Interacts cooperatively with co-workers and receives direction well from managers * Displays ... Able to discuss status of projects and needs and appropriate turnaround time. Minimum Knowledge ...
New
Interacts cooperatively with co-workers and receives direction well from managers * Displays ... Able to discuss status of projects and needs and appropriate turnaround time. Minimum Knowledge ...
New
Interacts cooperatively with co-workers and receives direction well from managers * Displays ... Able to discuss status of projects and needs and appropriate turnaround time. Minimum Knowledge ...
New
Interacts cooperatively with co-workers and receives direction well from managers * Displays ... Able to discuss status of projects and needs and appropriate turnaround time. Qualifications ...
Interacts cooperatively with co-workers and receives direction well from managers * Displays ... Able to discuss status of projects and needs and appropriate turnaround time. Qualifications ...
Alpharetta, GA · On-site
$150 - $210/hr
Manage team by financial results that include sales growth, margins, pipeline size, conversion rate, costs, and use of the Salesforce tool. Provide clear goals and objectives for the team * Ensure a ...
Alpharetta, GA · On-site
$150 - $210/hr
Manage team by financial results that include sales growth, margins, pipeline size, conversion rate, costs, and use of the Salesforce tool. Provide clear goals and objectives for the team * Ensure a ...
Covington, GA · On-site
$150K - $165K/yr
Act as the primary regulatory contact for assigned projects, communicating directly with regulatory ... Minimum of 8-10 years of experience in Regulatory Affairs within the medical device industry, with ...
Covington, GA · On-site
$150K - $165K/yr
Act as the primary regulatory contact for assigned projects, communicating directly with regulatory ... Minimum of 8-10 years of experience in Regulatory Affairs within the medical device industry, with ...
Zebulon, GA · On-site
$110 - $160/hr
... medical devices within combination products. Responsibilities include risk management ... You will have opportunities to lead projects, broaden technical skills, and influence quality ...
Zebulon, GA · On-site
$110 - $160/hr
... medical devices within combination products. Responsibilities include risk management ... You will have opportunities to lead projects, broaden technical skills, and influence quality ...
Digital, artifact-driven evidence management * Agile and DevOps-aligned workflows * AI-enabled ... Medical device industry (preferred), or regulated software development * Software development ...
Digital, artifact-driven evidence management * Agile and DevOps-aligned workflows * AI-enabled ... Medical device industry (preferred), or regulated software development * Software development ...
... and project management. You will assess cutting edge technology that will make a difference in ... Manage certification activities for a portfolio of medical device manufacturers, including ...
... and project management. You will assess cutting edge technology that will make a difference in ... Manage certification activities for a portfolio of medical device manufacturers, including ...
Solid understanding of FDA regulations (21 CFR Part 820), ISO 13485, and medical device regulatory requirements. * Strong organizational and project management skills with the ability to manage ...
Quick apply
Solid understanding of FDA regulations (21 CFR Part 820), ISO 13485, and medical device regulatory requirements. * Strong organizational and project management skills with the ability to manage ...
Solid understanding of FDA regulations (21 CFR Part 820), ISO 13485, and medical device regulatory requirements. * Strong organizational and project management skills with the ability to manage ...
Solid understanding of FDA regulations (21 CFR Part 820), ISO 13485, and medical device regulatory requirements. * Strong organizational and project management skills with the ability to manage ...
... and project management. You will assess cutting edge technology that will make a difference in ... Manage certification activities for a portfolio of medical device manufacturers, including ...
... and project management. You will assess cutting edge technology that will make a difference in ... Manage certification activities for a portfolio of medical device manufacturers, including ...
Atlanta, GA · On-site
$90 - $120/hr
Solid understanding of FDA regulations (21 CFR Part 820), ISO 13485, and medical device regulatory requirements. * Strong organizational and project management skills with the ability to manage ...
Atlanta, GA · On-site
$90 - $120/hr
Solid understanding of FDA regulations (21 CFR Part 820), ISO 13485, and medical device regulatory requirements. * Strong organizational and project management skills with the ability to manage ...
