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QA Associate I, Process Quality Inspector

Coating Place, Inc.
Verona, WI Full Time
POSTED ON 1/29/2025
AVAILABLE BEFORE 3/29/2025

**$2,000 Sign-On Bonus!** 

2nd Shift: 2:00pm – 10:30 pm (Mon-Fri) (Shift Differential = 6% of hourly wage) 


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.

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