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Research Scientist
Contract : Irvine, California, US
Salary Range : 40.00 - 52.00 | Per Hour
Job Code : 359214
End Date : 2025-03-26
Days Left : 28 days, 2 hours left
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Position Details :
Industry : Pharmaceutical / Medical Devices
Job Title : Research Scientist (Chemist III) - Onsite
Location : Irvine, CA 92612
Duration : 12 months [ Possibilities of extension]
Pay Range : $45-$52 / hr
Purpose :
The ideal candidate is expected to maintain current knowledge and understanding of GMP requirements and practices, familiar with analytical techniques such as HPLC / UPLC with various detectors such as CAD, RI, UV / PDA, GC-FID , particle size distribution, physical appearance, pH meter, turbidimeter, osmometer, viscosity, rheometry and drug delivery system release profiles for drug products and / or drug substances.
Upon assignment, independently plans and conducts analytical chemistry analyses in a timely and efficient manner and ensures data integrity and accuracy.Prompt and accurate documentation of experiments, results and conclusions are important responsibilities.Ensures laboratory operational capability by proper maintenance of laboratory equipment and instrumentation.Obtain necessary chemical reagents, reference standards and other components from appropriate sources.The candidate must have proactive, cross functional communication skills.Participate, collaborate and contribute at group and project meetings as required.Provides training to peers to enhance their work effectiveness in generating analytical data.The candidate independently compiles, evaluates, and / or statistically analyzes technical data.With limited supervisor input, design, plan, and perform a variety of project-oriented analytical work assignments (e.g., maintain the integrity of the stability testing program and respective stability data, analyze samples, perform method qualification / validation, and analyze / record / report results and conclusions of experiments).Additionally, the candidate must be proactive in critically interpreting data and learning new techniques. Under supervision, develop analytical methods and prepare method documents, prepare stability protocols / reports, prepare method validation protocols / reports, draft technical memos / reports and support regulatory submissions.A working knowledge of phase appropriate analytical development (methods, validation, and stability program) is preferred. The candidate must conduct their work activities in compliance with all company internal requirements and with applicable regulatory requirements. Company internal requirements include compliance with ethics, environmental health and safety, financial, human resources and general business policies, requirements, and objectives.Top 5 Skills Required :
Analytical techniques such as GC / HPLC / UPLC with various detectors such as CAD, RI, UV / PDA, GC-FID, particle size distribution, physical appearance, pH meter, turbidimeter, osmometer, viscosity, and rheometry.Maintain current knowledge and understanding of GMP requirements and practicesDocumentation of experiments, results and conclusions.Compiles, evaluates, statistically analyzes, and present technical data.M.S. in Analytical Chemistry or related discipline with minimum 2 years of experience or B.S. in Analytical Chemistry or related discipline with minimum 5 years of experience in analysis of pharmaceutical products or pharmaceutical method development and validation.Job Requirement
Supplier QualitySupplier ManagementVendor ManagementSupplier change noticeSupplier's ManagementThird Party ManufacturingMedical DeviceMedical DevicesReach Out to a Recruiter
RecruiterEmailPhoneNiharika Shrivastavaniharika.shrivastava@collabera.comApply Now
Salary : $45 - $52
