Support Design History File (DHF) activities for medical device development projects. * Review ... Collaborate with Design, Quality, Regulatory, Manufacturing, and Project Management teams to ...
Support Design History File (DHF) activities for medical device development projects. * Review ... Collaborate with Design, Quality, Regulatory, Manufacturing, and Project Management teams to ...
Medical Devices - R&D Project Manager Engineering Team
Barrington, IL · On-site
$90 - $140/hr
Project Manager Location: North Barrington, IL Employment Type: Full-Time About Us Founded in 1996, Medical Murray is a privately owned medical device company specializing in the development ...
Medical Devices - R&D Project Manager Engineering Team
Barrington, IL · On-site
$90 - $140/hr
Project Manager Location: North Barrington, IL Employment Type: Full-Time About Us Founded in 1996, Medical Murray is a privately owned medical device company specializing in the development ...
Project Manager, Senior Staff
Austin, TX · On-site
Confluent Medical Technologies is a financially healthy and rapidly growing medical device company ... Knowledge of project management basics including; scheduling building, tracking, management, and ...
Project Manager, Senior Staff
Austin, TX · On-site
Confluent Medical Technologies is a financially healthy and rapidly growing medical device company ... Knowledge of project management basics including; scheduling building, tracking, management, and ...
Medical Devices - R&D Project Manager Engineering Team
Barrington, IL · On-site
$90K - $140K/yr
Lead disposable medical device development projects from concept through production and ... Manage project scope, deliverables, and timelines to ensure successful project execution * Support ...
Quick apply
Medical Devices - R&D Project Manager Engineering Team
Barrington, IL · On-site
$90K - $140K/yr
Lead disposable medical device development projects from concept through production and ... Manage project scope, deliverables, and timelines to ensure successful project execution * Support ...
Project Manager
Rochester Hills, MI · On-site
Experience managing equipment projects for medical device, pharmaceutical, life sciences, or other regulated industries * Strong understanding of machine development, engineering processes, and ...
Quick apply
Project Manager
Rochester Hills, MI · On-site
Experience managing equipment projects for medical device, pharmaceutical, life sciences, or other regulated industries * Strong understanding of machine development, engineering processes, and ...
Senior Operations Project Manager - Medical Devices
Headquarters, ID · On-site
$90 - $120/hr
PROCEPT BioRobotics Corporation in Idaho is seeking an experienced Senior Project Manager, Operations, to lead innovative projects in medical device development. The role involves managing cross ...
New
Senior Operations Project Manager - Medical Devices
Headquarters, ID · On-site
$90 - $120/hr
PROCEPT BioRobotics Corporation in Idaho is seeking an experienced Senior Project Manager, Operations, to lead innovative projects in medical device development. The role involves managing cross ...
New
Job Title: Sr. Engineer, Combination Products & Medical Device Location: Columbus, OH Job Type ... Strong project management experience leading cross-functional teams. * Able to work independently ...
Job Title: Sr. Engineer, Combination Products & Medical Device Location: Columbus, OH Job Type ... Strong project management experience leading cross-functional teams. * Able to work independently ...
Job Title: Sr. Engineer, Combination Products & Medical Device Location: Columbus, OH Job Type ... Strong project management experience leading cross-functional teams. * Able to work independently ...
Job Title: Sr. Engineer, Combination Products & Medical Device Location: Columbus, OH Job Type ... Strong project management experience leading cross-functional teams. * Able to work independently ...
Minimum 10 years' experience in the medical device industry 5+ years of project management experience in the medical device industry. Proven track record of managing complex, multi-disciplinary ...
Minimum 10 years' experience in the medical device industry 5+ years of project management experience in the medical device industry. Proven track record of managing complex, multi-disciplinary ...
Project Manager, Staff - BAYP3035
Fremont, CA · On-site
$103K - $173K/yr
Prior experience scoping, planning, executing, and closing medical device projects. * Ability to define and manage scope across the product development life cycle. Establishment, organization ...
Project Manager, Staff - BAYP3035
Fremont, CA · On-site
$103K - $173K/yr
Prior experience scoping, planning, executing, and closing medical device projects. * Ability to define and manage scope across the product development life cycle. Establishment, organization ...
Project Manager MedTech / Medical Devices / SF Bay Representing a pioneering medical device company that specializes in the development of unique life-saving Medical Technologies. They are currently ...
