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Project Manager Biotech Jobs in Oregon (NOW HIRING)

Genentech, Inc.

Principal Project Scheduler

Hillsboro, OR · On-site

$119K - $222K/yr

As Lead Scheduler, you will be the scheduling expert and strategic partner for complex biotech ... You will serve as the primary scheduling expert, facilitating collaboration, managing competing ...

Genentech

Principal Project Scheduler

Hillsboro, OR

$119K - $222K/yr

As Lead Scheduler, you will be the scheduling expert and strategic partner for complex biotech ... You will serve as the primary scheduling expert, facilitating collaboration, managing competing ...

Parexel

OR · On-site

... size biotech/ pharma clients. Individuals selected for these roles will provide leadership to project teams and manage the day-to-day operations while striving to achieve operational excellence ...

Natera

Manager, Software Engineering

OR · On-site +1

... fast-growing biotech company. The team will support bleeding edge research focused on the ... Manage * Manage multiple ongoing projects * Identify project objectives, the scope of software ...

Iff

Manufacturing Technology Manager

Clackamas, OR · On-site

Lead the Manufacturing Technology function at a large-scale industrial biotechnology site, managing both project portfolios and team performance. * Develop and mentor a multidisciplinary engineering ...

Natera

OR · On-site

... in biotech space and educational background in molecular biology or genetics testing * Certification or formal training in Program or Project Management and experience using a resource management ...

Telix Pharmaceuticals (AMER)

OR · On-site

$114K - $142K/yr

... biotechnology industry experience including direct experience in oncology drug development required * 5+ years' project and budget management experience * Non-clinical through Phase 4 experience an ...

Burke Porter Group

Program Manager

Corvallis, OR · On-site

Experience * 10+ years of program or project management experience in a CDMO, medical device, biotech, or regulated manufacturing environment. * Demonstrated experience owning program financials ...

Amgen

OR · On-site

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Ensure projects move efficiently through internal review processes and are executed with excellence ...

Amgen

OR · On-site

$88K - $118K/yr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Project managing planned and ad-hoc special projects within Contract Development and U.S. Value ...

Iff

Manufacturing Technology Manager

Clackamas, OR

Lead the Manufacturing Technology function at a large-scale industrial biotechnology site, managing both project portfolios and team performance. * Develop and mentor a multidisciplinary engineering ...

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All JobsProject Manager Biotech JobsProject Manager Biotech Jobs in Oregon

Project Manager Biotech information

See Oregon salary details

$23

$48

$80

How much do project manager biotech jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for project manager biotech in Oregon is $48.89, according to ZipRecruiter salary data. Most workers in this role earn between $42.45 and $53.61 per hour, depending on experience, location, and employer.

What is the difference between Project Manager Biotech vs Clinical Project Manager?

AspectProject Manager BiotechClinical Project Manager
CredentialsBachelor's or Master's in Life Sciences, Project Management CertificationBachelor's or Master's in Life Sciences, Clinical Research Certification
Work EnvironmentBiotech companies, R&D labs, manufacturingClinical trial sites, hospitals, pharmaceutical companies
Industry UsageBiotech product development, research projectsClinical trial management, regulatory compliance
Common Search/ComparisonYesYes

The main difference between a Project Manager Biotech and a Clinical Project Manager lies in their focus areas. The Project Manager Biotech oversees research and development projects within biotech companies, focusing on product development and manufacturing. In contrast, the Clinical Project Manager specializes in managing clinical trials, ensuring regulatory compliance and patient safety. Both roles require strong project management skills and relevant certifications, but they operate in different phases of the biotech and pharmaceutical industry.

How does a Project Manager in biotech typically collaborate with cross-functional teams to drive project success?

A Project Manager in the biotech sector routinely works with cross-functional teams that include scientists, regulatory experts, manufacturing staff, and quality assurance professionals. They coordinate meetings, align project timelines, and ensure clear communication of goals and milestones. Effective collaboration involves resolving conflicts, facilitating information flow among departments, and adapting plans as scientific or regulatory requirements evolve. This collaborative approach is essential for keeping projects on track, maintaining compliance, and achieving successful outcomes in a highly regulated and fast-paced industry.

What does a Project Manager in Biotech do?

A Project Manager in Biotech is responsible for planning, coordinating, and overseeing projects within biotechnology companies or research organizations. They work closely with scientists, regulatory teams, and other stakeholders to ensure that projects meet deadlines, stay within budget, and comply with industry regulations. Their tasks may include setting project timelines, managing resources, mitigating risks, and communicating progress to leadership. Project Managers play a crucial role in bringing new biotech products or research initiatives from conception to completion.

What are the key skills and qualifications needed to thrive as a Project Manager in Biotech, and why are they important?

