Ami Lifesciences Ltd Walk In Interview 2023/Ami Lifesciences Ltd Notification full details below. Interested and eligible candidates can attend Interview on scheduled time and venue.Ami Lifesciences was incorporated with the goal of changing the way in which quality medicines are delivered to people in need. We operate on the principle by extending our focus and services to maximize our impact on the global pharmaceutical industry.
Vacancy details:
- Department: Production
- Post Name: Chemist / Officer/ Executive
- Qualification: B.Sc in Any Specialization, B.Tech/B.E. in Any Specialization/MS/M.Sc(Science) in Any Specialization, M.Pharma in Any Specialization, M.Tech in Any Specialization
- Experienced: 02-07+years
- Salary: 3.5-6.5 Lacs P.A.
Job Description: Greeting from Ami Lifesciences Ltd !!!
Important Details :
- Location: Vadodara/ Baroda,Gujarat
- Post of date:13/09/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to Face interview
- Interview Rounds of Interview: HR
Walk-in Interview Details
17th September , 9.30 AM – 5.30 PM
Productivity House, 2nd Floor, BPD Rd, Alkapuri, Vadodara, Gujarat
Contact – Aparna Mishra/Yogita Sidhwani
Roles and Responsibilities
- API Production, Bulk Drug,API Production
- To be responsible for Batch start up activity, monitoring, calibration of balance and other instruction given by the Superior,
- To review technical documents like batch records, cleaning records, validation protocols, cleaning verification protocols,
- SOPs, cGMP, Reactor, BMR Review, Raw Material, Hydrogenation, batch
Desired Candidate Profile
- Candidate with exposure in API Production must
- Qualification: M.Sc.Chemistry / BE / B.Tech Chemical
- Experience: 2 to 5 years in API Industry only
Role & responsibilities
- Responsible for production as per received plan and align for necessary equipment, raw material, and manpower with concerned departments.
- Responsible for allocation of Manpower and distribution of work.
- Submission of Daily Production Report in determined format (Input-Output Data, WIP, Stock Statement)
- Monitoring and ensuring cGMP activities and adhering to QMS.
- Planning and ensuring proper documentation like Change Control, CAPA, BPCR, OOS, OOT reports, internal and external audit compliance reports, etc.
- Planning of Preventive Maintenance, Breakdown Maintenance of equipment with line clearance.
Preferred candidate profile
- Candidate must posses BE/B.tech in chemical.
- Experience: 4 to 8 years of experience in Pharmaceuticals, API In pilot plant
