Technical Program Manager

Reposted 10 Days Ago
Be an Early Applicant
Toronto, ON, CAN
In-Office
107K-139K Annually
Senior level
Healthtech • Other • Biotech
The Role
The Technical Program Manager will lead complex, cross-functional development programs in medical device technology, ensuring accountability, managing risks, and driving project execution from concept to launch.
Summary Generated by Built In

Why Orthofix?
    

Guided by our organizational values – Take Ownership | Innovate Boldly | Win Together – we collaborate closely with world-class surgeons and other partners to improve people’s quality of life. At Orthofix, we want team members who build relationships and share knowledge, challenge the status quo, and deliver results every day to help us achieve our vision to be the unrivaled partner in Med Tech.  

Our global team of over 1,600 employees brings to market highly innovative, cost-effective, and user-friendly medical technologies that heal musculoskeletal pathologies for patients and the healthcare professionals who treat them. Looking to change people’s lives? Look no further.

JOB PURPOSE

Do you take pride in owning complex programs end‑to‑end—and being the person who makes sure they actually get delivered?
If you are driven by execution, thrive in ambiguity, and enjoy being accountable for results from kickoff through commercial launch, this role is built for you.

As a Technical Program Manager in Orthofix’s newly created Product Portfolio Management & Execution team for Spine Enabling Technology (ET), you will be the execution owner for complex, high‑impact development programs. You will translate strategy and technical objectives into clear plans, integrated schedules, and daily execution, ensuring work moves forward across all functions.

You will actively drive programs across R&D, Manufacturing, Quality & Regulatory, and Marketing, managing dependencies, identifying risks early, and removing blockers as they arise. This role requires hands‑on leadership—tracking progress in detail, holding teams accountable to commitments, and continuously adjusting plans to keep programs on the critical path.

You will bring structure and rigor to complex development efforts by establishing clear milestones, decision points, and execution cadences, while ensuring stakeholders remain aligned and informed. Your ability to synthesize large amounts of information into concise, actionable status updates will support timely decision‑making at the development, leadership, and executive levels.

By driving disciplined execution, anticipating issues before they escalate, and maintaining relentless focus on delivery, you will directly impact time‑to‑market, program predictability, and successful commercialization of innovative Spine Enabling Technologies that support surgeons and improve patient outcomes.

ESSENTIAL FUNCTIONS AND RESPONSIBILITIES

The following are the essential functions of this position. This position may be responsible for performing additional duties and tasks as needed and assigned.

  • Lead complex, cross‑functional development programs from concept and feasibility through development, validation, transfer to manufacturing, and commercial launch.

  • Serve as the end‑to‑end execution owner, accountable for scope, schedule, budget, risk, and dependency management across multiple functional teams.

  • Drive day‑to‑day program execution by identifying issues early, escalating risks appropriately, and leading resolution of technical and operational blockers.

  • Partner closely with R&D (software, hardware, systems), Manufacturing, Quality & Regulatory, and Marketing, to ensure alignment to program objectives, priorities, and timelines.

  • Develop, maintain, and actively manage integrated program plans, complex schedules, milestones, and dashboards, ensuring focus on critical path and key deliverables.

  • Plan and facilitate program reviews, phase/gate reviews, and leadership readouts, delivering clear, concise, and actionable status updates to development, leadership, and executive stakeholders.

  • Monitor program performance using appropriate tools and techniques to track progress, identify variances, drive corrective actions, and communicate impacts and mitigation plans.

  • Ensure compliance with Orthofix development processes, company policies, and applicable medical device regulations and quality systems (e.g., ISO 13485, FDA design controls).

  • Support portfolio‑level planning and execution by providing visibility into program status, resource needs, risks, trade‑offs, and execution scenarios.

  • Lead effective program communication, meeting cadence, stakeholder alignment, and conflict resolution across internal and external teams.

  • Conduct project post‑mortems, capture lessons learned, and drive continuous improvement in program management practices.

  • Foster a collaborative, execution‑focused team environment by influencing without authority, building trust, and driving accountability.

MINIMUM QUALIFICATIONS

The requirements listed below are representative of the education, knowledge, skill and/or ability required for this position.

Education/Certifications:

  • Bachelor’s degree in Engineering (Mechanical, Biomedical, Electrical, Software, Systems) or equivalent technical discipline required.

Experience, Skills, Knowledge and/or Abilities:

  • 5-10 years of total professional experience, including:

    • 3+ years leading complex, cross functional programs or projects, and

    • 2+ years in regulated medical device development (capital equipment, instruments, systems, and/or software).

  • Strong execution mindset with demonstrated ability to drive multiple complex workstreams in parallel.

  • Proven capability to build, manage, and adapt complex, multi workstream schedules, balancing technical, regulatory, and operational dependencies.

