Chemist I

Herbalife • Winston-Salem, NC

8d • Onsite

About The Position

THE ROLE: The Chemist I will work onsite at our state of art Innovation and Manufacturing facility in Winston-Salem, NC. As an entry level chemist, will perform chemical and physical analysis of inner and outer nutritional products in the quality control lab using wet chemistry techniques and instrumental analyses. HOW YOU WOULD CONTRIBUTE : Performs laboratory testing (qualitative and quantitative chemical and physical analysis of raw materials, finished products and/or stability samples). Review/peer review of testing results in laboratory notebooks and in LIMs. Prepares standards and reagents; calibrates and operates sophisticated laboratory instrumentation such as HPLC, FTIR, UV- Visible spectrophotometer. Reviews product certificates of analysis for accuracy and conformance and maintain C of A files. Performs routine calibration and performance verification of lab equipment and instrumentation. Provides input on Standard Operating Procedures (SOPs), Test Methods and other relevant laboratory documents. Participate in investigations, address Out of Specifications (OOS), resolve deviations and implement CAPA with general supervision. Follow current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP). Documents data in lab notebook and follow basic cGMP guidelines. Interprets test results and compares with determined standards and limits. Interprets and compares data and records and trend verification under general supervision. Maintains a safe, clean and efficient laboratory. Chemist I is responsible to produce high quality laboratory data and empowered to stop an analysis that may produce poor quality results as required by ISO 17025. Other duties as assigned by management.

Requirements

• Ability to implement testing according to established methods.
• Demonstrates basic proficiency in lab instrumentation and multiple test methods.
• Ability to solve practical problems and carry out responsibilities under general supervision
• Ability to organize workload for effective implementation
• Strong customer and results orientation
• Ability to interact effectively at all levels with sensitivity to cultural diversity
• Ability to function as an effective team member
• Ability to adapt as the external environment and organization evolves
• 0 – 3 years previous experience in an analytical laboratory of qualitative or quantitative analyses
• Experience in wet chemical analysis and/or instrumental analysis utilizing FTIR, HPLC, GC and UV-Visible spectrophotometry
• Bachelor of Science in Chemistry, Biochemistry or related field or equivalent experience.

Nice To Haves

• Knowledge of LC/MS and GC/MS
• Previous cGMP regulation and compliance working knowledge/experience
• Nutraceutical or pharmaceutical laboratory working knowledge/experience
• Knowledge in ISO17025 Lab Management
• Master of Science in Chemistry or Biochemistry or related filed

Responsibilities

• Performs laboratory testing (qualitative and quantitative chemical and physical analysis of raw materials, finished products and/or stability samples).
• Review/peer review of testing results in laboratory notebooks and in LIMs.
• Prepares standards and reagents; calibrates and operates sophisticated laboratory instrumentation such as HPLC, FTIR, UV- Visible spectrophotometer.
• Reviews product certificates of analysis for accuracy and conformance and maintain C of A files.
• Performs routine calibration and performance verification of lab equipment and instrumentation.
• Provides input on Standard Operating Procedures (SOPs), Test Methods and other relevant laboratory documents.
• Participate in investigations, address Out of Specifications (OOS), resolve deviations and implement CAPA with general supervision.
• Follow current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP). Documents data in lab notebook and follow basic cGMP guidelines.
• Interprets test results and compares with determined standards and limits. Interprets and compares data and records and trend verification under general supervision.
• Maintains a safe, clean and efficient laboratory.
• Chemist I is responsible to produce high quality laboratory data and empowered to stop an analysis that may produce poor quality results as required by ISO 17025.
• Other duties as assigned by management.

Benefits

• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 5,001-10,000 employees