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.We have spent last two decades in building up our scientific and technological capabilities, research, and manufacturing competencies.Â
- Vacancy details:
- Role: Â Production/ Instrumentation/ Maintenance Â
- Qualification : M.Sc. Chemistry/Â B.Tech Chemical
- Experience : 2 to 8 years in API Industry only
- Salary:  ₹Not Disclosed
Greetings from Ami Lifesciences Ltd..!!!!
- Important Details :
- Location: Vadodara
- Post of date:03/08/2024
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: face to face
- Interview Rounds of Interview: HR
Walkin Interview Details:
Date: 10th Aug 2024 (Saturday)
Time: 10:00 am to 4:00 pm
Venue: Productivity House, 4th Floor, BPC Rd, Alkapuri, Vadodara, Gujarat 390007

1) Department:Â Production
Eligibility:Â M.Sc. Chemistry/Â B.Tech Chemical
2 to 7 years of experience in API Industry
Skills:Â
API Production, Bulk Drug
Batch start-up activity, monitoring
Calibration of balance
Review technical documents like batch records, SOPs, BMR, validation protocols, etc.
Knowledge and exposure of cGMP is must.
2) Department:Â Engineering (Instrumentation)
Eligibility:Â B.Tech Instrumentation Engineering
2 to 6 years of experience in API Industry
Skills:Â
Maintaining, calibrating, and troubleshooting instrumentation and control systems.
Preparation of SOPs, DQ, IQ, OQ, and other documentation.
Ensuring accurate process measurements and compliance with GMP standards.
Must possess strong analytical skills and hands-on experience with automation systems.
3) Department:Â Engineering (Maintenance)
Eligibility:B.Tech Mechanical Engineering
2 to 6 years of experience in API Industry
Skills:Â
Perform preventive and corrective maintenance on mechanical equipment.
Ensuring minimal downtime, and adhering to safety and compliance standards.
Must have strong troubleshooting skills and experience with GMP practices and documentation.

