Job Title: Medical Device Engineer Support the development, validation, and optimization of ... Analyze experimental data. * Support engineering change control processes. Essential Skills
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Job Title: Medical Device Engineer Support the development, validation, and optimization of ... Analyze experimental data. * Support engineering change control processes. Essential Skills
Quick apply
Job Title: Medical Device Engineer Support the development, validation, and optimization of ... Analyze experimental data. * Support engineering change control processes. Essential Skills
Whippany, NJ 07981 The Senior Manager Medical Device Safety (MDS) carries out global Pharmacovigilance (PV) business processes and analyses/trends safety data sets related to complaint handling ...
Whippany, NJ 07981 The Senior Manager Medical Device Safety (MDS) carries out global Pharmacovigilance (PV) business processes and analyses/trends safety data sets related to complaint handling ...
Whippany, NJ 07981 The Senior Manager Medical Device Safety (MDS) carries out global Pharmacovigilance (PV) business processes and analyses/trends safety data sets related to complaint handling ...
Whippany, NJ 07981 The Senior Manager Medical Device Safety (MDS) carries out global Pharmacovigilance (PV) business processes and analyses/trends safety data sets related to complaint handling ...
Medical Device Cybersecurity Analyst (On Site) Location: York, Pennsylvania Client: Healthcare domain Note: Need someone with a strong healthcare background who can work onsite 3days a week. Job ...
Medical Device Cybersecurity Analyst (On Site) Location: York, Pennsylvania Client: Healthcare domain Note: Need someone with a strong healthcare background who can work onsite 3days a week. Job ...
Job Title: Sr. Engineer, Combination Products & Medical Device Location: Columbus, OH Job Type ... Drives, as appropriate, key activities such as risk analysis, FMEA and threshold analysis for ...
Job Title: Sr. Engineer, Combination Products & Medical Device Location: Columbus, OH Job Type ... Drives, as appropriate, key activities such as risk analysis, FMEA and threshold analysis for ...
Job Title: Sr. Engineer, Combination Products & Medical Device Location: Columbus, OH Job Type ... Drives, as appropriate, key activities such as risk analysis, FMEA and threshold analysis for ...
Job Title: Sr. Engineer, Combination Products & Medical Device Location: Columbus, OH Job Type ... Drives, as appropriate, key activities such as risk analysis, FMEA and threshold analysis for ...
Madison, WI · On-site
$40 - $60/hr
Before lunch, you finalize a verification protocol and walk interns through the setup so execution ... Analytical mindset with strong problem-solving, organization, and communication skills. * Proven ...
New
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Madison, WI · On-site
$40 - $60/hr
Before lunch, you finalize a verification protocol and walk interns through the setup so execution ... Analytical mindset with strong problem-solving, organization, and communication skills. * Proven ...
New
Carmel, IN · On-site
$17.75 - $23.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
New
Carmel, IN · On-site
$17.75 - $23.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
New
Carmel, IN · On-site
$17.75 - $23.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
New
Carmel, IN · On-site
$17.75 - $23.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
New
$18 - $24/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
New
$18 - $24/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
New
$17.75 - $23.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
New
$17.75 - $23.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
New
$17.75 - $23.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
New
$17.75 - $23.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
New
$17.75 - $23.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
New
$17.75 - $23.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
New
Carmel, IN · On-site
$17.75 - $23.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
New
Carmel, IN · On-site
$17.75 - $23.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
New
$17.75 - $23.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
New
$17.75 - $23.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
New
Pomona, CA · On-site
$20/hr
... analysis and implement corrective actions under the guidance of Supervisor or Manager · ... preferable in medical device manufacturing · MS Office Suite experience · Knowledge of ...
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Pomona, CA · On-site
$20/hr
... analysis and implement corrective actions under the guidance of Supervisor or Manager · ... preferable in medical device manufacturing · MS Office Suite experience · Knowledge of ...
The DD&T US Medical Device Investigation Analyst is responsible for leading and documenting investigations related to Takeda developed & owned software and connected medical devices used in US PDT ...
The DD&T US Medical Device Investigation Analyst is responsible for leading and documenting investigations related to Takeda developed & owned software and connected medical devices used in US PDT ...
Bannockburn, IL · On-site
$89K - $141K/yr
The DD&T US Medical Device Investigation Analyst is responsible for leading and documenting investigations related to Takeda developed & owned software and connected medical devices used in US PDT ...
Bannockburn, IL · On-site
$89K - $141K/yr
The DD&T US Medical Device Investigation Analyst is responsible for leading and documenting investigations related to Takeda developed & owned software and connected medical devices used in US PDT ...
$89K - $141K/yr
The DD&T US Medical Device Investigation Analyst is responsible for leading and documenting investigations related to Takeda developed & owned software and connected medical devices used in US PDT ...
$89K - $141K/yr
The DD&T US Medical Device Investigation Analyst is responsible for leading and documenting investigations related to Takeda developed & owned software and connected medical devices used in US PDT ...
Milwaukee, WI · On-site
$84K - $114K/yr
We are a diverse and fast growing medical device & equipment company that is committed to focusing ... Develop, analyze, prioritize and execute in order to execute territory plans to achieve business ...
Quick apply
Milwaukee, WI · On-site
$84K - $114K/yr
We are a diverse and fast growing medical device & equipment company that is committed to focusing ... Develop, analyze, prioritize and execute in order to execute territory plans to achieve business ...
| Aspect | Internship Medical Device Analyst | Medical Device Quality Assurance Intern |
|---|---|---|
| Required Credentials | Typically pursuing or recent graduate in life sciences, engineering, or related fields | Similar educational background, often with coursework in quality systems or regulatory affairs |
| Work Environment | Hands-on analysis, data review, and supporting product development | Assisting in quality audits, documentation, and compliance activities |
| Employer & Industry Usage | Used in medical device companies focusing on product analysis and development | Common in companies emphasizing quality management and regulatory compliance |
The Internship Medical Device Analyst role focuses on analyzing medical devices, data review, and supporting product development, while the Medical Device Quality Assurance Intern concentrates on quality processes, audits, and compliance. Both roles are entry-level internships requiring similar educational backgrounds and are used within medical device companies but serve different functions within the industry.

$50/hr
Contractor
Medical, Dental, Vision, Life, Retirement, PTO
Posted 11 days ago
Job Title: Medical Device Engineer
Job Description
Support the development, validation, and optimization of electrochemical test methods used for next-generation medical monitoring technologies. Partner with engineers to execute validation activities, perform laboratory testing, analyze data, and generate technical documentation supporting test method development and equipment qualification efforts.
Responsibilities
Essential Skills
Additional Skills & Qualifications
Work Environment
R&D environment supporting product development and test method validation. Cross-functional collaboration with engineers, scientists, and technicians. Mix of laboratory testing, data analysis, technical writing, and validation activities. Standard business hours with hands-on laboratory work in a highly regulated medical device development setting.
Job Type & LocationThis is a Contract to Hire position based out of San Diego, CA.
Pay and BenefitsThe pay range for this position is $50.00 - $50.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)
This is a fully onsite position in San Diego,CA.
Application DeadlineThis position is anticipated to close on Jul 24, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.
Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.
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Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
5,001 - 10,000 Employees
Hanover, MD, US
1983