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

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

$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

$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 ...

Fujifilm

Sr. IT Project Manager

Irvine, CA

$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 ...

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 ...

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 ...

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 ...

Posted today

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 ...

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All JobsProject Biotech JobsProject Manager Biotech JobsProject Manager Biotech Jobs in Riverside, CA

Project Manager Biotech information

See Riverside, CA salary details

$22

$48

$79

How much do project manager biotech jobs pay per hour?

As of Aug 5, 2026, the average hourly pay for project manager biotech 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 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?

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 Riverside, CA? For Project Manager Biotech jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Project Manager Biotech jobs in Riverside, CA look for? The top searched job categories for Project Manager Biotech jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Project Manager Biotech jobs? Cities near Riverside, CA with the most Project Manager Biotech job openings:
Project Manager Biotech jobs near you
Infographic showing various Project Manager Biotech job openings in Riverside, CA as of July 2026, with employment types broken down into 2% As Needed, 90% Full Time, 1% Part Time, 1% Temporary, 5% Contract, and 1% Summer. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution, with an average salary of $100,346 per year, or $48.2 per hour.

Project Manager

The Remas Company, LLC

La Verne, CA

Full-time

Posted 19 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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