Entry-Level Medical Device Operations Associate

Confluent Medical; Chattanooga, Northern (TN, KY); Hybrid; USD 34,000 - 42,000; Full time

Job summary

Confluent Medical Technologies in Chattanooga, TN, is seeking an Operations Associate I to contribute to balloon catheter manufacturing.

You will read and follow documentation, maintain GMP standards, and work with team members to ensure quality results.

Responsibilities include processing materials, recording data, and adapting to a fast-paced environment while upholding safety and quality practices.

Qualifications

• High school diploma or equivalent, and 0-2 years related experience and/or training, or an equivalent combination of education and experience.
• Ability to read, write, understand, and communicate in English to comprehend simple instructions and short correspondence.
• Ability to add, subtract, multiply, and divide
• Knowledge of good manufacturing practices (GMP)
• Strong attention to detail, professional attitude, team player

Responsibilities

• Manufacture medical device balloons per specifications
• Read, follow, and accurately complete all provided documentation (product drawings, work procedures, process logs, etc.)
• Have some computer proficiency with a willingness to learn computer systems required to perform job responsibilities
• Be able to prioritize effectively and manage multiple process responsibilities
• Demonstrate personal initiative and the ability to effectively execute tasks independently
• Follow good manufacturing practices (GMP): line clearance, work instructions, documentation, etc.
• Be willing to work in a fast-paced manufacturing environment and have ability to modify work shift as needed by business conditions
• Communicate problems to supervisor or lead
• Seek clarity from supervisor or lead when needed
• Perform other duties as required

Education

High school diploma or equivalent

Job description

Confluent Medical Technologies in Chattanooga, TN, is seeking an Operations Associate I to contribute to balloon catheter manufacturing.

You will read and follow documentation, maintain GMP standards, and work with team members to ensure quality results.

Responsibilities include processing materials, recording data, and adapting to a fast-paced environment while upholding safety and quality practices.