Salary
💰 $149,700 - $224,600 per year
About the role
- Our Diagnostics portfolio is comprised of in-vitro diagnostic products and services that we offer to healthcare providers in the fields of laboratory diagnostics and point-of-care diagnostics.
- Serving a broad selection of diagnostic test settings – from centralized reference and hospital laboratories to critical care, emergency departments, and physician office laboratories – our comprehensive portfolio covers a range of testing disciplines, including immunochemistry, hematology, coagulation, urinalysis, blood gas analysis, and molecular tests.
- Our diagnostics business is in the midst of a transformation, and we are looking for a remote Strategic Project/Program Director in our PMO to help us define and execute on our vision.
- If you are passionate about making a difference in the field of diagnostics and believe you would be a great fit for this position, apply now for the role of Strategic Project/Program Director.
- This is a role well suited to an ambitious professional, looking for the next step in their career.
- The description includes Your role You have comprehensive training in Project Management disciplines and ample experience in managing assay Product Development projects.
- Your role You have strong leadership capabilities to lead diverse teams of non-direct reports from multiple functional areas in a matrix organization.
- You have the ability to coordinate across disciplines and integrate all business aspects as they impact product development and non-product development projects, including negotiation of scope, roles and responsibilities, specifications, timelines, and resources - across the organization.
- You have experience working with cross-functional teams across multiple geographies to develop, implement and manage detailed project plans including timelines, resources and budgets.
- You have the ability to analyze project constraints and risks to identify mitigations and opportunities.
- You possess strong analytical skills to assess situations, identify root causes and drive decision making.
- You are an effective written and oral communicator. Tailoring your approach to meet the needs of all stakeholders at all levels.
- You have the ability to relate well and establish credibility with senior leadership.
- You have attention to quality in all activities and initiatives.
- You have the required knowledge to ensure that project activities comply with FDA and other regional regulatory requirements.
- Your expertise Technical bachelor’s degree such as in Engineering or Life Sciences required
- 10+ years of industry experience, which includes minimum 4 years’ experience managing complex enterprise projects
- Knowledge and experience working in a highly regulated industry
- Ability to influence stakeholders without direct authority.
- Strong communication and presentation skills.
- PMP certification not required but strongly preferred and is a key differentiator
Requirements
- comprehensive training in Project Management disciplines and ample experience in managing assay Product Development projects
- strong leadership capabilities to lead diverse teams of non-direct reports from multiple functional areas in a matrix organization.
- the ability to lead diagnostic assay development projects to deliver against the project business case to maintain the project Value Proposition
- coordinate across disciplines and integrate all business aspects as they impact product development and non-product development projects, including negotiation of scope, roles and responsibilities, specifications, timelines, and resources - across the organization.
- experience working with cross-functional teams across multiple geographies to develop, implement and manage detailed project plans including timelines, resources and budgets
- the ability to analyze project constraints and risks to identify mitigations and opportunities
- strong analytical skills to assess situations, identify root causes and drive decision making.
- effective written and oral communicator. Tailoring your approach to meet the needs of all stakeholders at all levels.
- the ability to relate well and establish credibility with senior leadership.
- attention to quality in all activities and initiatives.
- the required knowledge to ensure that project activities comply with FDA and other regional regulatory requirements.
- Technical bachelor’s degree such as in Engineering or Life Sciences required
- 10+ years of industry experience, which includes minimum 4 years’ experience managing complex enterprise projects
- Knowledge and experience working in a highly regulated industry
- Ability to influence stakeholders without direct authority.
- Strong communication and presentation skills.
- PMP certification not required but strongly preferred and is a key differentiator