Solid understanding of FDA regulations (21 CFR Part 820), ISO 13485, and medical device regulatory requirements. * Strong organizational and project management skills with the ability to manage ...
Solid understanding of FDA regulations (21 CFR Part 820), ISO 13485, and medical device regulatory requirements. * Strong organizational and project management skills with the ability to manage ...
In-depth knowledge of FDA regulations, 21 CFR Part 820, ISO 13485, and other applicable medical device regulations. * Strong leadership and project management skills, with the ability to manage ...
Quick apply
In-depth knowledge of FDA regulations, 21 CFR Part 820, ISO 13485, and other applicable medical device regulations. * Strong leadership and project management skills, with the ability to manage ...
In-depth knowledge of FDA regulations, 21 CFR Part 820, ISO 13485, and other applicable medical device regulations. * Strong leadership and project management skills, with the ability to manage ...
In-depth knowledge of FDA regulations, 21 CFR Part 820, ISO 13485, and other applicable medical device regulations. * Strong leadership and project management skills, with the ability to manage ...
Alpharetta, GA · On-site
Solid knowledge of medical device regulatory frameworks and quality standards . * Highly analytical with the ability to translate market data into actionable strategies. * Strong project management ...
Alpharetta, GA · On-site
Solid knowledge of medical device regulatory frameworks and quality standards . * Highly analytical with the ability to translate market data into actionable strategies. * Strong project management ...
In-depth knowledge of FDA regulations, 21 CFR Part 820, ISO 13485, and other applicable medical device regulations. * Strong leadership and project management skills, with the ability to manage ...
In-depth knowledge of FDA regulations, 21 CFR Part 820, ISO 13485, and other applicable medical device regulations. * Strong leadership and project management skills, with the ability to manage ...
Alpharetta, GA · On-site
Solid knowledge of medical device regulatory frameworks and quality standards . * Highly analytical with the ability to translate market data into actionable strategies. * Strong project management ...
Alpharetta, GA · On-site
Solid knowledge of medical device regulatory frameworks and quality standards . * Highly analytical with the ability to translate market data into actionable strategies. * Strong project management ...
This opportunity is ideal for someone with healthcare, medical device, DME, pharmaceutical, or ... The Territory Account Manager - Continuous Glucose Monitoring (CGM) is responsible for developing ...
This opportunity is ideal for someone with healthcare, medical device, DME, pharmaceutical, or ... The Territory Account Manager - Continuous Glucose Monitoring (CGM) is responsible for developing ...
This opportunity is ideal for someone with healthcare, medical device, DME, pharmaceutical, or ... The Territory Account Manager - Continuous Glucose Monitoring (CGM) is responsible for developing ...
Quick apply
This opportunity is ideal for someone with healthcare, medical device, DME, pharmaceutical, or ... The Territory Account Manager - Continuous Glucose Monitoring (CGM) is responsible for developing ...
Alpharetta, GA · On-site
$110 - $160/hr
Solid knowledge of medical device regulatory frameworks and quality standards. * Highly analytical with the ability to translate market data into actionable strategies. * Strong project management ...
Alpharetta, GA · On-site
$110 - $160/hr
Solid knowledge of medical device regulatory frameworks and quality standards. * Highly analytical with the ability to translate market data into actionable strategies. * Strong project management ...
$32.5K - $42K
2% of jobs
$42K - $51.5K
6% of jobs
$51.5K - $60.9K
10% of jobs
$66.1K is the 25th percentile. Wages below this are outliers.
$60.9K - $70.4K
13% of jobs
$70.4K - $79.9K
14% of jobs
The median wage is $83.3K / yr.
$79.9K - $89.4K
15% of jobs
$89.4K - $98.9K
13% of jobs
$101K is the 75th percentile. Wages above this are outliers.
