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Biotechnology Project Manager Jobs in Riverside, CA

The Remas Company, LLC

Project Manager

La Verne, CA

Should know GxP, Validation and possibly MES GxP Documentation is must Seeking a Project Manager with experience in Pharma/ Biotech/ Life Sciences/ Medical Device/ Healthcare or Manufacturing a must ...

Avid Bioservices

Project Manager - CMC

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 ...

Avid Bioservices

Project Manager - CMC

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 ...

Avid Bioservices

Project Manager - CMC

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 ...

Avid Bioservices

Project Manager - CMC

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 ...

Astrix Inc

IT Project Manager (part-time)

Tustin, CA · On-site

$55 - $57/hr

Manage IT projects from planning through implementation and completion. * Develop project plans ... Experience in biotech, life sciences, healthcare, or a regulated environment is a plus. * PMP, CAPM ...

Fujifilm

Sr. IT Project Manager

Irvine, CA · On-site

$126K - $145K/yr

The Senior IT Project Manager will direct large, complex IT programs and oversee portfolio ... biotech and pharma to tackle the world's biggest health challenges. Imagine being part of a team ...

Spyglass Pharma

R&D Project Manager

Irvine, CA · On-site

... biotechnology, or medical device R&D including experience supporting cross-functional projects or ... Demonstrated ability to manage multiple priorities andidentifydependencies across workstreams in a ...

Spyglass Pharma

R&D Project Manager

Irvine, CA · On-site

$95K - $110K/yr

... biotechnology, or medical device R&D including experience supporting cross-functional projects or ... Demonstrated ability to manage multiple priorities and identify dependencies across workstreams in ...

Evermont Group

Project Engineer

Anaheim, CA · On-site

$70K - $80K/yr

... biotech and other institutional clients across Southern California. It has built a strong base of ... Manage RFIs, submittals, change documentation and project records * Coordinate with subcontractors ...

Concuir, Inc

Project Engineer II to III

Irvine, CA · On-site

$90K - $110K/yr

... biotech manufacturing clients. In this role, you will quickly learn common client practices ... management and cGxP best practices to drive your overall success. Projects range from design ...

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

Biotechnology Project Manager information

See Riverside, CA salary details

$22

$48

$79

How much do biotechnology project manager jobs pay per hour?

As of Sep 10, 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 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 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 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
Infographic showing various Biotechnology Project Manager job openings in Riverside, CA as of August 2026, with employment types broken down into 86% Full Time, 13% Part Time, and 1% Contract. Highlights an 84% Physical, 2% Hybrid, and 14% Remote job distribution, with an average salary of $100,346 per year, or $48.2 per hour.

Project Manager

La Verne, CA

The Remas Company, LLC
See more jobs at The Remas Company, LLCexternal

Full-time

Re-posted 24 days ago

Job description

Should know GxP, Validation and possibly MES

GxP Documentation is must

Seeking a Project Manager with experience in Pharma/ Biotech/ Life Sciences/ Medical Device/ Healthcare or Manufacturing a must (Okay with either industry)

Responsibility:

  • This position is responsible for leading and performing activities in support of creating and maintaining GxP (GMP, GCP, and GLP) quality and compliance environment for SAP S/4 HANA. This position is also responsible for monitoring Computer System validation (CSV) as well as compliance with GxP regulations and 21 CFR Part 11.
  • Leads the effort to manage, and/or maintains validation of SAP S/4 HANA system.
  • Perform GxP and 21 CFR part 11 assessments and develop validation plan.
  • Develop functional risk strategy and perform functional risk assessment.
  • Review user business process documents and user requirements specification.
  • Review functional, technical and configuration design documents.
  • Prepare and/or review Configuration Qualification (CQ), Data Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ) and performance Qualification (PQ) protocols.
  • Review the test scripts for the requirements and test scenario coverage.
  • Lead overall protocol executions, log and track defects.
  • Review the executed test reports for the proper documentation of test results and evidence.
  • Review the defects for proper documentation per the checklist.
  • Prepare and maintain the traceability matrix to ensure all the requirements are covered in design documents and tested.
  • Prepare and approve qualification summary report.
  • Participates in Corrective and Preventive Action (CAPA), Maintains quality metrics.
  • Maintain overall project and issue tracker and report routinely.
  • Support release management activities by reviewing and ensuring the pre-requisites are completed prior to the release.
  • Review Quality System support documentation including Standard Operating Procedures (SOP), Work Instructions (WI) and training materials.
  • Maintain day to day activities status tracker and report routinely.
  • Lead the team of validation engineers located in different time zones.

Skills:

  • Excellent communication (oral and written) and attention to detail.
  • 8+ years in Computer System Validation in Life Science domain with minimum 3+ years of experience in managing large global SAP validation projects.
  • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude.
  • Excellent knowledge of GxP regulations, FDA and EMEA (European Medicines Evaluation Agency ) guidelines including 21 CFR Part 11.
  • Excellent knowledge of computer system validation and GAMP -5 standards.

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