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Medical Device Manufacturing Jobs in Reston, VA (NOW HIRING)

... medical device manufacturing sites. This role offers flexibility to work hybrid or fully remote and may require extended hours, regular domestic and international travel, and the ability to work ...

Sr. Manager Data Analytics

Leesburg, VA ยท On-site

$150K - $170K/yr

Proven experience leading Data & Analytics functions in a manufacturing, supply chain, or regulated industry (medical device preferred). * Strong technical expertise with Power BI (semantic models ...

... medical device manufacturing sites. This role offers flexibility to work hybrid or a fully remote arrangement. Candidates should be self-starters, highly organized, and team players. Extended hours ...

Previous experience in aerospace, defense, or medical device manufacturing where high-reliability standards are paramount. The approximate base salary range for this position is $70,852 - $82,661.

... medical device manufacturing sites. This role offers flexibility to work hybrid or a fully remote arrangement. Candidates should be self-starters, highly organized, and team players. Extended hours ...

Cleanroom Assembler

Rockville, MD ยท On-site

$18.25 - $22.50/hr

Accurately document manufacturing activities using Good Documentation Practices (GDP). * Perform all duties within the cleanroom while adhering to gowning requirements and wearing approved Personal ...

Senior Quality Engineer

Sterling, VA ยท On-site

$89K - $121K/yr

Euclid Vision Corporation is a growing medical device organization specializing in orthokeratology ... Partner with engineering, manufacturing, and leadership teams - and build the kind of influence ...

Cleanroom Assembler

MD ยท On-site

$18.25 - $22.50/hr

Accurately document manufacturing activities using Good Documentation Practices (GDP). * Perform all duties within the cleanroom while adhering to gowning requirements and wearing approved Personal ...

Sr. Regulatory Affairs Specialist

Leesburg, VA ยท On-site +1

$100K - $105K/yr

Conduct regulatory assessments for proposed product changes, manufacturing changes, and product ... Working knowledge of US and EU medical device regulations (international experience a plus)

Principal Software Engineer

Germantown, MD ยท On-site

$137K - $184K/yr

... manufacturing and analysis tools. Required Qualifications: * Bachelor's degree in Computer ... Medical device development experience, including familiarity with design controls, risk management ...

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Medical Device Manufacturing information

See Reston, VA salary details

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How much do medical device manufacturing jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for medical device manufacturing in Reston, VA is $28.22, according to ZipRecruiter salary data. Most workers in this role earn between $23.99 and $33.03 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 cities near Reston, VA are hiring for Medical Device Manufacturing jobs?

Cities near Reston, VA with the most Medical Device Manufacturing job openings:

Infographic showing various Medical Device Manufacturing job openings in Reston, VA as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 18% Part Time, 1% Temporary, and 6% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $58,688 per year, or $28.2 per hour.

FDA Technical Consultant

USA Alston & Bird

Washington, DC โ€ข On-site, Remote

Full-time

This job post hasย expired today.ย Applications are no longer accepted.


Job description

Alston & Bird LLP is seeking an experienced FDA consultant to work with the Health Care team's FDA practice out of the Washington, D.C. Office. Qualified candidates will have at least 5 years of experience as an FDA investigator or in a senior global quality role to assist the FDA team in responding to FDA inspections at pharmaceutical and medical device manufacturing sites. This role offers flexibility to work hybrid or fully remote and may require extended hours, regular domestic and international travel, and the ability to work beyond 40 hours per week.

Key Responsibilities

Assist attorneys in supporting manufacturing clients on issues related to Current Good Manufacturing Practices (CGMP) compliance Prepare clients for inspections, provide inspection support (remote and onโ€site) Provide technical support for remediation efforts in response to Form FDA 483s, warning letters, and other enforcement actions Apply extensive knowledge of quality systems, investigations, corrective & preventive actions (CAPAs), contamination control, cleaning validation, and data integrity Collaborate with crossโ€functional teams at the firm and at the client including legal, regulatory, quality, manufacturing, and executive leadership teams Draft memos regarding the status of projects and maintain current accurate daily time records Perform special projects as assigned Skills Needed to be Successful Regular travel within the United States and internationally (1โ€“2 weeks a month with flexibility for more) Ability to organize and prioritize numerous tasks and complete them under time constraints Strong interpersonal skills to communicate and follow instructions effectively from a diverse group of clients, attorneys, and staff Prepared to work more than 40 hours per week and accommodate irregular hours Ability to travel to private and public buildings domestically and internationally via private or public conveyance Education & Experience Bachelor's degree in chemistry, biology, pharmacy, engineering, or a related field. FDA experience required: minimum of 5 years as an FDA investigator or compliance officer, or senior industry position in global quality assurance.

Inโ€depth knowledge of quality systems, regulatory requirements (21 CFR Parts 210, 211 and related guidance), quality management systems (QMS), and ISO standards. Strong analytical skills focused on root cause analysis and problem solving. Excellent written and verbal communication skills. Proficiency in using quality management systems and documentation tools.

Ability to provide exceptional client service and manage multiple engagements in a fastโ€paced environment. Willingness to frequently travel to international and domestic client sites to support inspections, audits, and remediation activities. Salary The salary range for this position in Washington, D.C. is $200,000โ€“$250,000 and represents the firm's goodโ€faith minimum and maximum range for this role at the time of posting.

The actual salary offered will depend on factors such as experience, education, certifications, geographic location, market demands, and business needs. Equal Opportunity Employer Alston & Bird LLP is an Equal Opportunity Employer that does not discriminate on the basis of any status protected under federal, state, or local law.

Applicants will be considered regardless of their sex, race, age, religion, color, national origin, ancestry, physical disability, mental disability, medical condition (associated with cancer, a history of cancer, or genetic characteristics), HIV/AIDS status, genetic information, marital status, sexual orientation, gender, gender identity, gender expression, military and veteran status, or other protected category under the law.