Regulatory & Quality Associate Position Available In Pinellas, Florida

Regulatory & Quality Associate Global Good, Corp. Largo, FL Job Details Full-time $60,000 – $68,000 a year 18 hours ago Benefits Paid time off Qualifications CGMP Quality control within healthcare industry ISO standards Writing skills

FDA 21 CFR

Part 11 Attention to detail Manufacturing

ISO 13485

Editing Entry level FDA regulations Under 1 year Full Job Description Shape the Future of Medical Devices & Healthcare Innovation At Global Good Corp., we’re redefining the future of therapeutic and non-invasive technologies that improve lives. As a fast-growing medical device design and manufacturing company, we’re built on 35 years of engineering excellence and a proven track record of cutting-edge medical technology. We’re on an exciting journey to scale, innovate, and make a lasting impact in healthcare—and we’re looking for driven professionals to grow with us. If you’re passionate about innovation, thrive in a hands-on environment, and want to make a real impact, this is your opportunity to be part of something bigger. Key Responsibilities As our Regulatory & Quality Associate, you’ll play a critical role in supporting the documentation and compliance infrastructure that keeps our operations running smoothly and in compliance with

FDA 21 CFR

Part 820, ISO 13485, and other applicable standards and requirements.

Your responsibilities will include:

Supporting the ongoing management and evolution of our Quality Management System (QMS) documentation. Drafting and maintaining procedures, work instructions, forms, and records. Helping track and organize Design History Files (DHF), Device Master Records (DMR), and Device History Records (DHR). Assisting with internal audits, risk assessments, and version control. Collaborating with our engineering and production teams for editing/drafting documentation Learning about labeling requirements, document control, Corrective and Preventive Actions (CAPAs), and regulatory submissions. Contributing to process improvement efforts as we grow and scale. Qualifications Strong attention to detail and excellent writing/editing skills. An interest in medical devices, regulatory affairs, or quality systems. A degree in a relevant field (Engineering, Life Sciences, Health Sciences, etc.) or equivalent experience. The ability to work independently in a fast-paced environment. Eagerness to learn

FDA, ISO

13485, and other applicable standards (experience is a plus, but not required). Take the Next Step in Your Career! If you’re passionate about innovation, thrive in a dynamic environment, and want to make a real impact, we want to hear from you.

Job Type:

Full-time Pay:

$60,000.00 – $68,000.00 per year

Benefits:

Paid time off Ability to

Commute:

Largo, FL 33773 (Required) Ability to

Relocate:

Largo, FL 33773: Relocate before starting work (Required)

Work Location:

In person