Software Program Manager

**SOFTWARE PROGRAM MANAGER**

OncoRes Medical was founded at the intersection of medicine, science and humanity to improve
the accuracy of breast conserving surgery and eliminate the physical, psychological and economic
burdens associated with repeat operations.

Our unique, informal culture champions vision, restlessness and humanity. Knowing we have an
open and supportive team means each of us has the freedom to take responsibility and
ownership. We have a shared passion to work restlessly, pioneering change to re-imagine the
world, while remaining grounded in our commitment to science and quality.

Our passion for helping patients focusses us on the patient. We believe that all breast cancer
patients deserve the opportunity to move beyond their breast cancer surgery knowing that all the
cancer has been removed, the first time. In everything we do, we are thinking about how we can
inch closer to a world free from re-excisions... We are going BEYOND BREAST CANCER

**Overview**:
The Software Program Manager at OncoRes Medical is responsible for leading and managing the
overall software program with strong attention to strategy, implementation, and delegation, to
expected to lead a Software team and collaborate with Hardware, Clinical and Research Program
Managers and their corresponding team members. This is a key leadership role within OncoRes
Medical’s multidisciplinary Research and Development group.
If you want to use your expertise to help build a novel, disruptive medical product that will impact
the lives of millions of people around the world, get in touch This is a unique opportunity to get
involved in an early, rapidly growing company with significant growth and development

**Role**:

- In conjunction with the VP R &D, identifies a project portfolio pertinent to Software

Development.
- Elaborates project Work Breakdown Structures (WBS) to achieve Business Objectives.
- Monitors, Tracks and reports the WBS and Resource Utilisation.
- Monitors and tracks product related projects through formal Design Input, Design Output,

Verification, Validation and Design Transfer Phases.
- Ensures projects in the Software portfolio identify and synchronise project dependencies

between Program Managers.
- Ensures inputs from Research, Clinical and Market Development, can be captured by

Systems Engineering and if able to be adequately implemented, scheduled within project
timelines.
- Continuously identifies Design, Process or Product Risk and ensures that appropriate Risk

Mitigations have been identified in Design or Process Requirements.
- Ensures System Requirements, Design Requirements and Design Specifications have

Processes Validation records for Coverage and Traceability.
- Ensures all Design Specifications are Verified.
- Ensures the System Design has Design Validation records.

**Responsibilities**:

- Management of Software Development Resources.
- Delivery of a portfolio of Software Development Projects.
- Delivery of Software Project outcomes, on time and on budget.
- Collaborate and synchronise Project Portfolio tasks with Hardware, Research and Clinical

Program Managers.
- Operate within a Quality Management System (QMS) based on ISO 13485 and Risk

Management Processes based on ISO 14971.
- Delivery of Project, Development and Test documentation as Plans and Reports consistent

with QMS and ISO 62304 Software Lifecycle requirements.
- Delivery of Risk Analysis documentation consistent with QMS requirements.
- Delivery of Design Specification documentation consistent with QMS requirements.
- Ensures that the Design History File (DHF) for Software is maintained to QMS

requirements.
- Facilitate the autonomy of the Software Systems Engineer to elaborate System and Design

Requirements, respective Architectures and Risk Mitigations.
- Facilitate the Software Team autonomy to elaborate and implement Software Design

Specifications.
- Identification, elaboration, and triage of packages of Intellectual Property.
- Serve as an ambassador to promote OncoRes Medical’s core values; we are Inspired,

Restless, Human and Visionary.

**Qualifications**:

- Minimum Bachelor’s Degree in Computer Science or Engineering.
- Minimum 10 years’ product development experience.
- Minimum 5 years’ Project Management Experience.
- Minimum 3 years’ experience as a Lead in Software development.
- Demonstrable Safety Critical Systems development experience.
- Demonstrable Cross-Functional Team Management experience.
- Strong leadership Skills.
- Strong collaborative Skills.
- Strong documentation Skills
- Ability to remain professional and positive in all personal interactions, and work with

honesty and transparency while being committed to doing what’s best for our patients,
customers, and company.

**Desirable Experience**:

- Scrum Master Qualifications.
- Project Management Qualifications.
- Program Management Qualifications.
- Medical or Regulated Device development experience.

**Benefits**:

- Com