POSITION SUMMARY
Responsible for performing routine testing, review documentation, and release into production raw materials, blends, encapsulated and finish goods. Additional duties will be to identify and resolve quality deviations in a timely manner in collaboration with the QC Supervisor.
- 2 years of college (Associates Degree) with an emphasis in a science-related field or minimum one-year work experience working in a Pharmaceutical, Dietary Supplement, Cosmetics, or Food manufacturing environment
- Knowledge of cGMP and GLP
- Strong written and verbal communication skills, to include the ability to communicate effectively with employees and management
- Excellent organizational skills, self-motivation, and to work in a fast-paced dynamic setting
- Must be willing to work overtime or on weekends, as the workload demands
- Perform routine testing of in-process raw materials, blends, encapsulated and finish good products in accordance with SOP’s
- Issue release label and forward release information to production and warehouse personnel
- Assist in the development of test methods for raw materials, in-process, and finished goods
- Ensure that lab cleanliness and safety standards are maintained
- Write, review, and revise QC SOPs or Guidelines
- Ensure proper documentation in laboratory notebooks and/or logbooks and double-check the work of other analysts
- Identify and resolve quality deviations in a timely manner in collaboration with the QC Supervisor
- Perform other duties and responsibilities, as assigned
WORK ENVIRONMENT
- Work location is in a laboratory setting. Other assignments may be in warehouse or on production floor.
- Duties are performed primarily in a smoke-free environment
PHYSICAL REQUIREMENTS
- Frequently required to stand, walk, bend, kneel, crouch, balance and reach.
- Regularly lift and/or move up to 50 lbs.