Vangard Quality Control Inspector

Company Name:
Performs inspections, checks testing and sampling procedures for printing and product production processes. 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.
Performance and or verification/documentation of pharmaceutical product, and packaging material incoming inspections for compliance with specifications and assembly (kitting) functions.
Performance/documentation of production line clearance inspections and printing inspections in line with operating schedules.
Assist with maintaining Quality Control Product Reference Standards.
Compliance with cGMPs and written procedures for all activities completed.
Responsible for maintaining competency for QC Inspector 1 responsibilities.
Ability to perform at or above established quality and productivity standards.
Perform additional duties as assigned by management.
Regular attendance is an essential function of the job.
Follow all applicable government regulations including HIPAA, FDA, OSHA, and EPA.
Display behavior which exemplifies employee code of conduct guidelines and Omnicare Core Values.
Other duties as assigned; Job duties may vary by location.
Minimum (Required): _(must be met in order to perform the job at the required level)_
High School Graduate, and + 2 years related work experience, or similar combination of education and experience.
Must have computer experience and proficient in Word and Excel.
Excellent oral and written communication skills.
Reliable with confidential information.
Ability to use expertise to solve problems.
Ability to prioritize.
Ability to work with very little supervision.
Proofreading Skills.
Preferred: _(if above and beyond the minimum required)_
Formal cGMP training or equivalent experience in regulated industry.
Associate Degree
Quality Control Inspection experience in a manufacturing environment.
Prior experience in a pharmaceutical environment.
Physical Demands: May sit, stand, stoop, bend and walk intermittently during the day. May sit or stand seven (7) to ten (10) hours per day. May be necessary to work extended hours as needed. Finger dexterity to operate office equipment required. May need to lift up to seventy-five (75) pounds on occasion. Visual acuity to see and read fine prints. Specific vision abilities required by this role include close vision, color vision and the ability to adjust focus. Must be able to hear normal voice sounds. The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this role.
Work Environment: Work in a climate-controlled, smoke-free internal environment.
Equal Opportunity Employer: Omnicare is fully committed to employing a diverse workforce. We recruit and retain talented individuals without regard to gender, race, age, marital status, disability, and veteran status or any other status protected by federal, state or local law. Omnicare is an Equal Employment Opportunity and Affirmative Action Employer.
Date: 2014-08-19
Country: US
State: KY
City: Glasgow
Postal Code: 42141
Category: Manufacturing
Job Type: Regular Full-Time

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