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Medical Device Product Development Jobs in Virginia

Caraballo Consulting & Associates L

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QA Manufacturing Engineer - Medical Device

Sterling, VA · On-site

$40 - $80/hr

... production floor. * Ability to work independently while coordinating effectively with cross ... Medical Device, Pharmaceutical, and Biotec industries, finding qualified personnel.

Caraballo Consulting & Associates L

Be Seen First

QA Manufacturing Engineer - Medical Device

Sterling, VA · On-site

$40 - $80/hr

... production floor. * Ability to work independently while coordinating effectively with cross ... Medical Device, Pharmaceutical, and Biotec industries, finding qualified personnel.

VB Spine

Staff Engineer

Leesburg, VA · On-site

$128 - $136/hr

Bachelor of Science in Mechanical Engineering, Biomedical Engineering, or related discipline (Master's preferred) * 4+ years of medical device product development experience * Strong technical ...

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Medical Device Product Development information

What is a medical device product development?

A Medical Device Product Development job involves designing, testing, and bringing medical devices to market while ensuring compliance with regulatory standards. Professionals in this role work with cross-functional teams, including engineering, regulatory affairs, and manufacturing, to develop safe and effective healthcare solutions. They oversee the entire product lifecycle, from concept and prototyping to clinical validation and commercialization. Strong knowledge of FDA, ISO, and other regulatory requirements is essential.

What are some typical challenges faced in medical device product development roles?

Professionals in Medical Device Product Development often encounter challenges such as navigating complex regulatory requirements, managing cross-functional project teams, and ensuring that products meet both clinical needs and quality standards. Balancing innovative design with safety and compliance can require careful planning and solid problem-solving skills. Additionally, adapting to shifting project timelines and incorporating stakeholder feedback are common aspects of the job. Overcoming these challenges is rewarding and helps ensure the delivery of safe, effective devices to patients and healthcare providers.

What are the key skills and qualifications needed to thrive in medical device product development?

To thrive in Medical Device Product Development, you need a strong background in engineering or life sciences, product design, and an understanding of regulatory requirements like FDA and ISO standards. Proficiency with CAD software, project management tools, and knowledge of quality management systems (QMS) is commonly required, along with certifications such as Six Sigma or PMP being beneficial. Strong problem-solving abilities, collaboration skills, and effective communication are key soft skills for this role. These skills are important to ensure that devices are developed safely, efficiently, and in compliance with industry regulations while fostering innovation and teamwork.

What are popular job titles related to Medical Device Product Development jobs in Virginia?

For Medical Device Product Development jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Medical Device Product Development jobs in Virginia look for?

The top searched job categories for Medical Device Product Development jobs in Virginia are:

What cities in Virginia are hiring for Medical Device Product Development jobs?

Cities in Virginia with the most Medical Device Product Development job openings:

Medical Device Product Development jobs near you
Infographic showing various Medical Device Product Development job openings in Virginia as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, and 5% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution.

QA Manufacturing Engineer - Medical Device

Caraballo Consulting & Associates L

Sterling, VA • On-site

$40 - $80/hr

Contractor

Posted 17 days ago

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Job description

We are seeking a Quality Manufacturing Engineer extensive experience in Medical Devices to oversee Manufacturing Quality projects and line transfers for a Medical Device company.  The perfect candidate will perform the following activities:

Key Responsibilities:

    • Support quality assurance activities associated with transferring and starting up manufacturing operations at the new site.
    • Review, execute, and approve validation documentation, including protocols, test scripts, test data, and final reports.
    • Provide QA oversight for process validation activities to ensure processes are qualified, controlled, and appropriately documented.
    • Support equipment qualification efforts, including IQ, OQ, and PQ activities for manufacturing equipment and related systems.
    • Partner with Manufacturing, Engineering, Validation, and Quality teams to ensure validation deliverables are completed on time and in compliance with applicable procedures and regulations.
    • Assess validation packages for completeness, accuracy, traceability, and adherence to GMP and medical device quality system requirements.
    • Support investigation and resolution of validation-related deviations, discrepancies, and change controls.
    • Generate, review, and approve validation summary reports and supporting documentation for management and quality records.                  
    • Support QA activities associated with the QMS integration of 2 companies.
    • Modify SOPs to complete QMS integration.
    • Complete Change Control activities.
    • Complete the bulk download of documents and records from a Quality Management System.

   Required Qualifications:

  • Bachelor’s degree in Engineering, Quality, Life Sciences, or a related technical discipline, or equivalent relevant experience.
  • Experience in the medical device industry within Quality Assurance, Validation, Manufacturing Quality, or a closely related function.
  • Strong working knowledge of process validation, equipment qualification, and GMP requirements in a regulated manufacturing environment.
  • Demonstrated experience reviewing and approving validation documentation and technical reports.
  • Familiarity with manufacturing operations and the practical application of quality requirements on the production floor.
  • Ability to work independently while coordinating effectively with cross-functional stakeholders.
  • Strong technical writing, documentation review, and problem-solving skills.
  • Excellent attention to detail and ability to manage multiple priorities within a time-bound project.

Company Description

We are a specialized Global staffing firm that works for Fortune 500 companies in the Medical Device, Pharmaceutical, and Biotec industries, finding qualified personnel.