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Locum Medical Device Design Jobs in Virginia (NOW HIRING)

Varsity Tutors

Biomedical Engineering Tutor

Salem, VA · Remote

$18 - $40/hr

Ability to explain signal processing for biosignals, finite element analysis, drug delivery systems, and medical device design principles while preparing students for biomedical engineering ...

Varsity Tutors

Biomedical Engineering Tutor

Fairfax, VA · Remote

$18 - $40/hr

Ability to explain signal processing for biosignals, finite element analysis, drug delivery systems, and medical device design principles while preparing students for biomedical engineering ...

Varsity Tutors

Biomedical Engineering Tutor

Norfolk, VA · Remote

$18 - $40/hr

Ability to explain signal processing for biosignals, finite element analysis, drug delivery systems, and medical device design principles while preparing students for biomedical engineering ...

BSI Group

If you have hands-on experience in the research, design, manufacture or testing of active devices we'd love to hear from you. As a Technical Reviewer, you will work with medical device manufacturers ...

BSI Prof Serv EHS West

If you have hands-on experience in the research, design, manufacture or testing of active devices we'd love to hear from you. As a Technical Reviewer, you will work with medical device manufacturers ...

Addison Group

Senior Staff Packaging Engineer

Leesburg, VA · On-site

$128K - $136K/yr

Lead the design, development, and implementation of sterile and non-sterile medical device packaging systems from concept through production release. * Develop packaging design standards, engineering ...

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Locum Medical Device Design information

What are some common challenges faced by locum medical device design professionals when integrating into new teams and projects?

Locum medical device design professionals often face the challenge of quickly adapting to new team dynamics and project workflows. Since projects may be at various stages of development, locums must rapidly familiarize themselves with existing designs, documentation, and regulatory requirements. Effective communication and collaboration with both engineering and clinical teams are crucial to ensure seamless integration and contribute to project goals. Flexibility and a proactive approach to learning company-specific processes can help locums succeed in these dynamic environments.

What are the key skills and qualifications needed to thrive as a locum medical device design professional?

To thrive as a Locum Medical Device Designer, you need a solid background in biomedical engineering, product design, and regulatory standards, often supported by a relevant degree and prior experience in device development. Familiarity with CAD software, rapid prototyping tools, and knowledge of FDA or CE compliance processes are typically required. Strong problem-solving, adaptability, and effective collaboration skills help individuals excel in varied project environments and short-term assignments. These competencies ensure the delivery of innovative, compliant, and user-centered medical devices within tight timelines.

What is the difference between Locum Medical Device Design vs Contract Medical Device Engineer?

AspectLocum Medical Device DesignContract Medical Device Engineer
CredentialsRelevant engineering degrees, certifications in medical device designSame as locum, often with specialized certifications
Work EnvironmentTemporary assignments in various companies or projectsProject-based, often in corporate or manufacturing settings
Employer & Industry UsageUsed by staffing agencies, hospitals, and medical device firmsEngaged by companies for specific projects or product development

Both roles involve designing medical devices, requiring similar credentials and working in related environments. The key difference is that a locum medical device designer works temporarily across different organizations, while a contract medical device engineer is typically hired for specific projects within a single company.

What is a locum medical device design professional?

Locum medical device design professionals are experts who temporarily fill roles in the design and development of medical devices, often to cover staff shortages or support specific projects. They bring specialized knowledge in engineering, regulatory compliance, and product development, and may be involved in tasks such as prototyping, testing, and documentation. These professionals help companies maintain productivity and meet deadlines without the commitment of a permanent hire. The locum arrangement offers flexibility for both the employer and the professional, and is common in industries requiring highly specialized skills.
What are popular job titles related to Locum Medical Device Design jobs in Virginia? For Locum Medical Device Design jobs in Virginia, the most frequently searched job titles are:
What job categories do people searching Locum Medical Device Design jobs in Virginia look for? The top searched job categories for Locum Medical Device Design jobs in Virginia are:
What cities in Virginia are hiring for Locum Medical Device Design jobs? Cities in Virginia with the most Locum Medical Device Design job openings:
Locum Medical Device Design jobs near you
Infographic showing various Locum Medical Device Design job openings in Virginia as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 19% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution.

