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Medical Device Program Manager Jobs in Mansfield, MA

SharkNinja

QMS Program Manager

Needham, MA · On-site

QMS Program Manager, Medical Devices Needham, MA, United States As the QMS Program Manager, Medical ... Working knowledge of medical device quality requirements, including ISO 13485, ISO 14971, FDA 21 ...

Henderson Scott Limited

Program Manager

Boston, MA · On-site

Device & Asset Lifecycle Management - standardizing device fleets, improving inventory/asset ... Multi-Site Program & Budget Planning - sequencing and financing phased rollouts across many ...

Philips

Program Manager (Sustaining)

Cambridge, MA

$136K - $216K/yr

Owning the sustainment program management for a portfolio of medical devices, including hardware, Software as a Medical Device (SaMD), and connected digital platforms. Ensuring products in the field ...

JRG Partners

Marketing Program Manager

Boston, MA · On-site

Marketing Programs Manager Status: Exempt Position: Reports to: Vice President, Marketing Our ... At least 5 years of experience in medical device or pharma companies * Skills: * Very comfortable ...

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All JobsMedical Device Program JobsMedical Device Program Manager JobsMedical Device Program Manager Jobs in Mansfield, MA

Medical Device Program Manager information

See Mansfield, MA salary details

$40.8K

$113.8K

$166.2K

How much do medical device program manager jobs pay per year?

As of Aug 12, 2026, the average yearly pay for medical device program manager in Mansfield, MA is $113,758.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,200.00 and $140,300.00 per year, depending on experience, location, and employer.

What is the difference between Medical Device Program Manager vs Medical Device Quality Engineer?

AspectMedical Device Program ManagerMedical Device Quality Engineer
CredentialsProject management certifications, engineering degreeQuality assurance certifications (e.g., CQE), engineering degree
Work EnvironmentCross-functional teams, project planning, product developmentQuality systems, compliance, testing, and validation
Employer & Industry UsageMedical device companies, manufacturing, R&DRegulatory agencies, manufacturing, quality departments
Search & Comparison IntentManaging projects, product launches, timelinesEnsuring quality, compliance, risk management

The Medical Device Program Manager focuses on overseeing product development projects, coordinating teams, and ensuring timely delivery. In contrast, the Medical Device Quality Engineer concentrates on maintaining quality standards, regulatory compliance, and testing processes. Both roles are essential in the medical device industry but serve different functions within the product lifecycle.

What are the key skills and qualifications needed to thrive as a medical device program manager, and why are they important?

To thrive as a Medical Device Program Manager, you need a strong background in project management, regulatory compliance, and biomedical engineering or a related field, often supported by a relevant degree and industry experience. Familiarity with project management tools (such as MS Project), quality management systems (QMS), and certifications like PMP or Six Sigma are highly valued. Exceptional leadership, cross-functional communication, and problem-solving skills help drive successful product development and team coordination. These competencies ensure programs meet regulatory standards, stay on schedule, and deliver safe, effective medical devices to market.

What is a medical device program manager?

A Medical Device Program Manager oversees the planning, development, and execution of projects related to medical devices within a company. They coordinate cross-functional teams, manage timelines, ensure regulatory compliance, and serve as the main point of contact for stakeholders. Their role is crucial in bringing safe and effective medical devices from concept to market, ensuring that all aspects of the program meet quality and regulatory standards. Medical Device Program Managers often work closely with engineering, quality assurance, regulatory affairs, and marketing teams.

How does a medical device program manager typically collaborate with cross-functional teams during product development?

A Medical Device Program Manager works closely with cross-functional teams including engineering, regulatory affairs, quality assurance, manufacturing, and marketing throughout the product development lifecycle. They coordinate timelines, facilitate communication, and resolve conflicts to ensure project milestones are met while maintaining compliance with regulatory standards. Regular meetings and progress updates are essential, as the Program Manager acts as a central point of contact to align various team goals and address issues proactively. This collaborative approach helps streamline development and supports successful product launches.
What job categories do people searching Medical Device Program Manager jobs in Mansfield, MA look for? The top searched job categories for Medical Device Program Manager jobs in Mansfield, MA are:
What cities near Mansfield, MA are hiring for Medical Device Program Manager jobs? Cities near Mansfield, MA with the most Medical Device Program Manager job openings:
Medical Device Program Manager jobs near you

Senior Mechanical Engineer - Medical Device

Micro Leads Inc

Somerville, MA • On-site

$80K - $100K/yr

Full-time

Medical, Dental, Life

Re-posted 14 days ago

Job description

Location: Somerville, MA

Senior Mechanical Engineer – Medical Device

Overview:

Micro-Leads is a fast-paced early-stage company developing an injectable medical device to treat people with chronic pain with greater efficacy. Our company has extensive expertise in precision implantable medical devices for nerve stimulation and neuromodulation.

Role Summary:

The primary role of this position is to design and build injectable electrodes for needle delivery and implantable pulse generator housings for next-generation neurostimulator devices. The individual will design electrodes for stimulation and nerve recordings.  In addition, the candidate will prototype, build, and conduct mechanical integrity and related tests. The individual will also develop manufacturing processes and work with vendors to manufacture components.

The candidate must have significant background in medical device development, implantable electrodes, process development, and verification and validation. The individual should be hands-on and have direct experience working with vendors and design transfer to contract manufacturers.

Responsibilities:

  • Mechanical design of implantable electrodes for neuromodulation 
  • End-to-end development of assembly and manufacturing processes
  • Design of processes for thin substrate laminations and bonding techniques
  • Design of microscale assembly techniques, including scaling to manufacturability
  • Develop micro-molding, thermoforming, and lamination methods for thin substrates and catheters
  • Create 3D assemblies and technical drawings of electrodes and implantable housings using SolidWorks and AutoCAD
  • Identify, source, and manage vendors to obtain hardware components on a schedule (e.g. procuring materials, services from machine shops or 3D printing houses, contract manufacturing)
  • Develop mechanical testing structures and set up accelerated lifetime tests
  • Manage engineering personnel as necessary (e.g. junior engineers, technicians, co-ops)
  • Adhere to Micro-Leads quality management system, understands essential regulatory requirements, and follows standard operating procedures
  • Maintain design control requirements related Micro-Leads’ QMS including developing design inputs/outputs, risk management, verification and validation

Minimum qualifications:

  • B.S. in Mechanical or Biomedical Engineering, M.S. Preferred
  • 2-4 years of related professional experience post-Bachelor’s Degree

Desired qualifications & experience:

  • Successful candidates must be able to multi-task and work effectively as part of a small team
  • Successful candidates will have excellent benchtop capability including the dexterity to manipulate small structures under a stereomicroscope
  • Familiarity with standard tooling for rapid prototyping (e.g. drill presses, saws, welding, soldering, CNC mills)
  • Experience with precision microscale assembly of silicone electrodes using processes such as injection molding, casting, micro-fluidic molding, etc.
  • Experience with Class III implantable systems and hermetic manufacturing methods
  • Experience with precision microscale assembly of silicone electrodes using processes such as injection molding, thermoforming, lamination, micro-molding, etc.

Benefits:

  • Medical Insurance
  • Dental Insurance
  • Vision Insurance
  • Stock Options

Company Description

Micro-Leads is a fast-paced early-stage company developing an injectable medical device to treat people with chronic pain with greater efficacy. Our company has extensive expertise in precision implantable medical devices for nerve stimulation and neuromodulation.