Roche Posted August 15, 2026

Global Lead PMO - Capex Project Excellence

Hillsboro, Oregon, United States of America FULL_TIME
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About this opportunity

The Position

At Roche, we are passionate about transforming healthcare. As a global leader in pharmaceuticals and diagnostics, we stay focused on our mission to improve the lives of patients through cutting-edge science and innovative technology. With a legacy spanning over 125 years, we pride ourselves on a culture that fosters integrity, courage, and passion. Joining Roche means becoming part of a diverse, multinational team dedicated to solving some of the world’s most complex medical challenges and delivering medical breakthroughs that make a real difference.

As the PMO Functional Lead for Execution Excellence within Pharma Technical Operations (PTT), you act as the strategic engine driving the predictable delivery of a global CAPEX portfolio. By blending high-performance standards with a lean, continuous-improvement mindset, you lead cross-functional teams in the industrialization and technical management of complex projects, ranging from lab upgrades to large-scale production facilities. Your role is pivotal in ensuring network-wide standardization, technical risk mitigation, and the optimization of manufacturing robustness, ultimately transforming execution into a reliable asset that supports the efficiency and reliability of the entire manufacturing network.

The Opportunity

Standardize Global Execution: You will develop and maintain the Global Project Management Playbook, ensuring all capital projects align with internal quality standards and industry-leading methodologies like PMBOK and PRINCE2.

Govern the Project Lifecycle: You will define and oversee the rigorous "Stage-Gate" process, ensuring critical peer reviews and readiness assessments are completed from conceptual design through to construction and validation.

Establish Execution Excellence: You will set the global standards for "Project Execution Plans" (PEP) to guarantee consistency, alignment, and operational excellence across all international Roche sites.

Drive Performance Transparency: You will implement a comprehensive suite of KPIs and Earned Value Management (EVM) metrics, providing high-level transparency into project health and execution efficiency.

Lead Strategic Governance: You will design and facilitate monthly Project Review Boards (PRB), offering executive-level insights into project risks, financial variances, and strategic mitigation plans.

Cultivate Risk Management: You will orchestrate a proactive risk-mitigation culture by leading "Cold Eyes" reviews and audits to identify execution gaps before they impact the critical path.

Institutionalize Knowledge: You will serve as the functional "Center of Excellence," leading Lessons Learned workshops and mentoring project staff globally to ensure continuous improvement and capability building.

Who you are

You possess an expert educational foundation, holding a Bachelor’s or Master’s degree in Engineering, Construction Management, or Business Administration, paired with a mandatory PMP or PgMP certification.

You are a seasoned leader in the field, bringing over 15 years of experience in capital project management, including at least 5 years leading a PMO within the Life Sciences or Process Industries.

You are an authority on project methodologies, offering deep expertise in Stage-Gate models, Lean Construction, and Agile project management to drive efficiency in complex environments.

You demonstrate advanced analytical proficiency, with the ability to utilize Primavera P6, MS Project, and BI tools like Tableau or Power BI to forecast costs and manage schedules effectively.

You are a strategic influencer, capable of navigating a complex matrix organization and building consensus among senior stakeholders to drive functional performance and organizational change.

You thrive as a mentor and coach, dedicated to developing organizational capability by guiding less experienced colleagues and identifying skill gaps within the project management community.

You are resilient and disciplined, showing an unwavering commitment to process adherence while maintaining the problem-solving skills necessary to recover off-track initiatives and navigate unprecedented challenges.

The expected salary range for this position based on the primary location of Oceanside is 127,900.00 - 237,500.00 USD Annual.   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/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 .

Job details

Seniority
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Hillsboro, Oregon, United States of America
Employment type
FULL_TIME

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 2526 comparable Manufacturing & CMC roles across 157 biopharma companies.

2526Comparable roles tracked
2230Currently active
157Companies hiring similar roles
61Countries represented

Salary context

639 of 2526 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · Sr Manufacturing Technician · Genz. Therap Product LP $2,400/yr – $3,200/yr
Highest disclosed · Executive Director, CMC Regulatory Science · ModernaTX, Inc. $224,900/yr – $404,600/yr
Peer group range $2,800 – $314,750 (median $122,900)

Where these roles are based

Top locations among the 2526 comparable roles

United States1157
India165
Germany152
Switzerland89
France89
Netherlands87

+ 55 more countries

Seniority mix

1056 of 2526 peers have a known seniority level

Senior320
Manager267
Associate129
Principal99
Associate Director90
Director86
Senior Director33
Intern/Fellow/Postdoc26
Executive/VP6

Therapeutic area mix

5 of 2526 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Rare Disease2
Vaccines & Infectious Disease1
Oncology1
Respiratory1

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How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

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Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.