Engineer I, Project Management

Oregon, United States of America

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The Position


Project Portfolio Project Management

  • Executes the HTO Project Portfolio Management process and Portfolio Tools.
  • Monitors project performance information: report on the portfolio performance, contribution to the organization’s goals, and provide recommendations for action.
  • Drives adherence to defined processes and templates are sufficiently documented, maintained and followed (including monitoring of project realization phase)
  • Aligns portfolio planning with the annual planning/budgeting cadence
  • Educates departments on PPM process and tools
  • Determines if a project meets the criteria for the exception/emergency/non-standard process
    Tech Transfer Project Management
  • Perform necessary Project Control tasks.
  • Participate in the authoring of the Master Transfer Plan for tech transfers
  • Act as project manager, determining progress against the Master Transfer Plan
  • Participate in gap and risk analysis
  • Acts as a liaison with other sites to collect and review manufacturing data which demonstrate the nature and frequency of failure modes.
  • Collaborate with other departments to ensure studies are executed as designed and the results are well documented
  • Sign documents for activities as authorized and described by Genentech policies and procedures and job descriptions
  • Support the change management system
  • Participate in the design and implementation of department and cross-functional initiatives
  • Apply advanced theory, technical principles, and expert judgment to address a broad range of difficult problems
  • Identify, design, and implement process and system improvements
  • Manage competing priorities
  • Perform any other tasks as requested by Management to support MSAT activities

Qualifications / Requirements:

  • B.A. or B.S. degree (preferably engineering) and a minimum of 3-5 years of project management and/or tech transfer experience in the pharmaceutical or biopharmaceutical industry (preferably drug product manufacturing)
  • Knowledge of cGMPs or equivalent regulations
  • Ability to make sound decisions about scheduling, allocation or resources, and managing priorities
  • Ability to interpret and relate Quality standards for implementation and review
  • Ability to communicate clearly and professionally both in writing and verbally
  • Flexibility in problem solving, providing direction and work hours to meet business objectives
  • Project Portfolio Management experience is preferred but not required
  • Ability to interpret Genentech standards and practices for implementation and review

Who We Are

A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry for more than 40 years, using human genetic information to develop novel medicines for serious and life-threatening diseases. Genentech has multiple therapies on the market for cancer & other serious illnesses. Please take this opportunity to learn about Genentech where we believe that our employees are our most important asset & are dedicated to remaining a great place to work.

The next step is yours. To apply today, click on the "Apply online" button.

Genentech is an equal opportunity employer & prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital & veteran status. For more information about equal employment opportunity, visit our Genentech Careers page.

At Genentech, we share salary ranges with applicants during the recruiting process, if requested. Third party salary estimates may not be accurate or up-to-date.

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