Gilead Sciences, Inc. Posted October 7, 2026

Global Manufacturing ERP Strategy Lead

Foster City, United States Full time
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Gilead Sciences, Inc. is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.

Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.

Job Description

This role serves as the Manufacturing Global Process Owner (accountable for 1 or more Level 1 process steps) for the in-scope ERP-enabled processes and data for production planning, ensuring that global standards, controls, decision rights, and performance measures support compliant, agile, and cost-effective supply.

Reporting to the Head of Global Manufacturing Strategy and Operations, this leader connects Manufacturing operations, Supply Chain, Quality, Finance, and IT to translate shop-floor and business needs into standardized, scalable processes enabled by SAP S/4HANA and related Manufacturing systems. The role contributes to Manufacturing process strategy and leads the development and execution of standards, governance, data, performance measures, business outcomes, and long-term process stewardship across Clinical and Commercial Manufacturing,. The role also supports migration to the AI enabled and cloud-based RISE platform, enabling a unified digital backbone for manufacturing operations. This is a unique opportunity to shape the future of digital manufacturing in a dynamic, science-driven environment.

Job Responsibilities 

Establish and own the target-state process architecture, governance, and Manufacturing business roadmap for ERP-enabled processes. Define and standardize global Manufacturing processes across internal Clinical and Commercial Manufacturing sites and applicable CMOs, and translate approved priorities into business requirements for incorporation into the integrated ERP transformation roadmap.

Define the performance metrics and decision frameworks to ensure long-term sustainability, compliance, and continuous improvement of our business processes associated with Manufacturing digital systems.

Lead ERP-enabled end-to-end process mapping and optimization to deliver medicines from development to commercial and from production planning to customer shipment.

Lead cross-functional Manufacturing process governance with representatives from IT, Finance, Manufacturing, Supply Chain, Quality, and Regulatory. Approve Manufacturing process standards, business requirements, controls, and data definitions; provide timely business decisions and escalation; and partner with the ERP Transformation Lead to ensure that solution design, deployment sequencing, and adoption remain aligned with approved Manufacturing outcomes and enterprise standards.

Own Manufacturing business readiness and adoption for approved process changes, including stakeholder alignment, role and procedure impacts, training requirements, adoption measures, and sustainment. Partner with change-management resources on the integrated change plan, deployment communications, and release readiness.

Forecast and manage Capital Expenditure (CAPEX), Operational Expenditure (OPEX), and headcount/resource budgets for deployment and sustainment of Global Manufacturing systems and assets.

Lead and develop the matrixed Global Manufacturing ERP process-owner network, including Manufacturing business analysts, site process leads, subject-matter experts, and super users. Establish role expectations, decision forums, capability development, and sustainment mechanisms while coordinating deployment assignments and capacity needs with the ERP Transformation Lead.

Serve as the Global Process Owner and Manufacturing data owner for the in-scope ERP-enabled processes. Approve process standards, controls, data definitions, and business decisions; ensure inspection readiness of Manufacturing process governance and evidence; and partner with system owners, Quality, IT, and the ERP Transformation Lead for audit and Health Authority interactions involving the SAP platform.

Set Manufacturing business priorities and outcome requirements for SAP S/4HANA, RISE, AI-enabled capabilities, and related global systems. Evaluate opportunities against process, compliance, data, and value objectives, and partner with the Manufacturing Digital leader, PDM SAP Tower, IT, and the ERP Transformation Lead to align the Manufacturing process roadmap with the enterprise solution and technology roadmaps.

Demonstrate Gilead Leadership Commitments through visible, values‑driven leadership, inclusive decision‑making, and clear accountability.

Model inclusive, transparent decision-making, combining diversity in thought and perspective with consistency and clarity in accountability.

Qualifications 

Requires a Bachelors degree with 12+ years of relevant professional experience or Masters degree or Ph.D. with 10+ years of relevant professional experience – a degree in a relevant scientific or business discipline is strongly preferred.

Proven experience leading large-scale SAP implementations in a manufacturing or life sciences environment, including the ability to translate GMP manufacturing needs into technical user requirements specifications for Information Technology teams.

Extensive ERP experience as a user and business process owner, including familiarity with typical transactions and master data configuration.

