Coordinator – Vanguard Quality Control Inspector – Omnicare
| Company | CVS Health |
|---|---|
| Location | Barren County, KY, USA |
| Salary | $17 – $25.65 |
| Type | Full-Time |
| Degrees | |
| Experience Level | Entry Level/New Grad, Junior |
Requirements
- 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.
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.
Preferred Qualifications
- 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.