$98.9K - $108.4K
12% of jobs
$108.4K - $117.8K
7% of jobs
$117.8K - $127.3K
5% of jobs
$127.3K - $136.8K
3% of jobs
$32.5K
$86.7K
$136.8K
A Medical Device Project Manager oversees the planning, development, and launch of medical devices, ensuring compliance with regulatory standards. They coordinate cross-functional teams, manage timelines, budgets, and risks, and facilitate communication between stakeholders. Their role involves working closely with engineering, regulatory, quality, and marketing teams to bring safe and effective medical devices to market.
As a Medical Device Project Manager, your daily duties typically include coordinating the activities of cross-functional teams—such as engineering, quality assurance, regulatory affairs, and marketing—to ensure project milestones are met. You'll oversee timelines, budgets, and documentation, while also addressing risks, facilitating communication, and managing stakeholder expectations. Regular tasks might involve leading project meetings, updating project trackers, monitoring regulatory compliance, and troubleshooting challenges that arise throughout the product development lifecycle. Successful project managers balance strategic planning with hands-on problem solving to keep complex medical device projects moving smoothly toward launch.
To thrive as a Medical Device Project Manager, you need a strong knowledge of medical device development, regulatory compliance, and project management, often supported by a background in engineering or life sciences and certifications like PMP or Six Sigma. Familiarity with tools such as Microsoft Project, quality management systems (QMS), and regulatory submission platforms (such as FDA eSubmitter) is highly valuable. Excellent leadership, problem-solving skills, and effective communication are essential for coordinating cross-functional teams and navigating complex project demands. These skills are crucial for delivering compliant, high-quality medical devices on time and within budget while ensuring collaboration across technical and clinical stakeholders.
For Medical Device Project Manager jobs in Georgia, the most frequently searched job titles are:
The top searched job categories for Medical Device Project Manager jobs in Georgia are:
Cities in Georgia with the most Medical Device Project Manager job openings:

Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 2 days ago
New
8.7
Based on 27 frontline employees who took The Breakroom Quiz
Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.
Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We’re passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care.
Job Summary
A successful candidate builds and maintains relationships with internal customers while performing thorough repairs, preventative maintenance, and product enhancement activities on highly complex Werfen instrumentation and systems. Responsible to meet Service Delivery Key Performance Indicators while maintaining costs. This position will focus on our Norcross Technology Center Campus. These instruments are used onsite for customer training, production, product investigation lab and technical training labs.
Candidates with previous experience with Electro-Mechanical troubleshooting and repair of complex medical device and/or laboratory diagnostic instruments will be strongly considered. Other professions of interest would be candidate from a hospital or reference lab (MLT, MT, Etc.) that have experience with the preventative maintenance, troubleshooting of diagnostic instruments. We will also strongly consider candidates with military (BMET, TMDE, PMEL, Etc.) experience working on complex systems.
Key Accountabilities
Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.
Networking/Key Relationships
Minimum Knowledge & Experience for the position:
Education: Bachelor's degree (BS/BA) from a four-year college or university; or equivalent combination of education and experience
Management has the discretion of substituting relevant work experience for a degree and/or making exceptions to the years of experience requirement.
Skills & Capabilities
Travel Requirements:
Minimal travel may be required from time to time.
Individual employee compensation will ultimately depend on factors including education, relevant experience, skillset, knowledge, and particular business needs.
This role is eligible for medical, dental, and vision insurance, 401k plan retirement benefits with an employer match, as well as paid vacation and sick leave. Our sales roles are eligible for participation in a commission plan and our management, and select professional roles, are eligible for a performance-based bonus.
If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV.
Werfen is an Equal Opportunity employer and is committed to a diverse workplace. Werfen strictly prohibits unlawful discrimination, harassment or retaliation based upon an individual’s race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process, please contact NAtalentacquisition@werfen.com for assistance.
We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7,000 employees around the world comprise our Werfen team.
www.werfen.com
Sourced by ZipRecruiter
Health care and social assistance
1,001 - 5,000 Employees
L'Hospitalet de Llobregat, Barcelona, ES