Deep understanding of cGMP clinical and commercial manufacturing operations, planning, supply chain, and regulatory requirements.

Excellent business acumen, organizational and communication (both written and verbal) skills.

Proven ability to lead complex, global transformation initiatives, influence stakeholders without authority, manage ambiguity, and drive adoption through effective communication and change leadership.

Excels at coaching others and utilizing analytical problem-solving skills to anticipate both strategic and operational issues and recommend effective solutions.

Strategic thinking and ability to constructively challenge the status quo.

Demonstrated experience leading global process standardization initiatives and serving as a business and data owner across complex, interconnected digital ecosystems.

Strong influencing skills with experience as a direct or matrixed people leader with responsibility for areas of significant business impact in a global environment.

Ability to manage multiple priorities, to draw out diverse views, and to effectively manage challenging conversations with tact and empathy.

Demonstrated ability to lead organizational change initiatives that adapt to differences in organizational cultures and norms, including stakeholder engagement, communication planning, and adoption strategies.

Preferred Qualifications

Black Belt or higher certification in Lean / OE / Six Sigma

Supply Chain APICS / ASCM certification

Experience designing and building a global capabilities center or similar shared‑services workforce to provide enterprise‑level system support

The salary range for this position is: $210,375.00 - $272,250.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.

For additional benefits information, visit:

https://www.gilead.com/careers/compensation-benefits-and-wellbeing

* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.

For jobs in the United States:

Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex , age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact ApplicantAccommodations@gilead.com  for assistance.

For more information about equal employment opportunity protections, please view the  'Know Your Rights' poster.

NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT

YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT

Gilead Sciences will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the  legal duty to furnish information; or (d) otherwise protected by law.

Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.

Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.

For Current Gilead Employees and Contractors:

Please apply via the Internal Career Opportunities portal in Workday.

Job details

Seniority
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Foster City, United States
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 3753 comparable Manufacturing & CMC roles across 173 biopharma companies.

3753Comparable roles tracked
3372Currently active
173Companies hiring similar roles
64Countries represented

Salary context

920 of 3753 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 $210,375/yr – $272,250/yr
Lowest disclosed · Biologics Support Operator I (3rd Shift) · AbbVie $14/hr – $26/hr (≈ $29,099–$54,122/yr)
Highest disclosed · Head of Analytical Development · ModernaTX, Inc. $272,200/yr – $490,100/yr
Peer group range $41,610 – $381,150 (median $125,375)

Where these roles are based

Top locations among the 3753 comparable roles

United States1738
Germany251
India166
France146
Ireland137
China123

+ 58 more countries

Seniority mix

1670 of 3753 peers have a known seniority level

Senior431
Manager381
Intern/Fellow/Postdoc259
Associate162
Principal138
Associate Director119
Director115
Senior Director57
Executive/VP8

Therapeutic area mix

24 of 3753 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease15
Rare Disease3
Oncology3
Respiratory1
Dermatology & Aesthetics1
Immunology1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
AstraZeneca New Haven, Connecticut, United States of America
Same function Same country
40%similar
40%similar
Lilly Indianapolis, Indiana, United States of America Director
Same function Same country
40%similar
Lilly Indianapolis, Indiana, United States of America Director
Same function Same country
40%similar
Lilly Indianapolis, Indiana, United States of America Intern/Fellow/Postdoc
Same function Same country
40%similar
Lilly Indianapolis, Indiana, United States of America Intern/Fellow/Postdoc
Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Manufacturing & CMC job in the United States, and choose locations and companies.

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.

40%
Development Scientist III, Analytical Development and Clinical Quality Control
AstraZeneca · New Haven, Connecticut, United States of America · Seniority not listed
Function Therapeutic area Seniority Country
40%
Director - Analytical Chemistry
Lilly · Indianapolis, Indiana, United States of America · Director
Function Therapeutic area Seniority Country
40%
Director - BRD Analytical Development
Lilly · Indianapolis, Indiana, United States of America · Director
Function Therapeutic area Seniority Country
40%
Analytical R&D Fellowship – Formulation and Solubility Studies (Hiring Our Heroes Corporate Fellow)
Merck · West Point, Pennsylvania, United States · Intern/Fellow/Postdoc
Function Therapeutic area Seniority Country
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.