ZipRecruiter

Log In

1

Medical Device Manufacturing Jobs in Virginia (NOW HIRING)

Mirion

Continuous Improvement Manager

Norfolk, VA · On-site

$91K - $122K/yr

... medical device manufacturing organization. This role champions Lean, Six Sigma, and problem-solving methodologies to improve product quality, reduce waste, enhance cost efficiency, and ensure ...

Addison Group

Senior Staff Packaging Engineer

Leesburg, VA · On-site

$128K - $136K/yr

Leesburg, VA (5-15% Travel) Compensation: $128,000 - $136,000 Base Salary + Performance Bonus Potential Company Overview Our client is a leading privately held medical device manufacturer focused on ...

Pop-Up Talent

Principal QAE

Charlottesville, VA · On-site

$112K - $136K/yr

At least 8+ years of Quality Assurance/Quality Engineering experience in medical device manufacturing * Experience with mechanical and electrical products * ASQ Certified Quality Engineer (CQE) or ...

Aurora Lifesciences

QC Team Lead

Manassas, VA · On-site

$90 - $120/hr

Experience in medical device manufacturing is desirable. * Previous experience in a team leader, supervisory, or shift leadership role. * Working knowledge of ISO 13485, EU MDR, and FDA 21 CFR Part ...

New

previous pagenext page

Showing results 21-40

All JobsMedical Device Manufacturing JobsMedical Device Manufacturing Jobs in Virginia

Medical Device Manufacturing information

See Virginia salary details

$18

$26

$39

How much do medical device manufacturing jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for medical device manufacturing in Virginia is $26.89, according to ZipRecruiter salary data. Most workers in this role earn between $22.88 and $31.44 per hour, depending on experience, location, and employer.

What is a medical device manufacturing job?

A Medical Device Manufacturing job involves producing, assembling, and testing medical devices to ensure they meet regulatory and quality standards. Workers in this field may operate machinery, inspect products, and follow strict guidelines to maintain safety and efficiency. Roles can range from machine operators and quality control inspectors to engineers and regulatory compliance specialists. This industry is essential for creating devices like surgical instruments, pacemakers, and diagnostic equipment used in healthcare. Attention to detail, adherence to regulations, and technical skills are key for success in this field.

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

To thrive in Medical Device Manufacturing, you need strong attention to detail, knowledge of quality assurance processes, and an understanding of regulatory standards such as ISO 13485 or FDA requirements. Experience with manufacturing equipment, ERP systems, and specialized tools for assembly and testing is typically required, and certification in areas like Six Sigma or Lean Manufacturing can be advantageous. Effective communication, teamwork, and problem-solving skills help individuals excel in fast-paced, multidisciplinary environments. These skills are vital for maintaining product safety, ensuring regulatory compliance, and meeting production targets in the highly regulated medical device industry.

What career advancement opportunities are available in medical device manufacturing?

Medical Device Manufacturing offers a variety of career advancement paths, allowing employees to move into roles such as production supervisor, quality assurance specialist, or process engineer as they gain experience. Many companies provide on-the-job training, mentorship programs, and support for additional certifications to help employees further develop their technical and leadership skills. Team members who demonstrate strong performance and a commitment to continuous improvement may also transition into management positions or cross-functional roles in research and development, regulatory affairs, or supply chain management. This field values both specialized technical expertise and a proactive approach to professional growth, providing long-term career stability and diverse opportunities.

Is medical device manufacturing a good career?

Medical device manufacturing is a stable career that involves assembling, testing, and quality control of medical equipment, often requiring technical skills and certifications. It offers opportunities for advancement and typically provides a clean, regulated work environment, with demand driven by healthcare industry growth.

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

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

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

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

What cities in Virginia are hiring for Medical Device Manufacturing jobs?

Cities in Virginia with the most Medical Device Manufacturing job openings:

Medical Device Manufacturing jobs near you
Infographic showing various Medical Device Manufacturing 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, with an average salary of $55,928 per year, or $26.9 per hour.

Continuous Improvement Manager

Phase2 Technology

Norfolk, VA • On-site

$100 - $140/hr

Other

Posted 3 days ago

New

Job description

Description

The Continuous Improvement Manager is responsible for leading, developing, and executing strategies to drive operational excellence across the medical device manufacturing organization. This role champions Lean, Six Sigma, and problemsolving methodologies to improve product quality, reduce waste, enhance cost efficiency, and ensure regulatory compliance. The Continuous Improvement Manager partners closely with Manufacturing, Quality, Engineering, Supply Chain, and Regulatory Affairs to standardize processes and cultivate a culture of continuous improvement.

Key Responsibilities Continuous Improvement Leadership
  • Develop and implement sitewide continuous improvement strategies aligned with business goals.
  • Facilitate Kaizen events, value stream mapping, root cause analysis (RCA), and other improvement workshops.
  • Mentor and train employees at all levels in CI tools, Lean thinking, and structured problem-solving.
  • Establish systems to monitor, measure, and report CI progress and KPIs.
Process Optimization & Waste Reduction
  • Analyze production and quality performance to identify opportunities for efficiency, cost reduction, and throughput improvements.
  • Drive initiatives using DMAIC, PDCA, 5S, standard work, and other Lean/Six Sigma methodologies.
  • Collaborate with cross-functional teams to streamline workflows, enhance equipment utilization, and improve material flow.
Quality & Regulatory Compliance
  • Ensure improvement projects support and strengthen compliance with FDA regulations (21 CFR Part 820), ISO 13485, and internal QMS requirements.
  • Partner with Quality teams to reduce defect rates, CAPA recurrence, and manufacturing variation.
  • Use data-driven approaches to ensure process capability, validation support, and risk mitigation.
Project Management
  • Plan, execute, and sustain mediumtolarge scale CI projects, ensuring milestones are met.
  • Develop business cases, project charters, and ROI analyses to justify improvement initiatives.
  • Present CI updates, outcomes, and recommendations to senior leadership.
Culture & Capability Building
  • Promote a culture of operational excellence and accountability throughout the organization.
  • Create and maintain training materials, SOPs, and standardized processes.
  • Coach teams to identify waste, solve problems autonomously, and embrace continuous learning.
Required Qualifications
  • Bachelor's degree in Engineering, Manufacturing, Operations, or related field.
  • 5+ years of experience in continuous improvement, operational excellence, or process engineering within a regulated manufacturing environment (medical device preferred).
  • Strong working knowledge of Lean, Six Sigma, and structured problem-solving tools.
  • Experience working within FDA-regulated or ISO 13485 environments.
  • Demonstrated success leading CI projects and cross-functional teams.
  • Excellent analytical, communication, facilitation, and changemanagement skills.
  • Familiarity with statistical software (Minitab, JMP, etc.).
  • Experience with automation, digital manufacturing tools, or Industry 4.0 technologies.

Equal Opportunity Employer

This employer is required to notify all applicants of their rights pursuant to federal employment laws.

For further information, please review the Know Your Rights notice from the Department of Labor.

#J-18808-Ljbffr

Apply