Lupin Limited is one of India's largest manufacturers of bulk actives and formulations. The principal bulk actives manufactured by it include Rifampicin, Pyrazinamide, Ethambutol (anti-TB), Cephalosporins (anti-infectives) and cardiovasculars. The company also possesses competencies in phytomedicines, in which medicines are made out of plant and herbal resources supported by the discipline of modern medicine.
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
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.
• 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, Dl (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 <05 years of post qualification documented experience.
• Fresher’s need not attend the interview.
Job Location : Mandideep (Bhopal)
9th September 2023 (Saturday) - Walk-in Interview @ Ankleshwar (Gujarat)
Time : 9.00 am to 5.00 pm
Venue - Hotel Lords Plaza, Lords Plaza
GIDC, Old National Highway No. 8
Ankleshwar -393 002
10th September 2023 (Sunday) - Walk-in Interview @ 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 & 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.
See All B.Pharm Alerts M.Pharm Alerts Ph.D Alerts M.Sc Alerts
See All Other Jobs in our Database
.png)