Project Manager MedTech / Medical Devices / SF Bay Representing a pioneering medical device company that specializes in the development of unique life-saving Medical Technologies. They are currently ...
Engineering Project Manager Highridge Medical creates the world's most innovative spinal solutions ... Strong working knowledge of medical device product development, including design control, risk ...
Engineering Project Manager Highridge Medical creates the world's most innovative spinal solutions ... Strong working knowledge of medical device product development, including design control, risk ...
Position Summary: The Sr. Project Manager position is primarily responsible for managing and ... Lead and coordinate assigned medical device projects, including development activities and ...
Position Summary: The Sr. Project Manager position is primarily responsible for managing and ... Lead and coordinate assigned medical device projects, including development activities and ...
Project Manager
Minneapolis, MN · On-site
... relevant medical device industry regulations and standards. • Identify potential project risks ... Hiring Manager Exemption Type # of Hires Needed 1 Wage Amount
Project Manager
Minneapolis, MN · On-site
... relevant medical device industry regulations and standards. • Identify potential project risks ... Hiring Manager Exemption Type # of Hires Needed 1 Wage Amount
Medical Device Assembler I
$18.25 - $22.50/hr
The Medical Device Assembler I is responsible for performing a variety of production tasks related ... Other duties or projects as required Qualifications (Knowledge, Skills & Abilities): Minimum * High ...
Medical Device Assembler I
$18.25 - $22.50/hr
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Principal Scientist - Device Technical and Engineering Lead (Director Equivalent)
West Point, PA · On-site
$153.80 - $242.20/hr
... project teams. * Broad knowledge of medical device development, design controls and risk management, alongside deep knowledge in device design, requirement management, design verification, automation ...
Principal Scientist - Device Technical and Engineering Lead (Director Equivalent)
West Point, PA · On-site
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... project teams. * Broad knowledge of medical device development, design controls and risk management, alongside deep knowledge in device design, requirement management, design verification, automation ...
Clinical Engineering Medical Device Network Engineer II
Corning, IA · On-site
$45.04 - $67/hr
Every day you will collaborate with the CE Medical Device Security Team on remediation solutions, guide other technicians on complex medical device projects, and manage vendor-related vulnerabilities.
Clinical Engineering Medical Device Network Engineer II
Corning, IA · On-site
$45.04 - $67/hr
Every day you will collaborate with the CE Medical Device Security Team on remediation solutions, guide other technicians on complex medical device projects, and manage vendor-related vulnerabilities.
Our F500 Medical Device client has an exciting opportunity for a Sr. Project Manager. Job Summary: Responsible for implementing and supporting project management processes. Candidate will establish ...
Our F500 Medical Device client has an exciting opportunity for a Sr. Project Manager. Job Summary: Responsible for implementing and supporting project management processes. Candidate will establish ...
Sr. Project Manager
Brooklyn Park, MN · On-site
Position Summary: The Sr. Project Manager position is primarily responsible for managing and ... Lead and coordinate assigned medical device projects, including development activities and ...
Sr. Project Manager
Brooklyn Park, MN · On-site
Position Summary: The Sr. Project Manager position is primarily responsible for managing and ... Lead and coordinate assigned medical device projects, including development activities and ...
... medical device, pharmaceutical, biotechnology, or related regulated industries. * Strong understanding of project management principles, including scope management, scheduling, budgeting, resource ...
... medical device, pharmaceutical, biotechnology, or related regulated industries. * Strong understanding of project management principles, including scope management, scheduling, budgeting, resource ...
Seasonal Medical Device Project Manager information
See salary details
$25.24 - $29.44
3% of jobs
$29.44 - $33.63
1% of jobs
$33.63 - $37.83
0% of jobs
$37.83 - $42.02
20% of jobs
$42.20 is the 25th percentile. Wages below this are outliers.
$42.02 - $46.22
19% of jobs
The median wage is $48.95 / hr.
$46.22 - $50.42
11% of jobs
$50.42 - $54.61
3% of jobs
$54.61 - $58.81
4% of jobs
$58.81 - $63
11% of jobs
$64.24 is the 75th percentile. Wages above this are outliers.
$63 - $67.20
12% of jobs
$67.20 - $71.39
17% of jobs
$25
$53
$71
How much do seasonal medical device project manager jobs pay per hour?
