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Project Manager Biotech Jobs in Berkeley, CA (NOW HIRING)

Biotech Program Manager Location: South San Francisco Type: Full-time Ohalo is hiring a Biotech ... projects into a single coherent program plan. * Directly manage and drive execution of cross ...

Biotech Program Manager Location: South San Francisco Type: Full-time Ohalo is hiring a Biotech ... projects into a single coherent program plan. * Directly manage and drive execution of cross ...

Biotech Program Manager Location: South San Francisco Type: Full-time Ohalo is hiring a Biotech ... projects into a single coherent program plan. * Directly manage and drive execution of cross ...

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Project Manager Biotech information

See Berkeley, CA salary details

$26

$56

$93

How much do project manager biotech jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for project manager biotech in Berkeley, CA is $56.62, according to ZipRecruiter salary data. Most workers in this role earn between $49.13 and $62.12 per hour, depending on experience, location, and employer.

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?

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.

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 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.

What are popular job titles related to Project Manager Biotech jobs in Berkeley, CA?

For Project Manager Biotech jobs in Berkeley, CA, the most frequently searched job titles are:

What job categories do people searching Project Manager Biotech jobs in Berkeley, CA look for?

The top searched job categories for Project Manager Biotech jobs in Berkeley, CA are:

What cities near Berkeley, CA are hiring for Project Manager Biotech jobs?

Cities near Berkeley, CA with the most Project Manager Biotech job openings:

Infographic showing various Project Manager Biotech job openings in Berkeley, CA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 83% In-person, and 17% Remote job distribution, with an average salary of $117,772 per year, or $56.6 per hour.

Sr. Project Manager, Global External Manufacturing

BioMarin Pharmaceutical Inc.

Novato, CA • On-site

$120 - $180/hr

Other

Posted 28 days ago


BioMarin Pharmaceutical rating

7.8

Company rating: 7.8 out of 10

Based on 8 frontline employees who took The Breakroom Quiz

50th of 86 rated pharmaceutical


Job description

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 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 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.

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