More jobs:
Project Manager, Medical Device Industry
Job in
Buford, Gwinnett County, Georgia, 30518, USA
Listed on 2026-03-03
Listing for:
Theragenics
Full Time
position Listed on 2026-03-03
Job specializations:
-
Healthcare
Medical Device Industry -
Engineering
Medical Device Industry
Job Description & How to Apply Below
Company Overview
At Theragenics, we're committed to transforming healthcare and enhancing patient outcomes through innovation. As a global leader in medical device development, we specialize in minimally invasive treatments for cancer, vascular procedures, and surgical applications. Headquartered in Atlanta, Georgia, with facilities in Costa Rica, Texas, and Massachusetts, we proudly operate Arrotek, a visionary medical device design consultancy in the U.S. and Ireland, dedicated to pioneering solutions that enhance lives.
As the Project Manager, you will manage high-impact, strategic projects that are critical to the company's future global business operations. You must have in depth knowledge in engineering, production, quality, regulatory and Medical devices product cycle, and previously working in Medical devices or Pharmaceutical company for minimum 8 years.
Your project leadership is crucial to our continued growth. In this role, you will have the freedom to innovate while collaborating with teams across Ireland, Texas, Boston, Atlanta, and Costa Rica. You will leverage your experience in the Medical Device lifecycle, from development and validation to commercialization.
This is a high-visibility position, and you will be communicating directly with senior leadership, demonstrating your impact through clear updates on progress, milestones, and key results. If you are a proactive project leader ready to make a difference in a dynamic, fast-paced environment, this role is your opportunity to stand out.
The Project Manager role offers independence and responsibility. You will contribute to the company's strategic direction from your first day by:
- Diving into our business operations to quickly understand how we work, what drives our success, and who our key stakeholders are.
- Taking on and guiding a $20 million production SKU transfer to our Costa Rica manufacturing facility.
- Collaborating with Engineering, Operations, Quality, Sales and Regulatory teams to ensure all projects comply with medical device industry standards and regulations.
- Leading cross-functional teams through the product and process development stages while ensuring compliance with medical device industry standards and regulations.
- Developing project plans, schedules, risk registers, budgets, and resource allocation for designated projects.
- Managing project execution, meetings, documenting meeting minutes and pivotal decisions, and diligently tracking action items.
- Bachelor's Degree in Engineering or other Scientific discipline. Applicants demonstrating relevant professional experience may qualify regardless of educational background.
- Minimum 3 years work experience as a lead engineer in Operation, engineering, or quality role.
- Full understanding of Medical Device Lifecycle. In-depth knowledge of medical device or Pharmaceutical R&D, product development, Validation, and clinical/regulatory procedures.
- Advanced use of PM software and knowledge of business analysis tools such as Power BI.
- PMP certification or other PM certification is not a must, but an advantage.
- Career Growth: High-visibility role with opportunities to influence strategic direction.
- Innovative Projects: Work on complex, global initiatives that drive healthcare innovation.
- Collaborative Culture: Partner with diverse teams across multiple countries.
- Competitive Benefits: Comprehensive health, wellness, and financial packages.
- Purpose-Driven Work: Make a real impact on patient care worldwide.
"We don't just ship inventory; we deliver care."
"Healthcare that is both high-tech and human, with a global reach but a personal impact."
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