  • Excellent critical thinking and problem solving skills, with a track record of proactively identifying issues and resolving blockers.

  • Exceptional written and verbal communication skills, including concise program level presentations and executive ready status reporting.

  • Highly organized with strong attention to detail; able to track schedules, risks, issues, dependencies, and commitments effectively.

  • Proven ability to build relationships, influence without authority, and align diverse stakeholders in a matrixed environment.

  • Working knowledge of medical device product development lifecycles, design controls, and phase/gate methodologies.

  • Sufficient technical depth to understand system level issues, support timely decision making, and manage change effectively.

  • Self-motivated, proactive, and comfortable operating in ambiguous environments.

  • Proficient in program management and scheduling tools (e.g., Smartsheet, Microsoft Project, Microsoft Office).

  • Willingness to travel up to 10-25% based on project requirements.

PREFERRED QUALIFICATIONS

The education, knowledge, skills and/or abilities listed below are preferred qualifications in addition to the minimum qualifications stated above.

Education/Certifications:

  • PMP or equivalent project/program management certification preferred but not required.

Additional Experience, Skills, Knowledge and/or Abilities:

  • Prior exposure to spine surgical systems, surgical navigation systems, and/or image‑guided surgery solutions.

  • Experience managing software‑enabled or system‑level medical devices (hardware + software + instruments).

  • Familiarity with global regulatory environments (FDA, EU MDR).

  • Knowledge of medical device industry best practices and trends. 

PHYSICAL REQUIREMENTS / ADVERSE WORKING CONDITIONS

The physical requirements listed in this section include, but are not limited, to the motor/physical abilities, skills, and/or demands required of the position in order to successfully undertake the essential duties and responsibilities of this position.  In accordance with the Americans with Disabilities Act (ADA), reasonable accommodations may be made to allow qualified individuals with a disability to perform the essential functions and responsibilities of the position.

  • No additional physical requirements or essential functions for this position.

The anticipated salary for this position for an employee who is located in Ontario is $107,183 to $138,587 per year, plus bonus, and benefits. The final pay offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and years of experience within the job, the type and years of experience within the industry, education, etc. The Company is a multi-jurisdiction employer and this pay scale may not reflect the pay scale for an employee who works in other countries or locations.

DISCLAIMER

The duties listed above are intended only as representation of the essential functions of this position.  The omission of specific statements of duties does not exclude them from the position if the work is similar, related, or a logical assignment to the position.  The job description does not constitute an employment agreement between the employer and employee and is subject to change at the sole discretion of the employer.  Nothing in this document alters an employee’s at-will employment status.

We are committed to providing equal employment opportunities to all employees and applicants without regard to race (including traits historically associated with race, such as hair texture and protective hairstyles, including braids, locks, and twists), ethnicity, religion, religious creed (including religious dress and grooming practices), color, caste, sex (including childbirth, breast feeding, and related medical conditions), gender, gender identity or expression, sexual orientation, national origin, ancestry, citizenship status, uniform service member and veteran status, marital status, pregnancy, age (40 and over), protected medical condition (including cancer and genetic conditions), genetic information, disability (mental and physical), reproductive health decision-making, medical leave or other types of protected leave (requesting or approved for leave under the Family and Medical Leave Act or the California Family Rights Act), domestic violence victim status, political affiliation, or any other protected status in accordance with all applicable federal, state, and local laws.

This policy extends to all aspects of our employment practices including, but not limited to, recruiting, hiring, discipline, termination, promotions, transfers, compensation, benefits, training, leaves of absence, and other terms and conditions of employment.

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The Company
HQ: Lewisville, TX
1,174 Employees
Year Founded: 1980

What We Do

Orthofix Medical Inc. began in a small farmhouse in Verona Italy in 1980 when orthopedic researcher Giovanni De Bastiani recognized the bone’s natural repair capability, a concept he called “dynamization.” With that in mind, he created the first external fixation device. Today, Orthofix has grown to more than 1,200 employees with locations in the U.S., Italy, Germany, France, the U.K., Brazil, and Australia. Our products help patients in more than 70 countries around the world. The Company’s mission is to deliver innovative, quality-driven solutions as we partner with health care professionals to improve patient mobility. Headquartered in Lewisville, Texas, the company has two strategic business units: Spine and Orthopedics. Orthofix products are widely distributed via the company's sales representatives and distributors. In addition, Orthofix is collaborating on research and development activities with leading clinical organizations such as MTF Biologics, the Orthopedic Research and Education Foundation, and the Texas Scottish Rite Hospital for Children.​ Orthofix makes a difference in the lives of others by providing our surgeon customers with innovative medical devices to meet the needs of their patients. Every day we are optimizing our operations, improving efficiencies, and examining our systems to provide the best support possible to our representatives, surgeons and patients.

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