Coordinator, Vanguard Quality Control Inspector (Omnicare)

At CVS Health, we're building a world of health around every consumer and surrounding ourselves with dedicated colleagues who are passionate about transforming health care.As the nation's leading health solutions company, we reach millions of Americans through our local presence, digital channels and more than 300,000 purpose-driven colleagues - caring for people where, when and how they choose in a way that is uniquely more connected, more convenient and more compassionate. And we do it all with heart, each and every day.Position Summary

The Coordinator, Vanguard Quality Control Inspector (Omnicare) performs inspections, and checks testing and sampling procedures for printing and product production processes. This person carries out production line clearance inspections and sampling and testing of incoming components and raw materials to ensure that company specifications are met. Assembles and or verifies product & component assembly (kits). Performs batch record reviews to assure compliance to procedures, specifications, and validated parameters. Applies approval or rejection labels to materials once data is evaluated. A substantial portion of the duties require physical tasks performed in the warehouse/production areas.Key Responsibilities:

• Performance and or verification/documentation of pharmaceutical product, and packaging material incoming inspections for compliance with specifications and assembly (kitting) functions.
• Verify performance/documentation of production line clearance.
• Printed label inspections in line with operating schedules.
• Assist with maintaining Quality Control Product Reference Standards.
• Compliance with cGMPs ( current Good Manufacturing Practices ) and written procedures for all activities completed.
• Drive tow motor to retrieve product from locations; daily use of pallet jacks to move heavy loads within warehouse areas.
• Ability to perform at or above established quality and productivity standards.
• Perform additional duties as assigned by management.

• At least 1 year of experience in customer service.
• Proficiency with desktop software applications such as Outlook, Word, PowerPoint, Teams, and Salesforce.
• Ability to be fully on-site in the Glasgow, KY office.
• Ability to work either five 8-hour shifts (Mon-Thurs) or four 10-hour shifts, in between 6a-4:30p CT.
• Demonstrated ability to distinguish color visually, and willingness to take and pass a vision assessment.

• Extraordinary attention to detail, including comparisons of numbers and letters, with both paper-based and also computer screen records and documents. Excellent oral and written communication skills.
• Ability to focus carefully on quality inspections or accurate document review tasks for extended periods.
• Takes pride in maintaining high quality standards in a challenging regulated manufacturing environment.
• Reliable with confidential information.
• Ability to use expertise to solve problems.
• Ability to prioritize.
• Ability to work with very little supervision.
• Proof Reading Skills. Formal cGMP training or equivalent experience in regulated industry.
  Quality Control Inspection experience in a manufacturing environment.
• Prior experience in a pharmaceutical environment.

• Affordable medical plan options, a 401(k) plan (including matching company contributions), and an employee stock purchase plan.
• No-cost programs for all colleagues including wellness screenings, tobacco cessation and weight management programs, confidential counseling and financial coaching.
• Benefit solutions that address the different needs and preferences of our colleagues including paid time off, flexible work schedules, family leave, dependent care resources, colleague assistance programs, tuition assistance, retiree medical access and many other benefits depending on eligibility.