To thrive as a Project Manager in Biotech, you need a solid background in life sciences or engineering, experience in project management, and often a relevant degree such as a BSc or MSc, sometimes complemented by a PMP certification. Familiarity with project management software (such as MS Project or Jira), regulatory compliance systems, and budgeting tools is frequently required. Strong leadership, problem-solving, and effective communication skills set standout candidates apart by enabling them to coordinate cross-functional teams and manage complex timelines. These skills are essential to ensure that projects meet regulatory standards, stay on schedule, and achieve scientific and business goals.
What are popular job titles related to Project Manager Biotech jobs in Oregon? For Project Manager Biotech jobs in Oregon, the most frequently searched job titles are:
What job categories do people searching Project Manager Biotech jobs in Oregon look for? The top searched job categories for Project Manager Biotech jobs in Oregon are:
What cities in Oregon are hiring for Project Manager Biotech jobs? Cities in Oregon with the most Project Manager Biotech job openings:
Project Manager Biotech jobs near you
Principal Project Scheduler

Principal Project Scheduler

Genentech, Inc.

Hillsboro, OR • On-site

$119K - $222K/yr

Full-time

Posted 25 days ago

Genentech rating

9.0

Company rating: 9.0 out of 10

Based on 21 frontline employees who took The Breakroom Quiz

7th of 71 rated pharmaceutical

Job description

This role is a valuable part of Roche's Global Engineering team within Pharma Technical Operations, which is committed to delivering world-class capital projects that enable our GMP manufacturing excellence and innovation. As Lead Scheduler, you will be the scheduling expert and strategic partner for complex biotech projects, collaborating closely with cross-functional teams, contractors, vendors, and leadership across multiple sites in a defined region to ensure projects are delivered on time and within scope. You will have the opportunity to apply advanced planning methodologies, including Lean Construction and Last Planner® System practices, while influencing project outcomes and supporting our commitment to operational excellence. This position offers the chance to work on diverse, high-impact initiatives while building a reputation as a trusted advisor in complex project scheduling.
The Opportunity
As the Principal Project Scheduler you will develop and maintain integrated project master schedules for complex GMP biotech capital projects, ensuring alignment across multi-disciplinary teams and stakeholders while applying Roche standards and best practices. You will serve as the primary scheduling expert, facilitating collaboration, managing competing demands, and providing strategic schedule analysis and recommendations to keep projects on track.
  • You will develop comprehensive Integrated Project Master Schedules in accordance with Roche standards and the Engineering Manual, including baseline establishment and contingency planning for complex, multi-phase GMP biotech projects
  • You will collaborate with project teams to establish Work Breakdown Structures, work packages, and discipline schedules; conduct technical integrity reviews of contractor and vendor schedules for logic soundness and accuracy
  • You will facilitate pull planning sessions and lead the implementation of Last Planner® System and Lean Construction methodologies to optimize project execution and stakeholder alignment
  • You will perform advanced schedule analysis including critical path analysis, float trend analysis, earned value assessments, and Monte Carlo risk simulations; provide forecasting and recommendations for corrective actions
  • You will support RFP preparation, bid reviews, and vendor/contractor evaluations to assess schedule performance capabilities and ensure project alignment
  • You will monitor project progress through regular site walks and schedule updates; provide timely status reporting, variance analysis, and early warning identification to keep stakeholders informed and engaged
  • You will assist with strategic planning, "what-if" scenario analyses, change management, and resource/cost-loaded scheduling to support informed decision-making across the project lifecycle

Who You Are
  • Expert Schedule Professional: You hold a Bachelor's degree in Engineering, Economics, or Business Administration with a minimum of 8 years (6 with Masters) of experience as a project schedule engineer, backed by PMI or ACCEi Project Control Professional certification or equivalent qualification
  • Biotech & GMP Specialist: You bring hands-on experience with biotech or pharmaceutical CAPEX projects, with deep knowledge of how Commissioning, Qualification, Validation, and Automation integrate within complex GMP manufacturing environments
  • Skilled Matrix Collaborator: You excel at facilitating understanding and alignment across multi-disciplinary groups, managing competing stakeholder demands, and influencing outcomes in matrixed environments through exceptional communication and interpersonal skills
  • Advanced Technical Capability: You demonstrate proficiency in Primavera P6, MS Project, Monte Carlo simulation software (Pertmaster, Safran Risk), and MS Office; you possess strong knowledge of Earned Value Management, Last Planner® System, and Lean Construction methodologies
  • Strategic Problem Solver: You bring excellent analytical skills with the ability to interpret complex data, provide actionable insights, and support project teams in navigating challenges and optimizing schedules across diverse, high-complexity initiatives

The expected salary range for this position based on the primary location of Hillsboro is $119,000 - $222,000. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed in this link.
This is an on-site position; no remote options are available at this time.
Relocation benefits are not approved for this posting.
Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

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About Genentech

Sourced by ZipRecruiter

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.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

South San Francisco, CA, US

Year founded

1976

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