Sr. Project Manager, Global External Manufacturing

Posted 3 Days Ago
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San Rafael, CA, USA
In-Office
Senior level
Biotech • Pharmaceutical • Manufacturing
The Role
Leads end-to-end project delivery across global external manufacturing and site portfolios in a GMP-regulated environment. Builds integrated schedules, manages scope, risks, dependencies, resources, governance, and change control, and coordinates CMOs on technical transfers, validations, quality, engineering, and supply continuity initiatives. Provides data-driven decision support, executive updates, and continuous improvement while ensuring projects remain audit-ready and aligned with strategic and operational requirements. The hybrid role requires 10–20% travel to external partners.
Summary Generated by Built In

Who We Are
BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health.
Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities.
Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best – people with the right technical expertise and a relentless drive to solve real problems – and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we’ve produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options.
About Technical Operations
BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.

Sr. Project Manager, Global External Manufacturing

Hybrid - San Rafael, CA 2 Days On Site

Role Purpose

The Senior Project Manager drives disciplined, end-to-end project delivery across the GEO site portfolio and the global external manufacturing network, ensuring projects are planned, governed, and executed against approved scope, cost, and schedule in a highly regulated environment.

This role is accountable for independently building and maintaining integrated, logic driven project schedules, governing execution, and enabling timely, data driven decisions across new product introductions and continuous improvement initiatives. The Senior Project Manager serves as the critical link between portfolio planning and execution teams by translating complex technical and operational inputs into credible plans, clear tradeoffs, and actionable insights that support reliable delivery across GEO. 

Key Accountabilities

Project & Portfolio Management

  • Experience in project management of tech transfers, merger & aquisition-integrations required
  • Manage assigned projects through the full lifecycle, from intake and approval through execution, handover, and benefits realization.
  • Establish and maintain project charters, RAID logs, decision logs, and governance artifacts to ensure transparent, consistent, and audit‑ready oversight.
  • Ensure project scope, prioritization, and objectives remain aligned with strategic, operational, compliance, and capacity requirements across GEO.
  • Prepare and present concise, decision‑focused project reviews that synthesize progress, risks, issues, and required decisions for governance forums.
  • Lead and support continuous improvement initiatives by identifying recurring execution pain points, inefficiencies, and failure modes across projects, and partnering with stakeholders to improve processes, governance, and digital ways of working across GEO.

Project Planning & Schedule Ownership

  • Independently build, maintain, and optimize integrated project schedules using approved digital project management tools (e.g., MS Project or equivalent), including logic ties, milestones, dependencies, and critical paths.
  • Translate technical, quality, validation, and manufacturing inputs into credible, execution‑ready timelines, in partnership with SMEs.
  • Continuously analyze schedule health to identify drivers of slippage, downstream impacts, compression opportunities, and mitigation strategies.
  • Use schedule data to proactively surface risks, tradeoffs, and decision points for functional leaders and governance forums.

External Manufacturing (CMO) Project Delivery

  • Act as the structured project interface with CMOs to align deliverables, timelines, resource needs, and approval pathways.
  • Integrate CMO activities into end‑to‑end project schedules, ensuring external dependencies are logically linked and actively managed.
  • Support technical transfer, validation, quality, engineering, and supply continuity initiatives with internal and external teams.
  • Ensure documentation, change control, and execution activities meet GMP expectations and are inspection‑ready execution activities meet GMP expectations and are inspection ready.

Integration & Decision Support

  • Consolidate schedule, risk, and capacity data across projects to proactively surface decision needs and escalation items.
  • Explain not only what is happening, but why—clearly articulating root causes, leading indicators, and implications for scope, schedule, and resources.
  • Maintain decision logs ensuring actions, owners, and due dates are captured, tracked, and closed.

Resource, Risk & Dependency Management

  • Balance project resource demands with operational constraints, surfacing capacity conflicts, and dependency risks for timely escalation.
  • Maintain integrated views of critical paths, interdependencies, and mitigation actions across internal teams and CMOs.
  • Enforce disciplined risk management and change control to protect approved scope, schedule, and compliance commitments.

Stakeholder Engagement & Digital

  • Drive cross-functional alignment by setting clear expectations, resolving execution issues, and escalating risks that threaten delivery.
  • Prepare and deliver concise, decision-focused project updates to the Head of Strategy and Business Operations and senior stakeholders.
  • Support the evolution and consistent application of governance forums, standards, and ways of working to enable reliable execution, effective escalation, and cross-functional alignment across GEO.
  • Enable digital and data enabled ways of working by applying PMO standards, dashboards, and analytics to improve visibility, predictability, and governance effectiveness.

