. 8, Ankleshwar – 393 002
- 10th September 2023 (Sunday) @ Vadodara (Gujarat)
- Time: 9.00 am to 5.00 pm
- Venue: Baroda Productivity Council, Productivity House, 2nd Floor, BPC Road, Alkapuri, Vadodara, Gujarat
Please walk-in along with your updated resume, PP Size Photo & photocopy of all other relevant proof of qualifications and experiences. Please circulate this advertisement within your contacts, WhatsApp, Telegram, LinkedIn Group, etc.
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