Employer Industry: Medical Device Manufacturing

Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Supportive and collaborative work environment
- Chance to work on innovative projects in a regulated medical device environment
- Engage with diverse stakeholders and teams
- Utilize project management tools and methodologies to enhance job performance

What to Expect (Job Responsibilities):
- Develop project charters and management plans, recommending trade-offs as needed
- Define and manage project scope and major workstreams with management approval
- Create detailed Gantt charts and manage sub-project timelines for timely task completion
- Identify and manage project risks, including creating risk registers and response plans
- Prepare stakeholder registers and communication plans for assigned projects

What is Required (Qualifications):
- Bachelor's degree (or equivalent) in Business, Engineering, or Project Management
- Minimum of 5 years of relevant project management experience, preferably in a regulated or medical device environment
- Strong self-motivation and accountability to achieve goals
- Ability to effectively communicate and present ideas to diverse audiences
- Proficiency in project management tools like PPM systems, MS Office, SharePoint, or Visio

How to Stand Out (Preferred Qualifications):
- Certifications such as PMP, CAPM, or equivalent
- Familiarity with EU MDR and FDA medical device requirements
- Previous experience in a regulated environment
- Proficiency in project management software like MS Project, Planview, JIRA, or Trello

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