Ami Lifesciences Ltd Walk-in Interview Details Below .Ami Lifesciences was founded 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. Along the way we have earned a reputation for being innovative, inventive and resourceful.
- Vacancy details:
- Department: Production / Quality Control : Officer – Executive
- Qualification: B.Tech/B.E. in Chemical/MS/M.Sc(Science) in Organic Chemistry
- Experience: 2 – 7 years
Greetings from Ami Lifesciences Ltd..!!!!
Important Details :
- Location: Vadodara
- Post of date:11/11/2024
- 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: 16th November
Time: 10.00 AM – 4.00 PM
Venue:2nd Floor, Productivity House, Baroda Productivity Road, Alkapuri, Vadodara – 390007
Production – Officer / Executive :
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 production,
To be responsible for receiving raw materials to delivering the finished products.
Quality Control – Officer / Executive :
Attending regulatory and customer audits.
Preparation and implementation of SOPs as per regulatory requirements.
Evaluating training needs of teams & conducting GMP, GLP & other training programs for employees across levels & functions.
Conducting basic GMP, refreshing/updating GMP training to all company employees.
Supervising the quality audit process for RM & PM vendors, contract manufacturing sites & third-party sites.
Preparing sample management system for control, validation, stability & market/customer samples
Overseeing dossier preparation and filing, planning, preparation, review, and evaluation of related documents
