ZipRecruiter

Log In

1

Medical Device Program Manager Jobs in Missouri (NOW HIRING)

kindeva

Senior Device Engineer

Maryland Heights, MO

$101K - $138K/yr

... Medical Device Directives * Understanding of production and production systems in a GMP regulated environment * Strong technical project management, critical thinking, and problem-solving skills.

kindeva

Senior Device Engineer

Maryland Heights, MO

$101K - $138K/yr

... Medical Device Directives * Understanding of production and production systems in a GMP regulated environment * Strong technical project management, critical thinking, and problem-solving skills.

kindeva

Senior Device Engineer

Maryland Heights, MO · On-site

$101K - $138K/yr

... Medical Device Directives * Understanding of production and production systems in a GMP regulated environment * Strong technical project management, critical thinking, and problem-solving skills.

TalentBurst, Inc.

Program Manager

Saint Joseph, MO

Program Manager St. Joseph Missouri 64506 24 Months Duties: Shift: 1st shift Hours: minimum 45 ... We offer competitive compensation and comprehensive benefits, including medical, dental, vision ...

ProPharma Group

... device programs. Do you have a degree in Life Science, Nursing or Medicine, paired with a true ... management training, industry training and the opportunity to learn from the wider MI Team by ...

REDISCOVER

Licensed Program Manager

Kansas City, MO

... medical record. Requirements of the Position * Master's degree in a social science field as defined ... Program Manager through training, collaboration, and meaningful work. Ready to join a team that ...

REDISCOVER

Licensed Program Manager

Kansas City, MO · On-site

... medical record. Requirements of the Position * Master's degree in a social science field as defined ... Program Manager through training, collaboration, and meaningful work. Ready to join a team that ...

BJC HealthCare

Program Manager - Psychology

Saint Louis, MO · On-site

$92K - $150K/yr

Additional Information About the Role Program Manager - Psychology at St Louis Children's Hospital ... Partner with medical and hospital leadership to deliver integrated, patient-centered care * Expand ...

next page

Showing results 1-20

All JobsMedical Device Program JobsMedical Device Program Manager JobsMedical Device Program Manager Jobs in Missouri

Medical Device Program Manager information

See Missouri salary details

$36.1K

$100.8K

$147.3K

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

As of Jul 14, 2026, the average yearly pay for medical device program manager in Missouri is $100,798.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,600.00 and $124,300.00 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 are popular job titles related to Medical Device Program Manager jobs in Missouri? For Medical Device Program Manager jobs in Missouri, the most frequently searched job titles are:
What job categories do people searching Medical Device Program Manager jobs in Missouri look for? The top searched job categories for Medical Device Program Manager jobs in Missouri are:
What cities in Missouri are hiring for Medical Device Program Manager jobs? Cities in Missouri with the most Medical Device Program Manager job openings:
Medical Device Program Manager jobs near you
Infographic showing various Medical Device Program Manager job openings in Missouri as of July 2026, with employment types broken down into 74% Full Time, 18% Part Time, and 8% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $100,798 per year, or $48.5 per hour.
Senior Device Engineer

