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Production Associate I – 1st Shift

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AtriCure
Published
April 19, 2022
Location
Mason, Ohio, ohio
Job Type

Description

AtriCure, Inc. provides innovative technologies for the treatment of Afib and related conditions. Afib affects more than 33 million people worldwide. Electrophysiologists and cardiothoracic surgeons around the globe use AtriCure technologies for the treatment of Afib and reduction of Afib related complications. AtriCure’s Isolator® Synergy™ Ablation System is the first medical device to receive FDA approval for the treatment of persistent Afib. AtriCure’s AtriClip® Left Atrial Appendage Exclusion System products are the most widely sold LAA management devices worldwide. AtriCure’s Hybrid AF™ Therapy is a minimally invasive procedure that provides a lasting solution for long-standing persistent Afib patients. AtriCure’s cryoICE cryoSPHERE® probe is cleared for temporary ablation of peripheral nerves to block pain, providing pain relief in cardiac and thoracic procedures. For more information, visit AtriCure.com or follow us on Twitter @AtriCure.

AtriCure is a fast-growing company that is looking to add Production Associates to help assemble our Medical Devices. Many Production employees have grown over time within the role to lead or supervise others or move to other areas within packaging, manufacturing, or quality.

 

POSITION HIGHLIGHTS:

  • 1st Shift position Monday- Friday 6:30 - 3:00 pm
  • Medical Device company that helps people with a heart condition called Afib.
  • Air-conditioned, cleanroom environment
  • Ranked top companies to work for in the Cincinnati area
  • Health benefits/401K start on day 1 of employment
  • PTO and Volunteer Time Off
  • Gym and Cafe on site; Free coffee daily
  • Lots of room to grow your career internally
  • Headquarters in Mason, OH (across from Kings Island)

POSITION SUMMARY:

Production Associate I is responsible for the manufacturing of components, the assembly and of finished products.  These individual manufactures product in compliance with production control documentation and he/she is under the direct supervision of the production supervisor.  This person is responsible for the quality of their work and meeting all Quality System requirements for the tasks assigned.

 

ESSENTIAL FUNCTIONS OF THE POSITION:

  • Assists with the movement of materials through the workstations and properly label all bins and trays
  • Identify gaps in individual employee training and/or deficiencies in production documentation
  • Performs company activities in addition to the above as assigned by production supervisor and/or Team leader, Level 2 or 3
  • Under guidance of team members performs in-process inspection per process specifications and inspection documentation
  • Assemble products per process specifications
  • Ensure products meet the current quality requirements
  • Raises issues or concerns with components, processes, documentation when needed
  • Responsible for operating equipment and processes per process specifications
  • Responsible for documenting time to appropriate manufacturing orders
  • Responsible for following process specifications and production rules
  • Helps with improving processes throughout the department or center of excellence

ADDITIONAL ESSENTIAL FUNCTIONS OF THE POSITION:

  • Regular and predictable work performance
  • Ability to work under fast-paced conditions
  • Ability to make decisions and use good judgment
  • Ability to prioritize various duties and multitask as required
  • Ability to successfully work with others
  • Additional duties as assigned

BASIC QUALIFICATIONS:

  • High School Diploma or demonstrated equivalent combination of education, training and experience.
  • Ability to handle and assemble small parts
  • Great attention to detail
  • Ability to work using microscopes and other magnifying aids
  • Good oral and communication skills
  • Professional interactions with customers and employees
  • Seeks out opportunities to learn new skills, and acquire information

PREFERRED QUALIFICATIONS:

  • Previous Medical Device industry experience
  • Assembly Experience and/ or experience in Manufacturing
  • Knowledge of cGMP and ISO standards

OTHER REQUIREMENTS:

  • Ability to regularly walk, sit, or stand as needed
  • Ability to occasionally bend and push/pull as needed
  • Ability to regularly lift up to 10 pounds, occasionally lift up to 25 pounds
  • Ability to use hands to grasp and manipulate small parts in a repetitive motion
  • On Demand overtime to meet production schedule may be required
  • Ability to pass pre-employment drug screen and background check

#LI-AM1

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