Vangard Quality Control Supervisor

Company Name:
Responsible for coordinating, monitoring, and reviewing the work schedules, training and performance of the QC inspectors. The QC Supervisor ensures production needs are fulfilled on time to meet customer needs by effectively managing the QC performance of Incoming Inspection, Batch Record Review, Product Disposition, Production Support, Standards, Printing Operations, Investigations, and retained sample review. Works proactively with other QC and Production team leaders to assure that internal and external customer needs are met through effective integration of the activities of multiple lines and shift schedules.
Performance/documentation of incoming material inspections, disposition, and job kitting functions.
In-process, batch record and finished goods inspections, and product dispositions.
Performance/documentation of retained sample reviews & purging, and returned product inspections.
Approval and maintenance of product standards.
Coordination of investigations and preparation of reports.
Schedule/coordinate work of shift/technicians to meet production schedules.
Ensure staff is effectively trained to follow procedures, schedules, and cGMPs.
Compliance with cGMPs and written procedures for all activities completed.
Responsible for maintaining competency for Quality Control Supervisor responsibilities.
Ability to perform at or above established quality and productivity standards.
Responsible for maintaining competency for QC Inspector 1-3 responsibilities.
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) Qualifications: _(must be met in order to perform the job at the required level)_
B.S. Degree or Associates Degree with 5 years experience in Quality Assurance or Quality Control +3 years supervisory or similar combination of education and experience.
Proficient in MS Office applications.
Excellent oral and written communications skills.
Preferred Qualifications: _(if above and beyond the minimum required)_
+5 years supervisory in Pharmaceutical Quality Control/Regulatory/Quality
Formal cGMP training and equivalent experience in regulated industry
Quality Control/Statistical Process Control Experience
Root cause analysis training and experience
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: 2014-08-20
Country: US
State: KY
City: Glasgow
Postal Code: 42141
Category: Manufacturing
Job Type: Regular Full-Time

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