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Biotechnology Project Manager Jobs in Santa Rosa, CA

Bachelor's degree in a science-related field or engineering OR associate's degree/biotech ... management, and outplacement services on a global basis. Kelly has evolved from a United States ...

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Biotechnology Project Manager information

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How much do biotechnology project manager jobs pay per hour?

As of Aug 4, 2026, the average hourly pay for biotechnology project manager in Santa Rosa, CA is $50.56, according to ZipRecruiter salary data. Most workers in this role earn between $43.89 and $55.43 per hour, depending on experience, location, and employer.

What does a biotechnology project manager do?

A Biotechnology Project Manager oversees and coordinates projects within the biotechnology industry, ensuring that research and development initiatives, product launches, or clinical trials are completed on time and within budget. They work with cross-functional teams, including scientists, engineers, and regulatory experts, to set project goals, manage resources, and monitor progress. Their responsibilities also include risk management, stakeholder communication, and ensuring compliance with industry regulations. This role is vital for driving innovation and bringing new biotech products or solutions to market efficiently.

What is the difference between Biotechnology Project Manager vs Research Scientist?

AspectBiotechnology Project ManagerResearch Scientist
Required CredentialsBachelor's or Master's in Biotechnology, Project Management certification often preferredMaster's or PhD in Biotechnology or related field
Work EnvironmentProject teams, corporate labs, industry settingsResearch labs, academic institutions, industry research divisions
Employer & Industry UsageBiotech companies, pharmaceutical firms, biotech startupsUniversities, research institutes, biotech companies

The main difference is that a Biotechnology Project Manager oversees project planning, coordination, and execution within biotech companies, focusing on timelines and budgets. In contrast, a Research Scientist conducts experiments and develops new biotech products or knowledge. Both roles require strong biotech credentials, but their daily tasks and focus areas differ significantly.

What are the key skills and qualifications needed to thrive as a biotechnology project manager, and why are they important?

To thrive as a Biotechnology Project Manager, you need a solid background in biological sciences or engineering, project management expertise, and often an advanced degree such as an MSc or PhD. Familiarity with tools like Microsoft Project, Gantt charts, regulatory compliance systems, and certifications such as PMP are commonly required. Strong leadership, communication, and problem-solving skills set exceptional candidates apart in managing cross-functional teams and complex timelines. These skills and qualities are essential to effectively coordinate scientific projects, ensure regulatory compliance, and deliver successful outcomes in a dynamic biotech environment.

What are some common challenges faced by biotechnology project managers in cross-functional team environments?

Biotechnology Project Managers often work with multidisciplinary teams composed of scientists, regulatory specialists, manufacturing experts, and business development professionals. One common challenge is ensuring clear communication and alignment across these diverse groups, especially when technical jargon or differing priorities create misunderstandings. Additionally, managing project timelines in a highly regulated environment, where unexpected trial results or compliance issues may cause delays, requires strong adaptive planning. Successful Biotechnology Project Managers foster collaboration by setting clear goals, conducting regular check-ins, and proactively addressing potential roadblocks.
What are popular job titles related to Biotechnology Project Manager jobs in Santa Rosa, CA? For Biotechnology Project Manager jobs in Santa Rosa, CA, the most frequently searched job titles are:
What job categories do people searching Biotechnology Project Manager jobs in Santa Rosa, CA look for? The top searched job categories for Biotechnology Project Manager jobs in Santa Rosa, CA are:
What cities near Santa Rosa, CA are hiring for Biotechnology Project Manager jobs? Cities near Santa Rosa, CA with the most Biotechnology Project Manager job openings:
Infographic showing various Biotechnology Project Manager job openings in Santa Rosa, CA as of July 2026, with employment types broken down into 81% Full Time, 13% Part Time, 1% Temporary, 4% Contract, and 1% Summer. Highlights an 75% Physical, 3% Hybrid, and 22% Remote job distribution, with an average salary of $105,161 per year, or $50.6 per hour.

Sr. Project Manager, Global External Manufacturing

BIOMARIN PHARMACEUTICAL

Novato, CA • Hybrid

Full-time

Posted 14 days ago


BioMarin Pharmaceutical rating

7.8

Company rating: 7.8 out of 10

Based on 8 frontline employees who took The Breakroom Quiz

52nd of 86 rated pharmaceutical


Job description

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 - Novato, 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, andbenefits realization.
  • Establish and maintain project charters, RAID logs, decision logs, and governance artifacts to ensure transparent, consistent, and auditready oversight.
  • Ensure project scope, prioritization, and objectives remain aligned with strategic, operational, compliance, and capacity requirements across GEO.
  • Prepare and present concise, decisionfocused 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, executionready 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 endtoend 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 inspectionready 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 crossfunctional 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 handson use of modern project management, analytics, and AIenabled tools to independently build and maintain integrated schedules, model dependencies and critical paths, analyze delivery risk, and translate data into decisionready 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.

Employment Type: Fulltime-Regular

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