Project Coordinator

jobr.pro

Sunnyvale (CA)

On-site

USD 70,000 - 90,000

Full time

14 days+

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Job summary

jobr.pro in Sunnyvale, California is looking for a Project Coordinator to support complex product development programs within Advanced Engineering. The role involves ensuring timely execution of deliverables across various subsystems and facilitating governance.

The ideal candidate has a Bachelor’s degree and at least 3 years of project coordination experience, with strong communication skills and familiarity with Agile methodologies. The position offers growth opportunities in a dynamic environment.

Qualifications

  • 3+ years of experience in project coordination or program management.
  • Good organizational skills and proactive problem solving.
  • Ability to manage multiple projects simultaneously.

Responsibilities

  • Support complex, cross-functional product development programs.
  • Track project plans, risk management, and deliverables.
  • Coordinate meetings, taking minutes and following up on action items.

Skills

Project coordination
Risk management
Regulatory submissions
Verbal and written communication
Agile methodologies

Education

Bachelor’s Degree

Tools

Word
Excel
PowerPoint
JIRA
Oracle/Agile

Job description

Job Description

Primary Function of Position:

The Project Coordinator will support complex, cross‑functional product development programs within Advanced Engineering. This role ensures timely execution of deliverables across subsystems including Instruments, Vision, Software, and Clinical, with a focus on regulatory and clinical readiness. The coordinator will drive operational efficiency, facilitate governance, and support logistical and tactical workstreams as well as strategic initiatives such as V&V deliverables and regulatory submissions.

Job Requirements
  • Work with Program Managers tracking project plans, risk management plans, documentation, and tasks
  • Succinctly monitor and report status: project milestones, documentation, action items, and deliverables
  • Coordinate activities defined by the Program or Project Managers
  • Support meetings including taking minutes and tracking action items
  • Closely track Verification and Validation protocols and reports for Regulatory submissions
  • Coordinate logistics related to clinical study readiness and execution including supporting device shipments to clinical sites, tracking and receiving
  • Strong collaboration and direct participation with Regulatory during final preparations for submissions
  • Agile (ACCS) originator experience initiating ECOs
  • Setup Design History File (DHF) structure; work with team to ensure DHFs are updated and accurate
  • Coordinate design and phase gate reviews including assembling presentations, checklists, and action items
  • Liaison with Document Control and ECO Change Control Board (CCB) to ensure timely approval
  • Familiar with software terminology and software development lifecycle activities and deliverables
  • Familiarity tracing documentation in accordance to medical device design control requirements is highly desirable
Qualifications

Skills, Experience, Education, & Training:

  • Bachelor’s Degree
  • 3+ years of experience in project coordination or program management
  • Good organizational and investigative skills; proactive problem solving
  • Excellent verbal and written communication skills
  • Ability to quickly switch between many different projects
  • Familiar with waterfall and SCRUM project management
  • Proficient in Word, Excel, PowerPoint, Project, Smartsheet, or other similar tools
  • Proficient in ALM tools (such as MKS or Polarion), Oracle/Agile, and JIRA
  • Specialized training in a discipline such as computers and/or planning and scheduling

Preferred Skills and Experience:

  • Masters degree
  • 2+ years of project coordination or program management experience within a technical or regulated or medical devices environment

Due to the nature of our business and the role, please note that Intuitive and/or your customer(s) may require that you show current proof of vaccination against certain diseases including COVID-19. Details can vary by role.

We are an AA/EEO/Veterans/Disabled employer.

Intuitive is an Equal Opportunity Employer. We provide equal employment opportunities to all qualified applicants and employees, and prohibit discrimination and harassment of any type, without regard to race, sex, pregnancy, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status, genetic information or any other status protected under federal, state, or local applicable laws.

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