**New Hires eligible for $2,000 Sign-On Bonus!** 2nd Shift: 2:00pm – 10:30 pm (Mon-Fri) (Shift Differential = 6% of hourly wage) *Spanish/English bilingual is a plus, but not required Position Overview The QA Associate I, Process Quality Inspector provides quality assurance support and leadership to the Production Department. The QA Associate I, Process Quality Inspector provides a strong floor presence and works directly with production supervision and operators to maintain quality of manufacturing operations. Essential Job Functions • Works with Production personnel to ensure compliance of CPI practices, policies, and procedures. A significant focus on batch record and process compliance is expected. Performs routine review of in process production documents during processing to ensure accuracy and completeness. • Performs routine inspections/audits on personnel, procedures, equipment, and products. • Provides leadership to Production personnel on quality issues. • Initiates deviations and documents initial investigations. May contribute to assessment of deviations under the direction of the supervisor. • Contributes to quality investigations. Serves as lead investigator when assigned by the supervisor. • Initiates, maintains, and dispositions non-conformances. • Assists in training of Production personnel in company practices, policies, and procedures. • Assists in the movement of controlled substances into/out of the controlled substance storage and processing areas. • Performs sampling activities when assigned by the supervisor. • Reviews unit logbooks and/or environmental monitoring data as assigned. • Follows all CPI cGMP practices, policies, and procedures. • Follows all CPI safety practices, policies, and procedures. • Employees at CPI work with and/or are familiar with the GMP requirements for Food, Dietary Supplements, Pharmaceuticals, or other elements of each. • Depending on the position, the employee will be aware of Halal and/or Kosher requirements. • Other duties as assigned. Education/Skills/Knowledge Required • High School diploma or equivalent. • 2-3 years of industry quality or cGMP manufacturing experience required. Formal quality training may be substituted in place of experience. • Knowledge of current Good Manufacturing Practices (cGMPs) preferred. • Knowledge of a variety of cGMP manufacturing practices preferred (including fluid bed coating/granulation, capsule filling, milling, tableting) • Strong attention to detail and problem-solving skills required. • Ability to read, write (legibly), and speak the English language at a level necessary for efficient job performance. • Ability to establish and maintain effective working relationships with team members, co-workers, and/or clients. • Ability to stand for extended periods of time and lift objects weighing up to 55 lbs.