Flow Technician

Work Schedule

Environmental Conditions

Job Description

As part of the Thermo Fisher Scientific team youll 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 worlds 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.


A Day in the Life: 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.




Education:
High school diploma or equivalent required. (technical or manufacturing certification preferred)


Experience:
Required: Minimum of 4 years of work experience in a manufacturing operations production or lab setting or related field
Preferred: 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.


Knowledge Skills Abilities: 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


Physical Requirements / Work Environment
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What We Offer:

Compensation
Competitive Pay
Performance Related Bonus where eligible
Annual merit performance-based increase

Excellent Benefits
Medical benefits
Paid Time Off/Annual Leave
Employee Referral Bonus
Career Advancement Opportunities