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Seasonal Medical Device Project Manager Jobs (NOW HIRING)

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 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 ...

... 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

Eden Prairie, MN

$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 ...

Showing results 41-60

Seasonal Medical Device Project Manager information

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$25

$53

$71

How much do seasonal medical device project manager jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for seasonal medical device project manager in the United States is $53.24, according to ZipRecruiter salary data. Most workers in this role earn between $41.35 and $65.62 per hour, depending on experience, location, and employer.

What is the difference between Seasonal Medical Device Project Manager vs Medical Device Quality Assurance Specialist?

AspectSeasonal Medical Device Project ManagerMedical Device Quality Assurance Specialist
CredentialsProject management certification (PMP), relevant industry experienceISO 13485 training, quality assurance certifications
Work EnvironmentProject teams, manufacturing sites, regulatory agenciesQuality departments, laboratories, compliance offices
Employer & Industry UsageMedical device companies during peak seasons or product launchesManufacturers ensuring product quality and regulatory compliance
Search & Comparison IntentUnderstanding project management roles in medical device industryQuality 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.

More about Seasonal Medical Device Project Manager jobs

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:

Infographic showing various Seasonal Medical Device Project Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, and 7% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $110,731 per year, or $53.2 per hour.

Medical Device DHF Engineer

Prophecy Technologies

Indianapolis, IN • On-site

Full-time

Posted 24 days ago


Job description

Role Overview:
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.