Chemist I

Herbalife•Winston-Salem, NC

About The Position

Chemist I, as an entry level chemist, will perform standard chemical and physical analysis of inner and outer nutritional products in the quality control lab using wet chemistry techniques and instrumental analyses.

Requirements

Ability to execute 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 various 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 knowledge
Nutraceutical or pharmaceutical laboratory work 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.
Comply with 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 historical records and trend verification under general supervision.
Maintains a safe, clean and efficient laboratory.
Chemist I is responsible to produce high quality laboratory data.
Chemist I is responsible for and empowered to stop an analysis that may produce poor quality results as required by ISO 17025.
Other duties as assigned by management.