Analytical Scientist I

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

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
• Strong trouble shooting ability for analytical instruments
• Sound theoretical and practical knowledge of chromatography and spectrometry
• Good verbal and written communication skills (technical writing and presentation)
• Ability to communicate and work effectively in a team-based environment
• Good organizational skills
• Ability to manage and handle multiple projects simultaneously

Experience:

• 7 years of experience in analytical method development and validation field
• 3+ years of experience working in a cGMP environment
• Extensive technical experience in analysis of dietary supplements, food and personal care products

Education:

• Bachelor of Science in Chemistry, Biochemistry or related scientific fields

PREFERRED QUALIFICATIONS: 

• Solid knowledge in method development DOE
• Proficient in NMR
• Solid knowledge in ISO17025 Lab Management
• Master of Science in Chemistry, Biochemistry or related scientific fields

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Herbalife offers a variety of benefits to eligible employees in the U.S. (limited to the 50 States and the District of Columbia), which includes Group Health Programs, other Voluntary Benefit Programs, and Paid Time Off. Group Health Programs include Medical, Dental, Vision, Health Savings Account (HSA), Flexible Spending Accounts (FSA), Basic Life/AD&D Short-Term and Long-Term Disability, and an Employee Assistance Program (EAP). Other Voluntary Benefit Programs include a 401(k) plan, Wellness Incentive Program, Employee Stock Purchase Plan (ESPP), Supplemental Life/Critical Illness/Hospitalization/Accident Insurance, and Pet Insurance. Paid time off includes Company-observed U.S. Holidays, Floating Holidays, Vacation, Sick Time, a Volunteer Program, Paid Maternity and Paternity Leave, Bereavement Leave, Personal Leave and time off for voting.