Production Operator I – Part-Time

Production Operator I – Part-Time

Requirements

• At least 6 months of experience in customer service.
• Ability to be fully on-site in the Glasgow, KY office.
• Ability to work two days per week (between Monday-Thursday) from 6:00am-4:30pm CT.
• Demonstrated ability 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 have a willingness to take and pass a vision assessment.
• Demonstrated finger dexterity for repetitive operative use of facility equipment.

Responsibilities

• Responsible for verification of materials and products as directed by procedures and/or batch record requirements.
• Responsible for labeling, inspecting, and production of final container products with manual and/or automated systems.
• Also responsible for set-up, changeover, and operation of bottle opening equipment.
• Maintains records and production area to comply with regulatory requirements, good manufacturing practices, and standard operating procedures.
• May perform initial check of completed documents for completeness and accuracy.
• Bottle opening equipment set-up, cleaning, and operation in accordance with cGMPs (*current Good Manufacturing Practices*) and internal standard operating procedures.
• Inspection of bulk drug and determination of conformance to specifications identify shortages.
• Maintenance of logs, batch records, and all applicable documentation in accordance with cGMP specifications and internal standard operating procedures.
• Maintain qualification to clean and verify bottle-opening equipment and to perform off-line inspections in accordance with qualification requirements.
• Ability to perform at or above established quality and productivity standards.
• Responsible for maintaining competency for Production Operator 1 responsibilities.
• Regular attendance is an essential function of the job.
• Follow all applicable government regulations including HIPAA (*Health Insurance Portability and Accountability Act*), FDA (*Food and Drug Administration*), OSHA (*Occupational Safety and Health Administration*), and EPA (*Environmental Protection Agency*).
• Display behavior which exemplifies employee code of conduct guidelines and Omnicare Core Values.
• Perform additional duties as assigned by management.
• May be necessary to work extended hours as needed.

Preferred Qualifications

• Prior experience in a manufacturing or pharmaceutical environment.
• Assembly experience.
• Light mechanical industry experience.
• Basic awareness of problem solving and decision-making skills.
• Attention to detail.