Senior Device Engineer

Kindeva Drug Delivery

Maryland Heights, MO • On-site

$101K - $138K/yr

Full-time

Re-posted 27 days ago

Job description

Our Work Matters
At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.
The Impact You Will Make
Works as a device engineering team lead or member/lead of cross-functional teams, as well as independent contributor throughout the Combination Product Life Cycle process. Leads or participates in cross-functional teams for design changes, design transfer activities, continuous improvement projects, investigations, risk assessments and protocol execution. Responsible for device life cycle management of on-market combination products and implementation of new products. Develops Design History File documents, Risk Management documents, change management technical impact assessments, test plans/ protocols, test method validations, and data analysis. Leads design changes from initiation through design transfer. Performs or oversees engineering, design, and development work. Develops design concepts/ideas for product improvements, fixtures, gages, and test methods. Develops prototypes of design concepts for engineering testing and evaluation. Generates or reviews/approves SOPs, test protocols, engineering test reports and provides laboratory oversight as needed. Responsible for adhering to design controls and documenting all product development work and updates in a Design History File.
Role Responsibilities
  • Leads or participates in design control, change management and risk management activities related to the combination device, design and manufacturing process ensuring compliance to all applicable regulations including FDA Regulation and Guidance for Combination Products
  • Perform Quality Risk Assessments
  • Performs or oversees biomedical/mechanical engineering design and development work, including design changes and product improvements, Geometric Design and Tolerancing, drawings, tolerance stacks, risk analyses, and engineering analyses. Establishes or reviews/approves specifications and inspection requirements for components, products, and processes.
  • Develops prototypes of design concepts for engineering testing and evaluation
  • Creates or reviews/ approves SOPs, Job Aids, test protocols, reports and risk-based plans for verification and validation testing.
  • Develops/ approves/ maintains DHF documents and rationales in support of design changes, design transfer, investigations, information requests, and product life cycle
  • Supports Manufacturing, QCD Lab, QDS Lab, Quality Engineering, and Quality Assurance with investigations and the qualification of new material/ processes/ equipment to assure reliability requirements are met. Participates in or leads CAPA investigations.
  • Provides input and technical support for device changes, document updates, process changes, risk management. Performs assessments for change control and may represent group and product on change control review committee. Accountable for change management projects or investigation actions related to the device, design, manufacturing process, or new/updated standards and regulations.
  • Develops test methods, fixtures, gages, challenge samples, limit samples, simulation devices, and engineering prototypes of design concepts
  • Develops or collaborates on and adheres to project plans, timelines, and budgets
  • Liaison with internal production sites, quality, regulatory R&D, and Tech Transfer/Launch Teams
  • Establish and maintain relationships with production sites and key stakeholders
  • Technical oversight of other engineers
  • May require management of cross-functional teams and indirect reports
  • Reports and escalates to leadership as appropriate
  • May provide training for new hires or contractors and may oversee work conducted by contractors or lab technicians.
  • Other duties as assigned

Basic Qualifications
  • Experience in Medical Device or Combination Products Design Controls, Production, Sustaining Engineering role or related field
  • B.S. Degree in Engineering discipline with 7 - 9 years experience
  • M.S. Degree in Engineering discipline with 5 - 7 years experience
  • Ph.D. in Engineering discipline with 3 - 5 years experience
  • (Biomedical Engineering or Mechanical Engineering preferred)

Preferred Qualifications
  • Thorough understanding and in-depth knowledge of FDA Design Control Regulations for Combination Products per 21 CFR Part 4 and/or Medical Devices per 21 CFR 820.30, ISO 13485 and ISO 14971 and related standards, and EU Medical Device Directives
  • Understanding of production and production systems in a GMP regulated environment
  • Strong technical project management, critical thinking, and problem-solving skills. Proficient in Smartsheet or MS Project.
  • Experience analyzing complex issues for patient/user impact
  • Understanding of Human factors and usability engineering
  • Conceptual design skills and experience with a variety of manufacturing methods (e.g. injection molding, machining, etc.)
  • Proficiency in SolidWorks design software, Mathcad, MindManager, and other general computer software such as word processing, spreadsheets, presentations, flow charts, etc. Strong laboratory skills such as component inspection or failure analysis, mechanical testing, etc. with a good understanding of GMP documentation and data integrity requirements.
  • Strong mathematical, analytical, and reasoning skills
  • Strong innovation skills and creativity astuteness
  • Strong teamwork and organizational skills
  • Strong written and oral communication
  • Knowledge of Design for Reliability and Manufacturing (DRM) and robust device design practices
  • Ability to prioritize multiple responsibilities and to work on multiple complex technical projects simultaneously
  • Experience with FDA investigators and other global regulatory agencies in the front room or providing back room support

#LI-onsite #LI-BM1
#LI-onsite #LI-BM1
California residents should review our Notice for California Employees and Applicants before applying.
Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees-regardless of format-without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.
Equal Opportunity Employer:
Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.
Do you see yourself as part of the Kindeva mission? Click Apply Now Today!

Apply