Medical Device QMS Auditor

The British Standards Institution (BSI)

Reston, VA • On-site

$98K - $123K/yr

Full-time

Medical, Dental, Life, Retirement, PTO

Re-posted 19 days ago

Job description

We exist to create positive change for people and the planet. Join us and make a difference too!
Job Title: Medical Device QMS Auditor
Location: Candidates must reside in one of the following states: IL, MN, WI, IN, NJ, MA, PA, OH.
BSI (British Standards Institution) is the global business standards company that equips businesses with the solutions to turn standards of best practice into habits of excellence.
Our Medical Devices (or Regulatory Services) team ensures patient safety while supporting timely market access for our clients' medical device products globally. BSI is an accredited ISO 13485 Certification Body recognized in many global markets.
This is a travel based position with extensive travel to medical device manufacutering sites. Candidate must be comfortable with overnight travel of 13-15 days out of every month.
Essential Responsibilities
  • Analyze and assess quality management systems with emphasis on design controls, manufacturing controls, production processes, process validation, verification/validation, and testing activities, ensuring compliance with ISO 13485, CE Marking, and MDSAP schemes.
  • Assess manufacturing processes including production controls, process validation, risk management, supplier controls, and design transfer activities.
  • Prepare assessment reports and communicate findings to clients, providing clear direction for corrective actions where appropriate.
  • Recommend the issue, re-issue, or withdrawal of certificates in accordance with BSI policies and procedures.
  • Lead assessment teams, ensuring quality of service and effective working relationships with clients and team members.

Education & Technical Qualifications
  • Technical degree (Bachelor's, or higher) in Engineering, Science, or a related technical discipline required. Relevant fields include Biomedical, Mechanical, Electrical, or Chemical Engineering; Materials Science; Biology; Microbiology; Chemistry; or related technical fields applicable to medical devices, SaMDs, or IVDs.
  • Minimum of 4 years' experience in the medical device, SaMD, or IVD fields with direct, hands-on involvement in designing, manufacturing, validating, inspecting, testing, or clinically evaluating devices. Candidates must have personally worked with devices, specifications, or code, indicate the types and classifications of devices, and demonstrate their level of involvement on their CV. Regulatory or audit experience only is insufficient.
  • Detailed hands-on experience with design and manufacturing/production controls, including process validation (IQ/OQ/PQ), risk management, supplier controls, CAPA, nonconforming product management, and change control.
  • Knowledge of regulatory requirements and quality management standards including ISO 13485, MDSAP, FDA QSR (21 CFR 820), and EU MDR/IVDR are a plus

Core Competencies
  • Strong verbal and written communication skills, and attention to detail.
  • Ability to work under pressure and meet deadlines.
  • Self-motivated, flexible, and excellent time management/planning skills.
  • Willingness to travel extensively.
  • Enthusiastic, committed team player.
  • Business development and public speaking skills are considered advantageous.

Preferred Qualifications
  • Experience with process validation, equipment qualification, and manufacturing process development.
  • Experience in design and development activities, including design controls and design transfer.
  • Hands-on experience with software-controlled medical devices, SaMD, or automated manufacturing systems.
  • Experience auditing or assessing quality management systems compliant with ISO 13485, CE Marking, and MDSAP.
  • Experience with risk management (ISO 14971), sterile medical devices, aseptic processing, or cleanroom manufacturing.
  • Experience leading hands-on teams in manufacturing, testing, or validation.
  • Lead Auditor certification (ISO 13485, MDSAP, or equivalent) preferred.
  • Previous experience working for a Notified Body, Regulatory Body, or Certification Body preferred.
  • Advanced degree (MS, PhD) in engineering, science, or related technical discipline preferred.

The salary for this position can range from $98,100 to $123,860 annually; actual compensation is based on various factors, including but not limited to, the candidate's competencies, level of experience, education, location, divisional budget and internal peer compensation comparisons. BSI offers a competitive salary, group-sponsored health and dental, short-term and long-term disability, a company-matched 401k plan, company paid life insurance, 11 paid holidays and 4 weeks paid time off.
#LI-REMOTE
#LI-MS1
About Us
BSI is a business improvement and standards company and for over a century BSI has been recognized for having a positive impact on organizations and society, building trust and enhancing lives.
Today BSI partners with more than 77,500 clients in 195 countries and engages with a 15,000 strong global community of experts, industry and consumer groups, organizations and governments.
Utilizing its extensive expertise in key industry sectors - including automotive, aerospace, built environment, food and retail, and healthcare - BSI delivers on its purpose by helping its clients fulfil theirs.
Living by our core values of Client-Centricity, Agility, and Collaboration, BSI provides organizations with the confidence to grow by partnering with them to tackle society's critical issues - from climate change to building trust in digital transformation and everything in between - to accelerate progress towards a better society and a sustainable world.
BSI is an Equal Opportunity Employer dedicated to fostering a diverse and inclusive workplace.

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