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Project Manager Biotech Jobs in Santa Rosa, CA (NOW HIRING)

Kelly Services

Manufacturing Associate

Novato, CA

$28 - $32.20/hr

Prefers 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 ...

SC Builders Inc

Estimator

Bodega Bay, CA · On-site

Cool projects. Awesome people. At SC Builders we have a passion to build for our clients, our ... Commercial experience to include core/shell office buildings or similar, office TIs, biotech and ...

SC Builders

Estimator

Bodega Bay, CA · On-site

$145K - $200K/yr

Cool projects. Awesome people. At SC Builders we have a passion to build - for our clients, our ... Commercial experience to include core/shell office buildings or similar, office TI's, biotech and ...

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All JobsProject Manager Biotech JobsProject Manager Biotech Jobs in Santa Rosa, CA

Project Manager Biotech information

See Santa Rosa, CA salary details

$23

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$83

How much do project manager biotech jobs pay per hour?

As of Jun 25, 2026, the average hourly pay for project manager biotech 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 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.

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 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, and why are they important?

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.
What are popular job titles related to Project Manager Biotech jobs in Santa Rosa, CA? For Project Manager Biotech jobs in Santa Rosa, CA, the most frequently searched job titles are:
What job categories do people searching Project Manager Biotech jobs in Santa Rosa, CA look for? The top searched job categories for Project Manager Biotech jobs in Santa Rosa, CA are:
What cities near Santa Rosa, CA are hiring for Project Manager Biotech jobs? Cities near Santa Rosa, CA with the most Project Manager Biotech job openings:
Project Manager Biotech jobs near you
Senior CQV Specialist (Client site based - Novato, CA)

Senior CQV Specialist (Client site based - Novato, CA)

Wood Plc

Novato, CA • On-site

Other

Posted 28 days ago

Job description

Overview / Responsibilities

Wood PLC, on a global scale, serves the Pharma-Bio, Oil & Gas, Federal, Infrastructure, Manufacturing, Mining, and Power Industries. Our Philadelphia office has become the center of excellence for our global Life Sciences network. It provides process engineering, process design, and commissioning - qualification - validation (CQV) services to pharmaceutical/biotechnology clients worldwide. For projects of every scale, we provide services that support a facility's entire life cycle to bring life-saving therapeutics from concept through fruition. Learning from our team of industry-leading experts in facility design, regulatory standards, and project management will pay dividends toward your future engineering career.

Our CQV group at Wood is growing and we are adding to our well respected and established team of Senior CQV Specialists. We are looking for candidates experienced in commissioning, qualification and/or validation within the pharmaceuticals, biopharmaceuticals, vaccines, and aseptic processing areas. If you are interested in working with a global leader in life sciences and possess the skill and drive to flourish in a dynamic and exciting environment, apply today!

****This position offers a competitive salary, opportunty for growth, and a signing bonus.

Key Responsibilities

  • Preparation and execution of CQV life cycle deliverables, URS/DR/DQ/Risk Assessments/CTP/FAT/SAT/IOQ/PQ/PV/TOPs/Final reports
  • Ability to work independently and direct the work of junior team members
  • Ability to read, review and perform walk downs of P&IDs
  • Manage punch list and execute deviation resolution
  • Effectively interfacing and communicating with 3rd parties, client and CQV project teams
  • Ability to multi-task and adjust priorities to meet aggressive project timelines.
  • Use of test equipment, as required.
  • Complete work at client sites, the ability to travel 100% of the time is essential.
  • Ability to complete work remotely, as required.
Skills / Qualifications

Skills/Qualifications

  • Degree in engineering (preferably) or life sciences or suitable industry experience.
  • Minimum of 5 years of direct experience in CQV and/or Engineering.
  • Strong and clear communication skills, both written and verbal.
  • Ability to effectively interface with Wood management, co-workers, clients, vendors and subcontractors.
  • Understanding with advanced knowledge of common unit operations and processes used in biopharma/pharmaceutical manufacturing.
  • Thorough knowledge of cGMPs as related to the pharmaceutical industry.
  • Strong computer skills.
  • Customer service oriented.
  • Ability to understand while manage project scope and schedule with drive to achieve both.
  • Ability to work safely and keep the safety of those around in mind.
  • Ability to recognize hazards and communicate these to the appropriate individuals.

Physical Requirements

  • While performing the duties of this job, the employee is frequently required to walk, crouch, sit, and stand and may require close vision work
  • Ability to work at an active construction site is required
Company Overview

Wood is a global leader in engineering and consultancy across energy and the built environment, helping to unlock solutions to some of the world's most critical challenges. We provide consulting, projects and operations solutions in more than 60 countries, employing around 40,000 people. www.woodplc.com

Diversity Statement

We are an equal opportunity employer that recognises the value of a diverse workforce. All suitably qualified applicants will receive consideration for employment on the basis of objective criteria and without regard to the following (which is a non-exhaustive list): race, colour, age, religion, gender, national origin, disability, sexual orientation, gender identity, protected veteran status, or other characteristics in accordance with the relevant governing laws.

Employment Type: OTHER

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