Flow Technician

Thermo Fisher Scientific•Marietta, OH

1d•Onsite

About The Position

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Location/Division Specific Information: (No more than 2-3 sentences) The Marietta Manufacturing site is a part of the Laboratory PEquipment Division. Our laboratory equipment products are used primarily by pharmaceutical companies for drug discovery and development and by biotechnology companies and universities for life science research to advance the prevention and cure of diseases and enhance quality of life. Our offering consists of equipment, accessories, and services for sample preparation, storage and protection, and analysis. How Will You Make an Impact? The Flow Technician supports efficient, compliant assembly of medical device equipment across non-classified, Class I, and Class II product lines. The role ensures smooth production flow, rapid resolution of the line issues, and a strict adherence to applicable quality system, regulatory, and safety requirements.

Requirements

High school diploma or equivalent required. (technical or manufacturing certification preferred)
Minimum of 4 years of work experience in a manufacturing, operations, production or lab setting or related field
Strong attention to detail and ability to follow documented procedures.
Basic mechanical aptitude and problem-solving skills.
Effective communication skills and ability to work cross-functionally
Able to lift 40 lbs. without assistance
Adherence to all Good Manufacturing Practices (GMP) Safety Standards
Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Standing for full shift

Nice To Haves

Experience in a cGMP environment
1-3 years of experience in manufacturing; experience in regulated environments preferred
Working knowledge of GMP and quality system requirements; familiarity with FDA 21 CFR part 820 and ISP 13485 preferred.

Responsibilities

Monitor and maintain production flow across medical device assembly lines to meet output, quality, and compliance targets.
Identify and resolve bottlenecks, material shortages, and minor equipment issues in real time.
Coordinate with Production, Quality, Engineering, Maintenance, and Material teams to support uninterrupted operations.