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Medical Device Operations Jobs in Virginia (NOW HIRING)

Zimmer, Inc.

Senior Quality Manager

Fairfax, VA · On-site

$130K - $160K/yr

... medical device design and manufacturing site. Utilizes quality statistics to develop effective ... improve operational efficiencies, ensuring seamless integration of quality in all aspects of ...

Zimmer, Inc.

Senior Quality Manager

Virginia Beach, VA · On-site

$130K - $160K/yr

... medical device design and manufacturing site. Utilizes quality statistics to develop effective ... improve operational efficiencies, ensuring seamless integration of quality in all aspects of ...

Zimmer, Inc.

Senior Quality Manager

Richmond, VA · On-site

$130K - $160K/yr

... medical device design and manufacturing site. Utilizes quality statistics to develop effective ... improve operational efficiencies, ensuring seamless integration of quality in all aspects of ...

Owens & Minor, Inc.

Operations Manager

Ashland, VA · On-site

$110K/yr

Bachelor's degree required. * 9 or more years of professional supply chain or warehouse operations experience, preferably within the healthcare/medical/medical device industry. * Previous supervisory ...

Owens & Minor

Operations Manager

Ashland, VA

$110K/yr

Bachelor's degree required. * 9 or more years of professional supply chain or warehouse operations experience, preferably within the healthcare/medical/medical device industry. * Previous supervisory ...

Fortis Surgical

Director of Operations

Glen Allen, VA · On-site

$100K - $120K/yr

Experience supporting regulated healthcare or medical device environments * Strong project ... The Director of Operations will be constantly interacting, problem solving, and adapting to the ...

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Medical Device Operations information

What is the difference between Medical Device Operations vs Medical Device Quality Assurance?

AspectMedical Device OperationsMedical Device Quality Assurance
Primary FocusManaging manufacturing, supply chain, and product deploymentEnsuring product quality, compliance, and safety standards
Required CertificationsRegulatory knowledge, manufacturing certificationsQuality management certifications, ISO standards
Work EnvironmentManufacturing plants, supply chain settingsQuality labs, compliance departments
Industry UsageUsed across production and logistics teamsUsed within quality control and regulatory teams

Medical Device Operations and Medical Device Quality Assurance roles often overlap but focus on different aspects of the product lifecycle. Operations centers on manufacturing and logistics, while Quality Assurance emphasizes compliance and safety. Both roles require regulatory knowledge and are essential in the medical device industry.

What are some common challenges faced by professionals in Medical Device Operations, and how can they be addressed?

Professionals in Medical Device Operations often face challenges related to maintaining strict regulatory compliance, ensuring product quality, and managing cross-functional communication between manufacturing, quality assurance, and regulatory teams. Staying up to date with changing FDA or international regulations is essential, and frequent documentation or process audits can be demanding. Building strong organizational habits, leveraging digital tracking tools, and fostering open communication channels with other departments can help address these challenges and ensure smooth operations.

What are medical device operations?

Medical device operations refer to the processes and activities involved in the manufacturing, assembly, quality control, supply chain management, and distribution of medical devices. This field ensures that devices are produced efficiently, meet regulatory standards, and are delivered safely to healthcare providers and patients. Operations teams collaborate with engineering, quality assurance, and regulatory departments to maintain compliance and optimize production workflows. Their work is crucial for ensuring that medical devices are safe, effective, and readily available for patient care.

What are the key skills and qualifications needed to thrive in Medical Device Operations, and why are they important?

To thrive in Medical Device Operations, you need a solid understanding of regulatory compliance, quality assurance, and supply chain management, often supported by a degree in engineering, life sciences, or business. Familiarity with quality management systems (QMS), FDA regulations, and software like ERP systems is typically required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for coordinating cross-functional teams and ensuring compliance. These competencies are vital for delivering safe, high-quality medical devices efficiently and in accordance with rigorous industry standards.
What are popular job titles related to Medical Device Operations jobs in Virginia? For Medical Device Operations jobs in Virginia, the most frequently searched job titles are:
What job categories do people searching Medical Device Operations jobs in Virginia look for? The top searched job categories for Medical Device Operations jobs in Virginia are:
What cities in Virginia are hiring for Medical Device Operations jobs? Cities in Virginia with the most Medical Device Operations job openings:
Medical Device Operations jobs near you
Infographic showing various Medical Device Operations job openings in Virginia as of July 2026, with employment types broken down into 77% Full Time, 15% Part Time, and 8% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution.

Senior Quality Manager

Zimmer, Inc.

Fairfax, VA • On-site

$130K - $160K/yr

Other

Posted 18 days ago

Job description

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging.


What You Can Expect


This is an onsite role at our site in Norfolk, Virginia
Site Quality leader and Management Representative responsible for directing the quality function a medical device design and manufacturing site. Utilizes quality statistics to develop effective strategies to maintain and improve the performance of products and the quality system. Develops relationships with key development and manufacturing peers to identify emerging needs. Resolves complex problems that have implications beyond own area. Requires professional expertise and interpersonal skills to manage multiple projects and interface with personnel from all company disciplines and business units. Takes accountability, achieves results and develops self and others.

How You'll Create Impact
  • Develop and implement site-wide quality strategy aligned with corporate objectives and regulatory requirements (QMSR, GMP, ISO, and other global standards) including objectives, and planning to support the strategy.
  • Establish and refine key quality metrics, ensuring data-driven decision-making to enhance product integrity and regulatory compliance.
  • Partner with R&D, supply chain, manufacturing, and distribution teams to enhance quality processes across the product lifecycle and drive cross-functional teamwork to improve operational efficiencies, ensuring seamless integration of quality in all aspects of pharmaceutical production.
  • Serve as the primary quality representative during regulatory inspections and audits, ensuring adherence to industry and corporate standards.
  • Build, mentor, and lead a high-performing quality assurance and quality control (QA/QC) team, fostering a culture of collaboration and accountability.
  • Empower team to lead investigations into deviations, CAPA (Corrective and Preventive Actions), and change control processes to improve operational resilience and ensure timely product release and market supply by resolving quality-related issues effectively
What Makes You Stand Out
  • Must have a thorough knowledge of QMSR, GMP, ISO and other relevant regulatory requirements as applied to medical device development, manufacturing and distribution.
  • Demonstrated independent decision-making ability applying regulations and standards related to the manufacturing and distribution of medical device products.
  • Demonstrated management ability including organizational design and employee selection, development, motivation and performance.
  • Demonstrated ability to achieve productivity goals collaboratively without sacrificing quality in a manufacturing environment.
  • Demonstrated understanding of interactions and interdependency of elements within the quality system in a pharmaceutical manufacturing organization.
  • Must be able to work with all levels of employees, including hourly production employees through senior management.
  • Must possess excellent written and oral communication skills and the demonstrated ability to communicate with individuals of varying backgrounds.
Your Background
  • A Bachelor's Degree in a technical field is required
  • 7-10 years of work experience in medical device quality, preferably in manufacturing environments
  • 5 years' experience with direct management responsibility
  • CQE/CQM preferred


Expected Compensation: $130,000- $160,000 base salary. Role also comes with a comprehensive bonus.


EOE

Employment Type: OTHER

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