General Assembler

Millenniumsoft•Mannford, OK

77d•Onsite

About The Position

Performs any combination of tasks involved in the fabrication, manufacture, assembly, testing and packaging of medical devices as well as setting up, operating, performing maintenance on and troubleshooting equipment. May conduct quality inspections on processing line in accordance with quality specifications. Works within clearly defined SOPs and / or scientific methods and adheres to quality guidelines. Performs routine assembly production functions including utility operations, and basic inspecting under direct supervision with the help of tools and equipment while working safely and efficiently. Applies basic knowledge and techniques with the help of job aids, standard operating procedures, and product specifications to complete routine task and process requirements. Develops skills in basic tasks, technique and procedures within multiple areas and processes.

Requirements

High school diploma or equivalent
Zero (0) to one (1) year of manufacturing assembly experience
Effective communication skills at a level co-workers and Team Lead/Supervisor can understand
Ability to read, write, interpret and comprehend specifications written in English and perform basic math calculations
Ability to use basic tools of measurement, such as microscopes
Must be able to work flexible and/or extended hours and report to work on a regular, punctual basis
Has good attention to detail
Ability to get along with people and be able to work in a team environment
Willingness to rotate into different tasks and responsibilities
While performing the duties of this job, the employee is regularly required to stand, walk, and sit for extended periods of time
Occasionally the employee may be required to lift or move at least 50 pounds
Ability to read, write, interpret, and comprehend specifications written in English and perform basic math calculations
Must be able to use basic measuring equipment and tools
Maintains accurate records and logs in accordance with GMPs (Good Manufacturing Practices) and ISO9000 (International Organization for Standardization) and FDA (Food and Drug Administration)
Effectively works in a team setting, supporting team goals and objectives
Ability to get along with people and be able to work in a team environment
Effective communication skills at a level co-workers, Lead and Supervisor can understand
Must be able to work flexible and/or extended hours and report to work on a regular, punctual basis
Must be able to maintain neat, legible, accurate, and complete documentation, records, and logs
Must be able to focus continuous attention to work processes
Must be willing to work overtime if necessary
Must be willing to help in all areas of production
Must be able to Stand/sit for long periods of time
No manufacturing experience required
While performing the duties of this job, the employee is regularly required to stand, walk, sit and use hands to manipulate, handle or feel objects, tools, controls and equipment
Occasional reaching, bending ,stooping or crouching is required

Responsibilities

Performs any combination of tasks involved in the fabrication, manufacture, assembly, testing and packaging of medical devices
Setting up, operating, performing maintenance on and troubleshooting equipment
Conduct quality inspections on processing line in accordance with quality specifications
Works within clearly defined SOPs and / or scientific methods and adheres to quality guidelines
Performs routine assembly production functions including utility operations, and basic inspecting under direct supervision with the help of tools and equipment while working safely and efficiently
Applies basic knowledge and techniques with the help of job aids, standard operating procedures, and product specifications to complete routine task and process requirements
Develops skills in basic tasks, technique and procedures within multiple areas and processes
Performs light assembly by following released procedures using tools and equipment
Performs changeovers, and setup and completes Required Device History Record (DHR) documentation
Must be able to read and understand: assembly instructions, work orders, Bills of Materials, Standard Operation Procedures, and all other documentation used to control our products and processes
Expected to provide feedback on production and methods, product design issues, continuously strives to improve product quality and operational efficiency
Communication with co- workers, Lead and Supervisor
Maintains Hour by hour production paperwork, boards or graphs
Keep work area clean organized and safe