Alembic Pharmaceuticals Limited Recruitment 2020 Alembic Pharmaceuticals Limited Notification full detailes below. Alembic Pharmaceuticals Limited, with an established presence in the Indian pharma industry has a proud, historical track record going back 112 years.
Important Vacancy details:
- Post Name: Analytical Method Validation/Central Validation Lab
- Education:M.pharma,B.pharma,M.sc
- Experienced:2 to 8 years
- Location:Karakhadi,Vadodara,Gujarat
- Salary: NA
- Openings:NA
- Contact:7096178090
Note:If interested candidates can share your resume to mentioned mail ID Below.
bhavana.kadam@alembic.co.in
Job Description: Hiring For Analytical Method Validation/Central Validation Lab in Alembic Pharmaceuticals Limited! If interested candidates can share your resume to mentioned mail ID bhavana.kadam@alembic.co.in
Time & Venue:19th Dec’ 2020,Time:9:30AM to 1:00PM,Venue: Alembic Pharmaceuticals,Sanskriti Hall,Opp Bhailal Amin Genaral Hospital,Vadodara,Gujarat
Pre-Planned Open Interview with Alembic Pharmaceuticals Ltd
Date : 19th Dec 2020 Saturday
Venue : Alembic Pharmaceuticals Ltd., Sanskriti Hall, Opp. Bhailal Amin General Hospital, Alembic- Gorwa, Vadodara, Gujarat – 390003.
Central Validation Lab
Designation: Executive/Senior Executive
Exp: 2-8 years
Qual: B.Sc/B.Pharm/M.Sc
- Prepare protocols and reports of Method transfer, Method verification, Method validation and Method feasibility studies.
- Hands on experience on QC instruments like HPLC,GC,KF,UV,IR. Etc
- Preparation of SOP, STPs, GTPs, specification, Record of Analysis, analysis reports, trend reports and their revision as needed.
- Preparation of protocols and summary reports of stability products.
- Investigation of OOS, OOT and Laboratory Events. •Handling of Change Control & incidents. Review of all analytical data generated at laboratory during testing.
Analytical Method Validation
Designation: Executive/Senior Executive
Exp: 2-8 years
Qual: B. Pharm/M.Sc/M.Pharm
- Perform method validation/verification/transfer activities. •
- Prepare protocols and reports of method validation/verification/transfer/feasibility studies. Hands on experience on QC instruments like HPLC,GC,KF,UV,IR. etc.
- Preparation of SOP, STPs, GTPs, specification, Record of Analysis, analysis reports, trend reports and their revision as needed.
- Preparation of protocols and summary reports of stability products.
- Investigation of OOS, OOT and Laboratory Events.
- Handling of Change Control & incidents.
Selection Process: The selection will be on the basis of Interview.
