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Internship Product Manager Medical Device Jobs (NOW HIRING)

Vitrolife Group

... Medical Device & Equipment Account Manager to join our North American Sales Team. This role is ... Conduct routine customer visits, product demonstrations, in-services, and procedural observations.

VOLT

Medical Device Assembler

Plymouth, MN · On-site

$17.50 - $19.25/hr

Experience as a Medical Device Assembler or Production Assembler. * Strong attention to detail ... quality, and compliance standards * Ability to follow written work instructions and SOPs.

Adecco

Medical Device Assembler

Dublin, OH · On-site

$16/hr

Visual inspection of product to ensure good quality using various types of magnification ... For instant consideration for this Medical Device Assembler position with Adecco in Dublin, OH ...

Marquee Staffing - OC

Be Seen First

Medical Device Packaging (Cleanroom)

Lake Forest, CA · On-site

$20 - $21/hr

Assemble, inspect, and package medical device products according to specifications and procedures. * Follow SOPs, work instructions, engineering drawings, and inspection procedures. * Maintain ...

New

Astrix Inc

Medical Device Assembler

Santa Rosa, CA · On-site

$22 - $24/hr

Pay Rate Low: 22 | Pay Rate High: 24 A medical device manufacturer is seeking a Production/Assembly Technician to build high-quality medical devices in accordance with approved manufacturing process ...

VOLT

Medical Device Assembler

Irvine, CA · On-site

$18 - $19.75/hr

Accurately complete paper and electronic documentation to maintain full product traceability and ... Prior experience as a Medical Device Assembler or Production Assembler preferred. * Previous ...

Bracco

Medical Device Assembler I

Eden Prairie, MN · On-site

$18.25 - $22.50/hr

The Medical Device Assembler I is responsible for performing a variety of production tasks related to the assembly and testing of electro-mechanical medical devices. Utilizing established work ...

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Internship Product Manager Medical Device information

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$916

$2K

How much do internship product manager medical device jobs pay per month?

As of Aug 23, 2026, the average monthly pay for internship product manager medical device in the United States is $2,000.00, according to ZipRecruiter salary data. Most workers in this role earn between $2,000.00 and $2,000.00 per month, depending on experience, location, and employer.

What is the difference between Internship Product Manager Medical Device vs Product Coordinator Medical Device?

AspectInternship Product Manager Medical DeviceProduct Coordinator Medical Device
Required CredentialsTypically pursuing or recent graduate in related fieldRelevant experience or certification often preferred
Work EnvironmentInternship setting within medical device companies, collaborative teamsOperational support in product management teams, cross-functional roles
Employer & Industry UsageCommon in medical device firms, entry-level roleUsed in medical device companies, supporting product lifecycle

The Internship Product Manager Medical Device is an entry-level role focused on learning and supporting product management tasks, often filled by students or recent graduates. In contrast, the Product Coordinator Medical Device handles more operational responsibilities within product teams, requiring some experience. Both roles are integral to medical device companies but differ mainly in experience level and scope of responsibilities.

How to become an internship product manager in medical device?

To become an internship product manager in the medical device industry, candidates typically need a bachelor's degree in fields like engineering, business, or healthcare, along with strong communication and project management skills. Relevant experience through coursework, internships, or certifications such as Agile or Lean can be beneficial. Familiarity with medical device regulations and tools like product lifecycle management software also enhances prospects.

How to become an internship product manager medical device?

To become an internship product manager in the medical device industry, candidates typically need a bachelor's degree in engineering, business, or a related field, along with strong communication and project management skills. Relevant experience through coursework, internships, or certifications in healthcare or medical devices can enhance prospects. Familiarity with product lifecycle management tools and understanding regulatory standards like FDA requirements are also beneficial.
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Internship Product Manager Medical Device jobs near you
Infographic showing various Internship Product Manager Medical Device 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 $24,000 per year, or $11.5 per hour.