Qualifications

Education

  • Bachelor’s degree in Engineering/Science, Business, or Information Systems (or equivalent experience).
  • Project Management Profession (PMP) certification preferred
  • Lean Six Sigma Green Belt or higher preferred

Experience

  • Minimum 5 years’ experience in project management or business process improvement within a GMP-regulated manufacturing environment.
  • Proven experience independently building and managing complex project schedules with cross‑functional and external dependencies
  • Experience delivering or supporting technical transfers, validations, engineering changes, or portfolio projects.
  • Experience in external/contract manufacturing is an advantage.

Skills & Competencies

  • Exceptional communication skills with the ability to tailor messages for technical teams, operational leaders, and senior executives while maintaining clarity and alignment.
  • Demonstrates strong organizational awareness; understands decision-making dynamics and navigates matrixed environments effectively.
  • Influences and mobilizes cross-functional teams without direct authority through credibility, strong relationships, sound judgment, and consistent delivery.
  • Skilled in conflict management, facilitating difficult conversations and guiding teams toward constructive resolution.
  • Understanding of biopharma operations and compliance requirements.
  • Financial/business acumen with disciplined governance oversight.
  • Advanced digital literacy, demonstrated through hands‑on use of modern project management, analytics, and AI‑enabled tools to independently build and maintain integrated schedules, model dependencies and critical paths, analyze delivery risk, and translate data into decision‑ready insights (e.g., MS Project, Power BI, or equivalent).

Workstyle & Travel

  • Hybrid working model; travel to external partners as required (10–20%).

Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.
Equal Opportunity Employer/Veterans/Disabled
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Skills Required

  • Bachelor’s degree in Engineering, Science, Business, Information Systems, or equivalent experience
  • Minimum 5 years of project management or business process improvement experience within a GMP-regulated manufacturing environment
  • Experience independently building and managing complex project schedules with cross-functional and external dependencies
  • Experience delivering or supporting technical transfers, validations, engineering changes, or portfolio projects
  • Project management experience involving tech transfers and merger and acquisition integrations
  • Experience in external or contract manufacturing
  • Project Management Professional certification
  • Lean Six Sigma Green Belt certification or higher
  • Understanding of biopharmaceutical operations and compliance requirements
  • Advanced digital literacy, including integrated scheduling, dependency and critical-path analysis, delivery-risk analysis, and decision-support insights

BioMarin Pharmaceutical Inc. Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about BioMarin Pharmaceutical Inc. and has not been reviewed or approved by BioMarin Pharmaceutical Inc..

  • Healthcare Strength Benefits are often characterized as comprehensive, spanning medical, dental, vision, life and disability coverage, along with FSAs/HSAs and an EAP. Feedback suggests these health offerings are consistently regarded as strong and at times "industry best".
  • Leave & Time Off Breadth Leave and time off are described as generous, with structured vacation progression, dedicated sick time, and a company-observed winter break among many holidays. Feedback suggests this breadth of paid time away is a standout element of the total rewards.
  • Retirement Support Retirement support is underpinned by a 401(k) savings plan with a company match. Feedback suggests these retirement programs contribute meaningfully to overall compensation value.

BioMarin Pharmaceutical Inc. Insights

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The Company
HQ: San Rafael, CA
3,270 Employees
Year Founded: 1997

What We Do

Founded in 1997, BioMarin is a global biotechnology company dedicated to transforming lives through genetic discovery. The company develops and commercializes targeted therapies that address the root cause of the genetic conditions that it seeks to treat, helping to better the lives of those struggling with rare genetic disease. BioMarin discoveries have led to eight first or best-in-class commercial treatments and a pipeline of multiple product candidates applying the same science-driven, patient-forward approach to broader group of genetic disorders. The more innovative solutions developed, the more lives BioMarin can impact. Recruitment Fraud Alert Notice Please be aware of fraud or scams from individuals, organizations and/or internet sites claiming to represent BioMarin in recruitment activities. We have an established recruitment process which is required for all posted positions by BioMarin prior to issuing an offer of employment. This BioMarin process requires formal interviews conducted live with personnel representing BioMarin and never requires payments or fees from job applicants. BioMarin does not conduct interviews via texting tools such as RingCentral. In the event you receive a suspicious email message about recruiting on behalf of BioMarin, unless it’s from a BioMarin authorized recruiting partner, do not provide any personal information or pay any fees. Qualified and interested candidates should apply to current openings directly through this BioMarin website. BioMarin accepts no responsibility for any costs or charges incurred as a result of fraudulent activity. If you have lost money or provided your personal identifying information, please contact your bank and report the matter to the FBI via www.ic3.gov. We would also suggest you notify your local police department and monitor your credit. We appreciate your interest in BioMarin & encourage you to visit http://careers.biomarin.com/career-areas to review job opportunities.

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