Position Description

The Project manager will be responsible for the coordination, implementation, control and integration of specific molecular oncology projects across multiple business units ensuring consistency with company strategy, commitments and goals.

 

Responsibilities

  • Provide clear assignments, common formats for their outputs, disciplined timelines, and coordinated meeting schedules, communication mechanisms and review processes
  • Facilitate integration planning of multiple projects across business units
  • Facilitate the definition of project scope, goals, and deliverables
  • Develop full scale project plans
  • Manage Design History File, Meeting Minutes, Risk Management Files, and project documentation
  • Schedule project timelines
  • Track project deliverables using appropriate tools
  • Provide support to project team and task forces
  • Present reports defining project progress, problems and solutions
  • Implement project changes and Interventions to achieve project outputs
  • Work with Product Management, Service, Systems Engineering and stakeholders to initiate, plan, development organizational structure to support projects
  • Will play a central role in planning and estimation of work required to meet product requirements
  • Will be able to create a work breakdown package and associated schedule using Microsoft Project Planner
  • Will create and maintain a project management plan and project risk together

 

Requirements

  • Bachelor’s degree is required in Bioengineering, Biomedical engineering, molecular, oncology or biology and/or a technical discipline is preferred or equivalent combination of education and experience
  • 2-3 years of direct work experience in a project capacity including M&A, business integration and plan development
  • Qualification in project management or equivalent
  • Knowledge of both theoretical and practical aspects of project management
  • Knowledge of project management techniques and tools
  • Direct work experience in project management capacity
  • Proven experience in FDA quality System Regulations (QSR) 21 CFR 820; Design Control: ISO
  • Proficient in MS Project, Office, and Outlook
  • Must be eligible to work in the U.S. as sponsorship is NOT available
  • Position is designated as on-site and is not available as remote

 

Key Competencies

  • Superior interpersonal and communication skills, both written and verbal
  • Team builder and team player
  • Strong analytical and problem solving skills
  • Adaptability

 

Preferred Qualifications

  • PMP (Project Management Professional) certification is highly preferred
  • Experience specifically with Molecular Diagnostic devices is desired

 

To apply, please forward your resume to Jenna Murray, Operations Manager and Human Resources Coordinator at jenna.murray@omniseq.com.