About the Company
The firm is more than 200 years of experience in producing the quality standards helping major bio-pharmaceutical firms in delivering high quality medicines to relieve many diseases. This is an organization supplying methods at free of cost for the product development and maintaining the standards. This is distributed across the globe serving mankind.
About the Job:
Experience: 4-6 years of experience in Analytical laboratory
Qualification: MSc in analytical chemistry or Organic chemistry from a reputed university
Able to handle the Instruments like HPLC, GC, FTIR, UV-Vis, Wet chemistry and should have strong knowledge on these techniques
Broad knowledge in GMP/ GLP areas and able to perform method development and validations as and when required and document the procedures as per the Operating procedures.
Able to involve in development of synthetic organic molecules and analytical chemistry.
Need to have good technical and verbal communication skills.
Information on taking care of LCMS, GCMS and IC will be liked.
General section data Enable, ELN and NuGenesis will be liked.
Ready to discuss successfully with both inward and outside clients. Ideally acquainted with electronic journal documentation of trial methods.
Great relational abilities and demonstrated capacity to work in a group situated climate are essential.
What will YOU make mean for here at USP?
Backing to conclusive examination of tests according to monograph/in-house techniques. Plan insightful test reports for Engineered projects (USPNF and PAI). Execute projects per the supported test conventions whenever alloted.
Liable for arrangement of SOPs, conventions, reports, and so on. Guarantee the tasks necessities by organizing with the Buying division. Liable for arrangement of the records and archives. Guarantee that the alignments of the gear's are proceeded according to the timetable
Plan, execute, and complete intelligence level/OQ/PQ of new instruments. Indent the expected glass product, synthetic substances, and sections for the ARD projects. Keep up with GLP and carry out wellbeing methodology while working in Lab. Perform different Undertakings at whatever point liberated from ARD exercises. Perform different obligations as alloted
Readiness and making arrangements for ISO-9001 confirmation/recertification by partaking effectively, check of conventions and related reports and play a functioning job in the interior as well as outer QA reviews and address the review issues as soon a possible. Taking up some other extra obligations relegated by manager on a proactive premise and dispensing extra liabilities to the revealing staff in meeting with the boss. Takes part in USP cross-practical groups as suitable.
Practice Variety, Value, Incorporation, and Having a place standards at USP India.