The United States Pharmacopeia (USP) is a non–governmental, official public standards–setting authority for prescription and over–the–counter medicines and other healthcare products manufactured or sold in the United States. USP also sets widely recognized standards for food ingredients and dietary supplements. USP sets standards for the quality, purity, strength, and consistency of these products–critical to the public health. USP's standards are recognized and used in more than 130 countries around the globe. These standards have helped to ensure public health throughout the world for close to 200 years.
Post: Scientist I- Reference Standards Laboratory
Job Description:
Function of the Position:
This is a non-supervisory position in Reference standard laboratory responsible for performing the required tests as a part of the project and maintaining GLP environment in the lab.
Job Responsibilities:
• Executing the analytical tests allotted by Group leader.
• Completing the project as per the timelines and trouble shoot the scientific aspects of the projects on need basis.
• Responsible for preparation of project evaluation reports.
• Responsible for sample archival and sample tracking and chemical inventory tracking in the laboratory.
• Coordination with group leader to ensure completion of the projects allotted to the team.
• Initial review of the project reports and documents and assisting the group leader.
• Responsible for preparation and review of SOP’s protocols, reports etc.
• Responsible for performing the calibration of the equipments as per the schedule.
• Responsible for preparing, executing and completing IQ/OQ/PQ of new instruments.
• Ensuring that the chemicals and column etc. are available for the projects and forward the purchase requisitions.
• Ensure all lab safety and GLP practices are maintained in the lab and participate actively in the internal and external audits and certification.
Candidate Profile: Masters degree with 2-3 years of drug quality control experience, or equivalent experience, in Chemistry, Pharmacy, or a related field.
Knowledge, Skills, Abilities:
Experience in QC laboratory, work experience under GLP and ISO environment is a plus. Working knowledge and hands on experience of common and analytical methods and procedures, and expertise in calibrating, maintaining and operating analytical instruments, such as UV, IR, HPLC, GC, Thermal analysis and wet analysis are required. Should posses excellent communication and technical writing skills.
Additional Information:
Experience: 2-3 years
Location: Hyderabad / Secunderabad
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: R&D
Last date: 25th Jan, 2013
To Apply Online Click Here
See All M.Pharm Alerts M.Sc Alerts Hyderabad Alerts
See All Other Jobs in our Database
.png)