What is the difference between Seasonal Medical Device Project Manager vs Medical Device Quality Assurance Specialist?
| Aspect | Seasonal Medical Device Project Manager | Medical Device Quality Assurance Specialist |
|---|---|---|
| Credentials | Project management certification (PMP), relevant industry experience | ISO 13485 training, quality assurance certifications |
| Work Environment | Project teams, manufacturing sites, regulatory agencies | Quality departments, laboratories, compliance offices |
| Employer & Industry Usage | Medical device companies during peak seasons or product launches | Manufacturers ensuring product quality and regulatory compliance |
| Search & Comparison Intent | Understanding project management roles in medical device industry | Quality assurance roles and compliance responsibilities |
The Seasonal Medical Device Project Manager focuses on managing projects during specific seasons or product launches, coordinating teams, and ensuring timely delivery. In contrast, the Medical Device Quality Assurance Specialist concentrates on maintaining product quality, compliance with regulations, and conducting audits. Both roles require industry-specific certifications and work within the medical device manufacturing environment, but their core responsibilities differ significantly.
What cities are hiring for Seasonal Medical Device Project Manager jobs?
Cities with the most Seasonal Medical Device Project Manager job openings:
What states have the most Seasonal Medical Device Project Manager jobs?
States with the most job openings for Seasonal Medical Device Project Manager jobs include:
What job categories do people searching Seasonal Medical Device Project Manager jobs look for?
The top searched job categories for Seasonal Medical Device Project Manager jobs are:
- Renovia
- Before And After School Internal Project Manager
- Performance Improvement Project Manager
- Full Time Wireless Project Manager
- Work From Home Project Manager
- International Project Construction Manager
- Wireless Project Manager
- No Experience Project Management
- Work From Home Project Management
- Project Manager Project Manager

Full-time
Posted 24 days ago
Job description
This role focuses on supporting Design History File (DHF) activities for medical device development projects, ensuring compliance with regulatory and quality system requirements. The engineer will be responsible for managing risk documentation, product specifications, and design control processes throughout the product lifecycle.
Key Responsibilities:
- Support Design History File (DHF) activities for medical device development projects.
- Review, update, and maintain Global dFMEA documentation, ensuring risks are adequately identified, analyzed, and mitigated.
- Review, update, and maintain Global uFMEA documentation based on product use scenarios and user-related risks.
- Develop and update Preliminary Hazard Analysis (PHA) documentation in accordance with risk management procedures.
- Support creation and maintenance of product risk management files throughout the development lifecycle.
- Prepare, review, and update Product Characterization documents to define product performance and design intent.
- Create and maintain Product Specification Documents (PSD) ensuring alignment with design requirements and customer needs.
- Develop and update Critical-to-Quality (CTQ) documents and establish measurable quality requirements.
- Support development and maintenance of Design Input, Design Output, Verification, and Validation documentation.
- Ensure traceability between user needs, design inputs, risk controls, verification activities, and design outputs.
- Collaborate with Design, Quality, Regulatory, Manufacturing, and Project Management teams to support product development deliverables.
- Participate in design reviews and provide technical input on risk management and DHF compliance.
- Support engineering change assessments and associated documentation updates.
- Review engineering documents for completeness, accuracy, and compliance with quality system requirements.
- Identify gaps in documentation and recommend corrective actions.
- Support audits, inspections, and compliance activities related to design control and risk management documentation.
- Contribute to continuous improvement initiatives for product development and design control processes.
- Ensure all deliverables comply with applicable regulatory, quality, and Zimmer Biomet procedures and standards.
Required Skills:
- Ability to establish document traceability between User Needs, Design Inputs, Design Outputs, Risk Management, Verification, and Validation records within Cockpit Cognition.
- Experience supporting DHF gap assessments, document linking, metadata management, and compliance reviews.
- Familiarity with digital DHF structure, document hierarchy, and traceability matrix development.
- Knowledge of DHF remediation projects and legacy design documentation migration into Cockpit Cognition.
- Strong written and verbal communication skills to convey direction and project plans with appropriate personnel from other departments.
About Prophecy Consulting
Sourced by ZipRecruiter
Company size
11 - 50 Employees
Headquarters location
Irvine, CA, US
Year founded
2018