Herbalife Nutrition
Overview
THE ROLE:
The Analytical Scientist I will be expected to develop and validate new analytical methods with minimum to no supervision as well as to provide technical support to other corporate groups including Research and Development and Global Licensing.
HOW YOU WOULD CONTRIBUTE:
Develop and validate new analytical methods
Design and execute method transfer protocols
Generate, write and revise SOPs, test methods, validation protocols and validation reports
Mentor chemists/analysts in the proper execution, including interpretation of validation parameters
Provide technical support to the analytical methods used for marketed products by QC lab and products in development phase
Achieve and maintain high standards with meticulous attention to detail
Conduct laboratory investigation activities
Troubleshoot different analytical instruments
Lead method development projects
Serve as technical lead for specific area of expertise
Assist Analytical Scientist III or Sr. Scientist in drafting publication or position papers
Interpret test results and compare with determined standards and limits.
Interpret and compare data to historical records and verifies trending
Take active role to ensure the laboratory is in compliance with cGMP and GDP
Assist in audit and compliance program to meet ISO17025 laboratory accreditation requirements (including statistical analysis of data)
Assist in drafting publication or position papers
Qualifications SKILLS AND BACKGROUND REQUIRED TO BE SUCCESSFUL:
Solid knowledge of cGMP and GDP
Well versed with various data acquisition/processing software and other laboratory controls
Highly proficient in most of lab instrumentation (i.e. FTIR, HPLC, ICP, GC, UV-Vis, LC-MS, GC-MS, ICP-MS, HPTLC) and test methods
Strong analytical and problem solving ability
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The Analytical Scientist I will be expected to develop and validate new analytical methods with minimum to no supervision as well as to provide technical support to other corporate groups including Research and Development and Global Licensing.
HOW YOU WOULD CONTRIBUTE:
Develop and validate new analytical methods
Design and execute method transfer protocols
Generate, write and revise SOPs, test methods, validation protocols and validation reports
Mentor chemists/analysts in the proper execution, including interpretation of validation parameters
Provide technical support to the analytical methods used for marketed products by QC lab and products in development phase
Achieve and maintain high standards with meticulous attention to detail
Conduct laboratory investigation activities
Troubleshoot different analytical instruments
Lead method development projects
Serve as technical lead for specific area of expertise
Assist Analytical Scientist III or Sr. Scientist in drafting publication or position papers
Interpret test results and compare with determined standards and limits.
Interpret and compare data to historical records and verifies trending
Take active role to ensure the laboratory is in compliance with cGMP and GDP
Assist in audit and compliance program to meet ISO17025 laboratory accreditation requirements (including statistical analysis of data)
Assist in drafting publication or position papers
Qualifications SKILLS AND BACKGROUND REQUIRED TO BE SUCCESSFUL:
Solid knowledge of cGMP and GDP
Well versed with various data acquisition/processing software and other laboratory controls
Highly proficient in most of lab instrumentation (i.e. FTIR, HPLC, ICP, GC, UV-Vis, LC-MS, GC-MS, ICP-MS, HPTLC) and test methods
Strong analytical and problem solving ability
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