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Fda Inspector Jobs in Massachusetts (NOW HIRING)

Quality Inspector Technician Department: Quality Employment Type: Full Time Location: Burlington ... FDA - GMP experience and training a plus. * Technical training and/or certifications a plus.

We are searching for a Quality Inspector to be responsible for testing materials and finished ... Knowledge and experience with GMP, ISO, FDA, and quality standards * Experience in a clean room ...

Manager, Technical Complaints

Boston, MA · Hybrid

$110K - $143K/yr

Support FDA inspections, notified body audits and global regulatory inspections. * Collaborate across Medical Safety, Regulatory Affairs, Engineering, Manufacturing, Patient Experience and Global ...

S. FDA inspections and direct support for EU Notified Body audits and ROW competent authority inspections. Organizational Leadership & Regulatory Excellence * Mentor and develop regulatory team ...

S. FDA inspections and direct support for EU Notified Body audits and ROW competent authority inspections. Organizational Leadership & Regulatory Excellence * Mentor and develop regulatory team ...

Knowledge of ISO 13485 and FDA regulations * Experience with First Article Inspection (FAI) documentation * Familiarity with nonconformance and corrective action processes * Strong problem-solving ...

Serve as the primary on-site liaison during FDA inspections in coordination with global regulatory teams. * Prepare for, host, and respond to regulatory inspections and external audits. * Conduct and ...

Showing results 21-40

Fda Inspector information

See Massachusetts salary details

$26.8K

$60K

$108.1K

How much do fda inspector jobs pay per year?

As of Aug 14, 2026, the average yearly pay for fda inspector in Massachusetts is $60,000.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,000.00 and $69,300.00 per year, depending on experience, location, and employer.

What types of facilities or products do FDA inspectors review, and what does a typical inspection process involve?

FDA Inspectors routinely examine a variety of facilities, such as food processing plants, pharmaceutical manufacturers, medical device companies, and cosmetic production sites, to ensure compliance with federal safety and quality regulations. A typical inspection involves reviewing operational procedures, examining production environments, sampling products, and interviewing staff to identify potential violations or risks. Inspectors often work onsite, sometimes with travel required to cover multiple locations within their region, and collaborate closely with facility management to explain findings and recommend corrective actions. This role offers the opportunity to make a significant impact on public health and provides clear advancement pathways into specialized inspection or supervisory roles within regulatory agencies.

What skills and qualifications are needed to be an FDA inspector?

To thrive as an FDA Inspector, you need a solid background in science or public health, attention to detail, and thorough knowledge of regulatory standards, often supported by a relevant degree. Familiarity with inspection protocols, laboratory testing equipment, and digital reporting systems is commonly required, along with potential USDA or FDA certifications. Strong analytical thinking, effective communication, and integrity are important soft skills for this role. These competencies ensure accurate inspections, compliance with safety regulations, and clear reporting essential to public health and organizational accountability.

How do you become an FDA inspector?

To become an FDA inspector, candidates typically need a bachelor's degree in a relevant field such as biology, chemistry, or food science, along with experience in food safety, pharmaceuticals, or related areas. They must pass the FDA's specialized training program and often require a background check and security clearance; some positions may also require state licensure or certifications. Strong attention to detail, knowledge of regulatory standards, and good communication skills are essential for the role.

What does an FDA inspector do?

An FDA Inspector is responsible for ensuring that companies comply with federal regulations related to food, drugs, medical devices, and other products overseen by the U.S. Food and Drug Administration. They conduct inspections, review records, collect samples, and assess manufacturing practices to ensure public health and safety. Inspectors may also investigate complaints, issue compliance notices, and recommend enforcement actions if violations are found.

What are popular job titles related to Fda Inspector jobs in Massachusetts?

For Fda Inspector jobs in Massachusetts, the most frequently searched job titles are:

Infographic showing various Fda Inspector job openings in Massachusetts as of August 2026, with employment types broken down into 73% Full Time, 13% Part Time, 13% Contract, and 1% Nights. Highlights an 97% Physical, and 3% Remote job distribution, with an average salary of $60,000 per year, or $28.8 per hour.

Quality Inspector Technician

Myomo, Inc

Burlington, MA • On-site

$26 - $28/hr

Full-time

Posted 16 days ago


Job description

Quality Inspector Technician
Department: Quality
Employment Type: Full Time
Location: Burlington, MA
Compensation: $26.00 - $28.00 / hour
Description
Why should you join our success story?
Based on patented technology developed at MIT, Harvard Medical School and by the Company, Myomo develops and markets the MyoPro® product line of lightweight, non-invasive, powered arm braces (orthoses) to restore function in paralyzed or weakened arms and hands of individuals that have suffered a stroke, spinal cord, or nerve injury. (E.g. brachial plexus injury or other neuro-muscular disabilities.) It is the only device that, sensing a patient's own neurological signals through non-invasive wearable sensors, can restore the ability to use their arms and hands so that they can live independently, increase their quality of life, reduce cost of care, and return to work. Published clinical research shows a clinically significant instantaneous reduction in upper extremity impairment with the MyoPro. Our technology has been referred by leading-edge rehabilitation facilities including Mayo Clinic, Kennedy Krieger Institute, Cleveland Clinic, Loma Linda Medical Center, Massachusetts General Hospital, numerous VA Hospitals, and more. Myomo is headquartered in Burlington, Massachusetts, with sales and clinical professionals across the U.S.
What we're looking for:
The core responsibility of the Quality Inspector Technician role is to perform quality inspections while providing overall support to both Quality and cross-functional departments/stakeholders as necessary.
Additional responsibilities include conducting inspection of incoming orthosis design components, mid-process checks, and a final outgoing inspection on devices prior to shipment. The Quality Inspector Technician will initiate NCMRs for nonconforming materials and devices, offering testing support to quality and engineering as well.
The ideal candidate is a process-oriented, and systematic-minded professional with both previous regulatory compliance background as well as an appreciation for consistency, standardization, and accuracy. He/she will demonstrate strong attention to detail as well as the capability to thrive an evolving environment, all while driving back to processes and procedures.
How You'll Drive Impact:
  • Conduct inspection of incoming product components.
  • Initiate NCMRs for nonconforming materials; conducting data collection and testing for NCMRs as appropriate.
  • Ability to sort materials and components as needed.
  • Assist with rework, device servicing, and repairs. (NCMRs)
  • Perform in-process quality inspections and checks, as well as final inspection and device testing prior to outgoing shipments.
  • Provide quality support to New Product Development, as well as execution of tasks and assignments for QC Manager on an ad hoc basis.

What You'll Bring:
  • 2+ years' electro-mechanical device quality inspection background within the medical device industry, or similar.
  • Familiarity with components, materials testing, inspection tools, product rework, and equipment.
  • Strong attention to detail and a disciplined work ethic.
  • High school diploma or GED required. Some college may be a plus.
  • FDA - GMP experience and training a plus.
  • Technical training and/or certifications a plus.
  • Teamwork-oriented mindset with the ability to follow work instructions and procedures systematically as well as a capability to complete and submit documentation accurately and promptly.