Date Posted: 04/09/2025
Hiring Organization: Rose International
Position Number: 480978
Job Title: Production Operator
Job Location: Glasgow, KY, USA, 42141
Work Model: Onsite
Shift: Monday-Thursday 6a-430p; OT Friday 6a-4:30 PM Training - days 1 and 2 8:00 am-4:30 pm
Employment Type: Temporary
Estimated Duration (In months): 3
Min Hourly Rate ($): 17.00
Max Hourly Rate ($): 17.00
Must Have Skills/Attributes: Computer Literacy, Data Entry, FDA, Production Support
Job Description
Required Education:
• High School Diploma or GED
Required Qualifications/Skills/Experience:
• Review of completed batch records for compliance with cGMPs, validation, and standard operating procedure requirements. Reconcile labeling and product components and determine compliance with specifications.
• Assist in investigation of non-confirming results related to either reconciliation or production activities. 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 thermoforming equipment, perform on-line product inspections, off-line inspections, and leak testing in accordance with qualification requirements.
• Ability to perform at or above established quality and productivity standards on all lines. 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.
Production Operator Overview:
• 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 labeling and production equipment.
• Responsible for data entry and computer-generated labels.
• Maintains records and production area to comply with regulatory requirements, good manufacturing practices, and standard operating procedures.
• Performs reconciliation activities and determines compliance to specification, floats on all lines.
• Performs final production check of completed documents for completeness and accuracy.
Job Duties:
• Responsible for verification of materials and products as directed by procedures and or batch record requirements.
• Utilizes critical thinking and judgment to collaborate and inform the case management/concurrent review process, to facilitate appropriate healthcare outcomes for members by providing care coordination, support, and education for members through the use of care management/concurrent review tools and resources.
• Will assist with auth creation, appointment scheduling, and outreach to members, referral follow-up.
Industry: Healthcare
Estimated Start Date: 04/28/2025
Dress Code: Business Casual
**Only those lawfully authorized to work in the designated country associated with the position will be considered. **
**Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements. **
Benefits:
For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.
California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.
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