Job Description
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
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
#LI-GB1
US Benefits Statement: 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.
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
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
#LI-GB1
US Benefits Statement: 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.
💡 Quick Summary
Seeking a career-building opportunity? The Analytical Scientist I- post position is now open for candidates interested in the IT Engineer & Developer Jobs sector. This role in Los Angeles offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in IT Engineer & Developer Jobs is a plus.
