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Medical Device Assembler

Maple Plain, MN · On-site

$24/hr

Medical Device Assembler Location: Maple Plain, MN 55359 Duration: Contract Shift: M-F 7:30AM-4PM ... In all actions, this person shall demonstrate a primary commitment to patient safety and product ...

Anonymous Employer

Med-Device Assembler

Providence, RI

$21 - $23/hr

**Job Title: **Med-Device Assembler (x2) **Pay Rate: **$21-$23/hr. ($21/hr. without soldering $23/hr ... Maintain a clean and organized work area to ensure safety and device quality * Escalate issues and ...

Astrix Inc

Medical Device Assembler

Trumbull, CT · On-site

$17.75 - $21.50/hr

Maintain a clean and organized work area while following required safety and cleanliness protocols ... supervisors Medical Device Assembler Qualifications/Requirements: * High school diploma or ...

VOLT

Medical Device Assembler

Plymouth, MN · On-site

$17.50 - $19.25/hr

Maintain cleanroom protocols and adhere to all safety procedures * Perform repetitive fine motor ... Experience as a Medical Device Assembler or Production Assembler. * Strong attention to detail ...

VOLT

Medical Device Assembler

Irvine, CA · On-site

$18 - $19.75/hr

Adhere to all safety procedures and cleanroom protocols. * Perform repetitive manual tasks such as ... Prior experience as a Medical Device Assembler or Production Assembler preferred. * Previous ...

Kelly Services

Medical Device Assembler

Irvine, CA · On-site

$24/hr

As a Medical Device Assembler, you will play a key role in developing and assembling innovative ... Maintain compliance with GMP, ISO, SOP, and safety guidelines. * Maintain clean and organized ...

VOLT

Medical Device Assembler

Irvine, CA · On-site

$18 - $19.67/hr

Adhere to all safety procedures and cleanroom protocols. * Perform repetitive manual tasks such as ... Prior experience as a Medical Device Assembler or Production Assembler preferred. * Previous ...

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$12

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How much do medical device safety jobs pay per hour?

As of Jul 22, 2026, the average hourly pay for medical device safety in the United States is $49.14, according to ZipRecruiter salary data. Most workers in this role earn between $38.46 and $55.53 per hour, depending on experience, location, and employer.

What are the main challenges faced in a Medical Device Safety role?

Professionals in Medical Device Safety often navigate complex regulatory landscapes while managing multiple safety evaluations and incident reports. Common challenges include staying updated with evolving compliance standards, communicating technical findings to cross-functional teams, and ensuring timely risk mitigation when issues arise. The role requires balancing in-depth technical analysis with clear, concise reporting for both internal stakeholders and external agencies. While the work can be demanding, it is highly rewarding, as you'll play a critical part in protecting patient health and supporting the safe use of innovative healthcare technologies.

What are the key skills and qualifications needed to thrive in the Medical Device Safety position, and why are they important?

To thrive in Medical Device Safety, you need knowledge of biomedical engineering, regulatory compliance, risk assessment, and incident investigation, usually backed by a degree in a related field such as engineering, life sciences, or healthcare. Familiarity with regulatory frameworks like FDA, ISO 13485, and tools such as safety reporting systems and risk management software is essential. Strong analytical thinking, detail orientation, and effective communication skills enable successful collaboration and reporting across clinical and technical teams. These skills ensure patient safety, regulatory compliance, and the continued efficacy of medical devices in healthcare environments.

What is a Medical Device Safety job?

A Medical Device Safety job focuses on ensuring the safety, effectiveness, and regulatory compliance of medical devices. Professionals in this field monitor adverse events, analyze risks, and collaborate with regulatory agencies to maintain patient safety. They may also develop safety protocols, conduct investigations, and provide recommendations for corrective actions. This role is essential in protecting patients and meeting industry standards.

More about Medical Device Safety jobs
What cities are hiring for Medical Device Safety jobs? Cities with the most Medical Device Safety job openings:
What states have the most Medical Device Safety jobs? States with the most job openings for Medical Device Safety jobs include:
What job categories do people searching Medical Device Safety jobs look for? The top searched job categories for Medical Device Safety jobs are:
Medical Device Safety jobs near you
Infographic showing various Medical Device Safety job openings in the United States as of July 2026, with employment types broken down into 77% Full Time, 14% Part Time, and 9% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $102,217 per year, or $49.1 per hour.
Senior Manager Medical Device Safety, Pharmacovigilance

Senior Manager Medical Device Safety, Pharmacovigilance

Us tech Solutions

Whippany, NJ

Contractor

Re-posted 24 days ago

Job description

Company Description

US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website http://www.ustechsolutions.com/.We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, and we currently have a job opening that may interest you

Job Description

Title: Senior Manager Medical Device Safety, Pharmacovigilance

Duration: 12 Months

Location: Whippany, NJ 07981

 

Job Description:

The Senior Manager Medical Device Safety (MDS) carries out global Pharmacovigilance (PV) business processes and analyses/trends safety data sets related to complaint handling, regulatory reporting and clinical development for Company medical devices and combination products. The Senior Manager MDS is an expert who provides safety oversight and content contributions to design control, clinical evaluations, vigilance reporting to authorities, trending and post-marketing surveillance for Company Pharmaceutical and Consumer Health medical devices and combination products worldwide.

Position summary:

The incumbent provides counsel as PV medical device subject matter expert to ensure that an effective vigilance, post-marketing surveillance (PMS) and trending systems are implemented and maintained which conforms with global requirements/laws. The Senior Manager MDS works cross-functionally to generate solutions and implement process standards consistent with device industry best practices. The incumbent is a strong problem solver and communicator with a solid understanding of global regulations and standards.

The incumbent will be responsible for the production and accuracy of medical device analysis, interpretation of results and content contributions to PMS and Vigilance activities.

Position duties & responsibilities:

Provide content input to Project teams for designing, planning and conducting analyses of safety data for the assessment of medical device safety and performance.

Provide content input to the post-marketing surveillance (PMS) program activities including, PMS system documentation, PMS planning and report management.

Provide content input, develop and execute PMS trending methodologies, analysis, written contributions and trend report preparations.

Responsible for monitoring, analyzing and applying trending methodologies to the vigilance data submitted to Health Authorities (e.g MDRs).

Responsible for the production and accuracy of medical device analysis and interpretation of results.

Independently review large data sets and prepare reports for submission the Health Authorities under strict timelines and resolved respective queries regarding product safety.

Qualifications

Requirements/Preferences

Education Requirement(s):

Bachelor's Degree in Engineering, Mathematics or Life-science Discipline with 4 years of professional experience in medical devices or similar sector

Skill & Competency Requirements:

Strong scientific application of statistical methods used for evaluating complaint trends and establishing thresholds for routine trend reviews (e.g. human factor, malfunction, user interface and user safety)

Background in medical device trending/signal detection and heavy statistical analysis experience.

Able to develop and administer management information systems for track and trending.

Strong analytical and technical skills that include data collection, analysis and required report generation

Strong communication skills and ability to work both, independently and cross-functionally with Quality, Regulatory, Marketing and other applicable functions within the business

Working understanding of medical device regulations and industry standards globally specifically 21 CFR 820, 803, ISO 13485, and euMDR 2017/745

Preferences:

The individual should be comfortable working in both office/virtual settings and independently.

Additional Information

All your information will be kept confidential according to EEO guidelines.

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About US Tech Solutions

Sourced by ZipRecruiter

US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions.

Industry

It services

Company size

1,001 - 5,000 Employees

Headquarters location

Jersey City, NJ, US

Year founded

2000

Social media

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