Ipca Laboratories Walk-In Interview for Various Positions (2nd June 2024)
🔬 About Company:
Ipca Laboratories Limited, headquartered in Mumbai, India, is a global pharmaceutical company involved in the production, promotion, and distribution of APIs, pharmaceutical formulations, and medicinal products. Known for its strong global presence, Ipca is recognized as one of the leading manufacturers of more than twelve APIs worldwide.
📝 Job Details:
- Position: Production, Packing, Warehouse, Engineering
- Organization: Ipca Laboratories Ltd.
- Qualification: 12th, Diploma, B.Sc, M.Sc, B.Pharm, M.Pharm, BE, B.Tech
- Experience: 3-10 years
- Location: Ratlam (M.P.)
📅 Walk-in Interview Details:
- Date: 2nd June 2024 (Sunday)
- Time: 10:00 AM – 5:00 PM
- Venue: Papaya Tree Hotel, Near Dr. Hardia Eye Clinic, AB Road, RAU, Indore (M.P.)
- Contact: Himanshu Banerjee
🔍 Vacancy Details:
Department | Designation | Qualification | Experience |
---|---|---|---|
Engineering (Formulation) | Officer/Senior Officer | BE/B.Tech/Diploma (Mechanical/Electrical & Instrumentation) | 3-10 years |
Quality Control (Formulation) | Executive (Micro) / Officer/ Sr. Officer/ Freshers | 12th/ITI/Non-Science Graduate/B.Sc (only for Micro) | Freshers/ 2-5 years |
Formulation Injection/ Injectable/ Tablet | Chemist/ Officer/ Executive | M.Sc./ M.Pharma /B.Sc./ B.Pharma/ D.Pharma | 3-10 years |
QA & Lab QA (Formulation) | Officer/ Sr. Officer/ Executive | B.Sc./M.Sc./ B.Pharma/ M.Pharma | 3-10 years |
📝 Job Descriptions:
- Engineering (Formulation):
- Handle maintenance and troubleshooting of formulation equipment.
- Experience with vial & ampoule line equipment for injectable facilities.
- Knowledge in documentation like DQ, IQ, OQ.
- Quality Control (Formulation):
- Analyze formulation products (Injection, Tablet, Dry Syrup, Liquid).
- Exposure to instruments like HPLC, GC, UV, IR.
- Experience in microbiology lab, sterility tests, bacterial endotoxin test, and environmental monitoring.
- Formulation Injection/ Injectable/ Tablet:
- Operate machines for tablet manufacturing and sterile area production.
- Handle documentation, BMR, BPR E-Log Book.
- Supervise batch manufacturing, filling, labeling, cartoning, and validation activities.
- QA & Lab QA (Formulation):
- Experience in IPQA, validation, stability studies, regulatory affairs, and QA documentation.
- Exposure to QMS, deviation, CAPA, and Trackwise system.
📄 Important Details:
Documents to Carry:
- Aadhar Card
- Salary slips of the last 3 months
- CTC structure
📧 Contact Emails:
- Himanshu Banerjee: Himanshu.banerjee@ipca.com
- Shivani Verma: Shivani.verma@ipca.com