Quality Manager - Medical Device/ ISO 13485

Vonco Products LLC

Trevor, WI • On-site

Full-time

Posted 8 days ago

Job description

Job Type
Full-time
Description
Quality Manager ISO 13485 Medical Device Manufacturing
We are seeking a hands-on Quality Manager who can lead and continuously improve our ISO 13485 Quality Management System while supporting a fast-paced medical device packaging manufacturing operation. This individual will serve as the site quality leader, partnering closely with Operations, Engineering, Supply Chain, and Customer Service to ensure compliance, drive continuous improvement, and maintain customer confidence.
The ideal candidate is a proactive quality leader with experience in medical devices, healthcare packaging, or other regulated manufacturing environments. They are comfortable balancing strategic quality system oversight with day-to-day operational support and can effectively influence cross-functional teams.
Basic Purpose and Function: The Quality Manager is responsible for developing, implementing, maintaining, and continuously improving the organization's Quality Management System (QMS) in accordance with ISO 13485, applicable regulatory requirements, customer requirements, and company objectives.
This position serves as the site's management representative for the Quality Management System. It ensures that product realization activities, risk management processes, supplier controls, CAPA activities, and post-market quality processes effectively support the manufacture of safe and effective medical devices.
The Quality Manager partners closely with Operations, Engineering, Supply Chain, and Customer Service teams to ensure compliance while driving a culture of quality and continuous improvement.
Job Responsibilities:
Quality Management System (QMS)
  • Manage and maintain the ISO 13485 Quality Management System.
  • Ensure compliance with all applicable regulatory and customer requirements.
  • Oversee document control and record retention processes.
  • Coordinate Management Review activities and present quality system performance metrics.
  • Ensure quality objectives are established, monitored, and achieved.
  • Maintain inspection readiness and audit preparedness.

CAPA and Nonconformance Management
  • Lead the Corrective and Preventive Action (CAPA) program.
  • Ensure timely investigation and closure of quality issues.
  • Facilitate root cause investigations.
  • Monitor effectiveness of corrective actions.
  • Manage nonconforming product processes and disposition activities.

Risk Management
  • Ensure risk management activities comply with ISO 14971 requirements.
  • Participate in risk assessments associated with products, processes, equipment, and suppliers.
  • Support implementation of risk controls and verification of effectiveness.
  • Ensure risk management files remain current and complete.

Validation and Quality Engineering Support
  • Review and approve validation protocols and reports.
  • Support process improvement and process capability initiatives.
  • Ensure manufacturing changes are properly evaluated and validated.

Internal Audits and Regulatory Inspections
  • Manage the internal audit program.
  • Coordinate external audits, customer audits, certification audits, and regulatory inspections.
  • Track audit findings through closure.

Supplier Quality Management
  • Ensure supplier qualifications and monitoring programs meet ISO 13485 requirements.
  • Manage supplier audits and supplier performance reviews.
  • Oversee supplier corrective action requests (SCARs).
  • Support supplier risk assessments and change management.

Customer Quality and Complaint Handling
  • Manage customer complaint investigations.
  • Ensure complaint-handling processes meet applicable regulatory requirements.
  • Analyze customer quality trends and implement improvement actions.
  • Serve as primary escalation point for customer quality issues.

Training and Quality Culture
  • Ensure employee training programs meet regulatory and quality requirements.
  • Verify personnel competency for quality-critical tasks.
  • Promote quality awareness throughout the organization.
  • Support continuous improvement initiatives across all departments.

Leadership Responsibilities
  • Lead and develop Quality Specialists, Technicians, Auditors, and Inspectors.
  • Establish departmental goals and objectives.
  • Manage department resources.
  • Provide quality guidance to Operations, Engineering, and Customer Service.

Success Measures
  • Successful maintenance of ISO 13485 certification
  • Timely closure and effectiveness of CAPAs
  • Reduction in customer complaints and internal quality issues
  • Successful completion of internal, customer, and certification audits
  • Supplier quality performance improvements
  • On-time completion of Management Reviews and Quality Objectives

Requirements
Required Background
  • Bachelor's degree in engineering, Quality, Manufacturing, Life Sciences, or related field.
  • 5+ years of progressive quality experience in a regulated manufacturing environment.
  • 3+ years working with ISO 13485 Quality Management Systems.
  • Experience leading internal, customer, and certification audits.
  • Strong knowledge of CAPA, nonconformance management, change control, complaint handling, and supplier quality.
  • Experience in FDA-regulated manufacturing is highly preferred.

Key Characteristics
  • Strong leadership presence with the ability to coach and develop quality personnel.
  • Highly organized and detail-oriented.
  • Effective communicator who can build credibility across all levels of the organization.
  • Skilled problem solver with root cause analysis experience.
  • Comfortable making risk-based decisions in a regulated environment.
  • Able to balance compliance requirements with operational realities.

Technical Expertise: demonstrated experience with:
  • ISO 13485
  • CAPA systems
  • Internal auditing
  • Risk management (ISO 14971 preferred)
  • Supplier qualification and supplier corrective actions
  • Validation activities (IQ/OQ/PQ)
  • Complaint investigations
  • Document control and change management

Physical Requirements
• Reaching, standing, walking, pushing, pulling, lifting, typing, grasping, feeling, talking, hearing, seeing, and repetitive motions.
• This position frequently requires the use of hands to handle or feel objects, tools, or controls, and to reach with hands and arms.
• The associate must occasionally lift and/or move up to 40 pounds. Specific vision abilities required by this job include close vision and the ability to adjust focus.

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