2nd Shift Technical Operator

Salary: USD
20.9 - USD
20.9 per hour

Technical Operator I

2 nd Shift Monday – Friday 2:00pm – 10:30pm, Pay: $20.90/hr

Receives a bump in pay upon conversion

Temp-to-Hire

Must be able to pass a background check and drug screen, prior to starting

The Technical Operator I utilizes an array of production equipment as well as manual assembly to manufacture and package cuvette products. The Technical Operator I is also responsible for an array of other manufacturing related tasks.

• Support daily production and packaging activities in accordance with Good Manufacturing Practices (GMP) and all related standard operating procedures (SOPs).
• Continually work to achieve assigned production goals; meet unscheduled peaks in workload as necessary to ensure timely release of product and to avoid back orders.
• Work with Team Leader and Supervisor to detail critical raw materials, in-process procedures, and specifications.
• Use computerized Materials Resource Planning (MRP) inventory system as required
• Maintain accurate records and documentation in accordance with Good Documentation Practices (GDP) and all related SOPs.
• Maintain safe working conditions at all times; adhere to all safety policies and procedures.
• Identify line issues and other production problems; promptly notify Team Leader or Supervisor of required corrective action.
• Operate production equipment as directed and in accordance with all SOPs.
• Perform in-process quality checks on sub-assemblies and finish products.
• Support all efforts and procedures to maintain optimal manufacturing conditions.
• Ensure production areas are continually kept clean.
• As directed, provide support for process and equipment validation.
• Maintain daily product logbooks as directed.
• Ensure and maintain compliance with the Company’s quality system requirements through training and adherence to policies, procedures and processes.
• Other duties as assigned.

• Warehouse
• Engineering

• High school diploma or equivalent.
• At least two (2) years previous assembly/packaging experience; previous experience in a regulated medical device manufacturing or pharmaceutical environment strongly preferred.

• Previous experience with, or ability to, quickly comprehend manufacturing processes.
• Familiarity with GDP, GMP, Good Laboratory Practices (GLP), FDA, and ISO.
• Working knowledge of Microsoft Office and large Enterprise Resources Planning (ERP) system preferred.
• Good written and verbal communication.
• Ability to work as part of a team.

CV / Resume:
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