Quality Control/Chemistry Supervisor

Herbalife•Winston-Salem, NC

3d•Onsite

About The Position

The 1st shift Chemistry Supervisor will be part of the Quality Control group and will work onsite at our state of art Innovation and Manufacturing facility in Winston-Salem, NC. Will be responsible for monitoring and guiding day to day testing activities in the Quality Control laboratory. Will work with and train Analysts and Technicians to conduct testing on raw materials and final products, reviews test results for accuracy and assures the tests adhere to internal SOPs and guidelines. The Supervisor will also communicate to other departments outside of the QC lab to report test results for release, screening, and stability. This position will maintain the bench work in compliance with cGMP & ISO 17025 requirements including Herbalife protocols, policies and procedures.

Requirements

5 years’ experience performing analytical chemistry testing in a laboratory environment
Prior experience leading projects or other initiatives.
Laboratory Compliance experience
Bachelor's degree with a major in a Chemistry or relevant scientific discipline
GMP Course Training
Regulatory training
Ability to work with all levels in organization and to persuade/negotiate with cross-functional team
Excellent communication skills, writing and computer skills are essential (working knowledge of Microsoft Office---word, Excel and power point)
Knowledge in relevant fields of analytical techniques
Demonstrated analytical and organizational skills
Attention to detail
Demonstrated/documented ability to work in a team
Ability to multi-task and prioritize
Ability to repair instruments/troubleshoot
Ability to optimally present information in one-on-one or in group situations

Nice To Haves

Laboratory Supervisory Experience
Communication and presentation skills
Motivational skills
Pharmaceutical or Nutraceutical GMP experience
Materials testing experience
Laboratory testing experience
Microsoft Office Proficiency Course
Trouble shooting experience

Responsibilities

Manage laboratory compliance and adherence to SOPs and test methods.
Provide reports to management pertaining to laboratory activities.
Handle OOS investigations.
Provide training on cGMP compliance in laboratory operations.
Support other Supervisors in interacting with regulatory authorities on laboratory compliance.
Participate in auditing and regulatory inspections.
Evaluate Analysts on laboratory practices.
Provide troubleshooting guidance and potential solutions for laboratory problems.
Ensure scheduled tasks are completed by Analysts.
Responsible for producing high quality laboratory data.
Responsible for and empowered to stop an analysis that may produce poor quality results as required by ISO 17025.
Perform other duties as assigned.