Program Manager - Contractor

Posted One Month Ago
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Olathe, KS, USA
In-Office
Expert/Leader
Healthtech • Pharmaceutical • Manufacturing
The Role
Provides program management consulting for complex medical technology projects, developing strategies, governance, implementation plans, risk mitigations, stakeholder communications, and data-driven recommendations. Coordinates cross-functional activities across initiation, planning, execution, verification, and design transfer while supporting product development, quality systems, regulatory requirements, and process improvements.
Summary Generated by Built In
Job Title: Program Manager (Independent Contractor)
Duration: 6-12-months (possibility of extension)
Employment Type: Independent Contractor (1099)
Department: Hardware, Technical Services
Point of Contact: Engineering Manager/Director
Location: Olathe, KS

Vantage MedTech provides comprehensive design and manufacturing services, supporting the advancement of medical technologies from concept through to product realization. We develop and manufacture new products for the treatment of heart failure, cancer, stroke, Gene Therapy, COPD, TBI, Atrial Fibrillation, Blood Clots, Brain Surgery, and many more! We are searching for top-tier talent to apply their gifts to making life better for hundreds of thousands of patients worldwide. If this is something you aspire to, we would like to talk with you!  
*This engagement is for an independent contractor (1099) providing services to Vantage MedTech for an anticipated period of 6-12 months, with potential for extension based on business needs. Contractors are not employees of Vantage MedTech and are not eligible for company-sponsored benefits.
Services:
Contractor shall provide Vantage with Program Management consulting services to support the successful planning, execution, and delivery of complex projects and programs. 

Scope: 
  • Developing and facilitating the execution of program strategies, governance structures, and implementation plans to achieve defined project objectives, timelines, budgets, and quality requirements.

  • Facilitating cross-functional collaboration and coordinating project activities through all phases of the program lifecycle, including initiation, planning, execution, verification, and design transfer, as applicable.

  • Identifying and evaluating program risks, issues, dependencies, and potential impacts, and providing recommendations and mitigation strategies to support successful project outcomes.

  • Serving as a strategic advisor to company stakeholders and customers by providing project status updates, insights, recommendations, and guidance throughout the engagement.

  • Facilitating meetings, workshops, and decision-making processes to align stakeholders, address challenges, and support project execution.

  • Providing data-driven analysis, reporting, and recommendations to support informed business decisions and achievement of program objectives.

  • Recommending process improvements, best practices, and operational efficiencies to enhance project performance and execution effectiveness.


Qualifications and Experience:
  • Bachelor's degree in engineering or a related technical discipline, or equivalent relevant experience.
  • Demonstrated expertise gained through 10+ years of providing program management, product development, engineering, or technical consulting services for complex projects and initiatives.

  • Experience supporting programs within medical device, healthcare technology, life sciences, or other regulated industries, with knowledge of applicable quality and regulatory requirements.

  • Proven ability to successfully deliver complex projects involving multiple stakeholders, third-party partners, and executive-level engagement.

  • Strong working knowledge of product development processes, design controls, quality systems, regulatory requirements, commercialization activities, and related industry best practices.

  • Demonstrated ability to provide strategic guidance, risk assessment, stakeholder facilitation, and project execution support in complex technical environments.

Vantage MedTech is committed to providing equal opportunity in the selection of contractors and service providers. We do not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status, or any other characteristic protected by applicable law. Contractor selection decisions are based on qualifications, expertise, experience, and business needs. All contractors must be authorized to perform services in the United States without sponsorship. For more information, visit www.vantagemedtech.com.
 

Skills Required

  • Bachelor's degree in engineering or a related technical discipline, or equivalent relevant experience
  • 10+ years of program management, product development, engineering, or technical consulting experience supporting complex projects and initiatives
  • Experience supporting programs within medical device, healthcare technology, life sciences, or other regulated industries
  • Knowledge of applicable quality and regulatory requirements
  • Experience delivering complex projects involving multiple stakeholders, third-party partners, and executive-level engagement
  • Strong working knowledge of product development processes, design controls, quality systems, regulatory requirements, commercialization activities, and related industry best practices
  • Ability to provide strategic guidance, risk assessment, stakeholder facilitation, and project execution support in complex technical environments
  • Authorization to perform services in the United States without sponsorship
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The Company
HQ: Moonachie, NJ
171 Employees
Year Founded: 1994

What We Do

Vantage MedTech provides comprehensive design and manufacturing services, supporting the advancement of medical technologies from concept through to product realization. Partnering with the world’s most innovative MedTech start-ups and large medical device companies, we offer feasibility support, product development and prototyping, new product development, clinical and commercial manufacturing, and after-market services to support every phase of the product life cycle. Our clients can leverage our proprietary Advantage Platforms™, accelerating product development timelines. Our manufacturing approach is structured to serve the changing needs of our clients, supporting small-quantity clinical or First-in-Human builds and can scale to accommodate full launch quantities. Vantage MedTech has facilities in Moonachie, New Jersey and Lenexa, Kansas. Visit www.vantagemedtech.com for more information

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