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Biotechnology Project Manager Jobs in Riverside, CA

Avid Bioservices

Project Manager

Tustin, CA · On-site

$99K - $124K/yr

Bachelor's degree in a scientific discipline. * 3+ years of experience in biotechnology or pharmaceuticals with specific project management capacity. * Project Management certification is ...

New

Avid Bioservices

Project Manager - CMC

Tustin, CA

$99K - $124K/yr

Bachelor's degree in a scientific discipline. * 3+ years of experience in biotechnology or pharmaceuticals with specific project management capacity. * Project Management certification is ...

New

Crane Company

Project Engineer

Jurupa Valley, CA · On-site

$81K - $110K/yr

Time management - Ability to prioritize tasks and manage multiple projects. Interpersonal Skills ... Among the industries served are the chemical processing, biotechnology, pharmaceutical, oil & gas ...

Crane Company

Project Engineer

Jurupa Valley, CA · Hybrid

$81K - $110K/yr

Time management - Ability to prioritize tasks and manage multiple projects. Interpersonal Skills ... Among the industries served are the chemical processing, biotechnology, pharmaceutical, oil & gas ...

PSG

Engineering Manager

Grand Terrace, CA · On-site

$138K - $152K/yr

Ensures new product development projects are successfully completed on time * Ensures product ... Biotech, Quantex™, Quattroflow ® , and Wilden ® . PSG products are manufactured on three ...

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All JobsBiotechnology Project JobsBiotechnology Project Manager JobsBiotechnology Project Manager Jobs in Riverside, CA

Biotechnology Project Manager information

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$48

$79

How much do biotechnology project manager jobs pay per hour?

As of Jul 9, 2026, the average hourly pay for biotechnology project manager in Riverside, CA is $48.24, according to ZipRecruiter salary data. Most workers in this role earn between $41.88 and $52.93 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 Riverside, CA? For Biotechnology Project Manager jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Biotechnology Project Manager jobs in Riverside, CA look for? The top searched job categories for Biotechnology Project Manager jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Biotechnology Project Manager jobs? Cities near Riverside, CA with the most Biotechnology Project Manager job openings:
Biotechnology Project Manager jobs near you
Project Manager

Project Manager

Avid Bioservices

Tustin, CA • On-site

$99K - $124K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 3 days ago

New

Job description

Description
Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.
Your Role:
Join forces with our dynamic project management team and ignite your passion for driving impactful client projects! As a Project Manager, you'll lead the coordination and planning of cross-functional activities for designated projects, ensuring they not only meet but exceed their objectives within set timelines and budget constraints.
Your journey with us will involve diving deep into client relationships, seamlessly onboarding projects, crafting efficient processes, facilitating smooth technology transfers, and orchestrating GMP operations within the thrilling realm of Drug Substance and Viral Vector space.
If you're ready to roll up your sleeves and be a driving force behind transformative projects, then seize this opportunity to make your mark in a team that thrives on innovation and collaboration!
  • Manage early stage and/or late-stage biologics projects to drive deliverables and maintain budget.
  • Support the project management team implementation of standardized templates, project governance, project process flow, and resource allocation tools and techniques.
  • Supports the planning/preparation/facilitation of internal and client facing meetings (technology transfer, process development, manufacturing, and quality).
  • Supports project readiness activities related to biologics projects including early-stage and late-stage covering process validation and commercialization (timeline generation, documentation tracking, schedule adherence, functional resource planning, risk assessment, and budgeting).
  • Supports project interface with operations/outside contractor/supply chain for GMP production readiness, schedules and facilitate sub-team (as assigned) meetings.
  • Provides Project Management support to all assigned projects including oversight of project charter, project plan/timeline, risk management and risk elevation, project monitoring, and project closure.
  • Responsible for effective meeting facilitation, maintenance of meeting minutes, and action item generation, follow-up, and elevation for all assigned projects.
  • Supports the high-level management of corporate initiatives.
  • Back up for Sr. Project Management activities.
  • Other tasks may be assigned as needed.

Minimum Qualifications:
  • Bachelor's degree in a scientific discipline.
  • 3+ years of experience in biotechnology or pharmaceuticals with specific project management capacity.
  • Project Management certification is advantageous.
  • Proficiency in MS Project is essential.
  • Strong attention to detail and ability to multitask effectively.
  • Familiarity with the drug development process.
  • Excellent written and oral communication skills.
  • Occasional overnight travel by land and/or air may be required to attend seminars, conferences, or client meetings.

Position Type/Expected Hours of Work:
This role is a full-time position. Days of work are Monday through Friday.
Compensation:
We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.
The compensation range for this role is $99,200 - $124,000 annually, depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
Who you are:
  • You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
  • Your written and verbal skills are out of this world, and you communicate with clarity and confidence.
  • You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.
  • You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.

Physical Demands & Work Environment:
In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.

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