Project Manager Combination Product (Contract)

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profile Job Location:

Providence, RI - USA

profile Monthly Salary: Not Disclosed
Posted on: 18 hours ago
Vacancies: 1 Vacancy

Department:

Project Management

Job Summary

Job Description

Role Overview

The Technical Project Manager supports medical device and drug-device combination product development programs (e.g. auto-injectors prefilled syringes on-body injectors). This role focuses on managing Design History File (DHF) documentation coordinating cross-functional technical activities and maintaining project timelines within a regulated environment.

Key Duties & Responsibilities

  • Lead multiple device/combination product projects with a discrete technical focus (e.g. auto-injectors injection pens on-body injectors prefilled syringes).
  • Manage and coordinate Design History File (DHF) documentation including compilation tracking and ensuring completeness of required documentation packages.
  • Develop and maintain detailed project timelines and work plans to support device development deliverables.
  • Partner cross-functionally with engineering quality regulatory and other technical teams to drive project execution and alignment.
  • Identify assess and proactively communicate project risks gaps and documentation deficiencies providing recommendations for resolution.
  • Track progress across multiple concurrent projects and adjust plans as needed to meet development milestones.
  • Facilitate project meetings document action items and ensure follow-through on commitments.
  • Support elements of technical project management including documentation workflows and coordination of device-related deliverables.
  • Contribute to process improvements and best practices within the combination product/device function.

Required Education

  • Typically requires a Bachelors degree in a project management or related discipline

Required Experience

  • Typically requires 5 years of relevant experience in medical device or drug-device combination product development.
  • Demonstrated experience supporting or managing device development programs (e.g. auto-injectors injection systems prefilled syringes on-body delivery systems).
  • Experience compiling or managing Design History File (DHF) documentation strongly preferred.
  • Experience working cross-functionally in regulated environments required.

Required Knowledge & Skills

  • Strong understanding of medical device development processes and documentation requirements.
  • Working knowledge of combination product development considerations.
  • Experience managing multiple concurrent technical projects in a regulated environment.
  • Ability to independently organize and manage documentation packages with high attention to detail.
  • Strong project planning and timeline management skills.
  • Direct confident communication style with the ability to work effectively across technical teams.
  • Ability to operate with limited oversight and quickly integrate into established development programs.

Contract Length: Through the end of the year.

Pay Range

$80/hr. - $90/hr.

Shift/Hours

Monday - Friday

Requisition Disclaimer

This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals (Vertex). The individual selected for this role will be offered the role as an employee of a third- party agency partner; compensation medical benefits fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors including skills competencies experience location and/or being pursued and other job-related factors permitted by addition this role will be eligible for overtime pay in accordance with federal and state requirements

By applying for this position you agree to the Atrium Terms and Conditions and you direct Atrium to share your application materials which may include your CV/Resume email address or phone number with Vertex. For more information on how Vertex handles your personal data related to your job application please see Vertexs Careers Privacy Notice. Agreeing to the Atrium Terms and Conditions includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings profiles articles news and other employment-related information as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners

(collectively Atrium Alerts). Atrium Alerts may be sent by email phone or text message. Your personal information will be safely stored within the Atrium & Vertex databases. Atrium does not sell your personal information to third parties. Text message and data rates may apply. To OPT OUT of text messaging or to modify your communication preferences for Atrium Alerts at any time please contact Atrium at .

If you do not agree with the Atrium Terms and Conditions you can still complete your application for this position by emailing your resume to our team at Please include the job title in the subject of your email.

No C2C or Third-Party Vendors


Required Experience:

IC

Job DescriptionRole OverviewThe Technical Project Manager supports medical device and drug-device combination product development programs (e.g. auto-injectors prefilled syringes on-body injectors). This role focuses on managing Design History File (DHF) documentation coordinating cross-functional t...
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Key Skills

  • Time Management
  • Data Analytics
  • Analytical
  • Agile
  • Requirement Gathering
  • Strategic thinking
  • Visio
  • Communication
  • Problem Solving
  • Market Research
  • UML
  • Cross Functional Teams