An exciting opportunity within the medical devices industry for a Program Director based in Cape Town. Our client seeks a highly competent, efficient, thorough, and hardworking Program Director. The ideal candidate should have a strong technical background, demonstrate leadership, project management, and business & technical initiative, and possess excellent interpersonal and time management skills. Successful candidates will be exposed to a wide range of projects within the Medtech space, offering significant professional growth opportunities.
Responsibilities:
- Interface with customers to understand their needs and assess fit with current & future capabilities.
- Prepare project plans & resource allocations to present to customers with support from the team (MD, Senior Engineering, etc.).
- Manage external projects: kick-off customer projects, handle routine feedback (meetings & written), manage timeline change communication, and ad hoc communication.
- Manage internal resources: identify and assign resources to projects, monitor resources across projects, leverage technical expertise, and coach/mentor R&D staff.
- Conduct high-level program analysis & reporting.
- Implement actionable items such as system identification, building & optimization, staff/contractor recruitment or release, materials & equipment management.
- Strategic planning and goal setting: establish program goals, develop policies, and design initiatives aligned with organizational objectives.
- Resource management: allocate resources effectively, including budgeting and staffing, ensuring programs stay within budget.
- Oversee program implementation and delivery, ensuring objectives are met.
- Coordinate efforts across departments or teams to ensure program success.
- Monitor and evaluate program performance, making adjustments as needed.
- Lead and supervise program staff, providing guidance, training, and support.
- Engage with external stakeholders such as community members, clients, or partners to ensure alignment and success.
Requirements:
- MSc., MASc., or BEng. in Mechanical, Electrical, Mechatronics, or Biomedical Engineering.
- 10+ years of experience in medical device development.
- Proficiency in SolidWorks CAD.
- Experience with Class III medical device R&D, preferably in cardiovascular devices.
- Experience interfacing with suppliers for timely delivery of products and services.
- Hands-on technical expertise in quality control, testing, jig design, implant & catheter design, 3D printing, polymer fabrication, and testing.
- Experience with project documentation, regulatory pathways, and intellectual property management.
- Strong organizational and administrative skills, including handling POs, NDAs, timesheets, and test protocols.
Desired Skills:
- Program Director
- Project Management
- Biomedical Engineering
- SolidWorks CAD
- Medical Devices, especially Cardiovascular Devices
- Class III Device Experience