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Entry Level Biotech Project Management Jobs in Riverside, CA

Cryoport

Validation Engineer

Irvine, CA

Proficiency in Microsoft Office (Word, Excel, Power Point, Teams) Project Management skills ... ISO 21973 Biotechnology * General requirements for transportation of cells for therapeutic use ...

Cryoport, Inc.

Validation Engineer

Irvine, CA · On-site

... manage multiple projects within overlapping timeframes. • Team player with ability to manage ... ISO 21973 Biotechnology * General requirements for transportation of cells for therapeutic use ...

WINONICS

IT Support Specialist (Entry-Level)

Brea, CA · On-site

$20 - $23/hr

... equipment • Manage user accounts, password resets, permissions, and onboarding/offboarding ... special projects and provide general support to the IT team Qualifications • 0-2 years of ...

WINONICS

IT Support Specialist (Entry-Level)

Brea, CA · On-site

$20 - $23/hr

... equipment • Manage user accounts, password resets, permissions, and onboarding/offboarding ... special projects and provide general support to the IT team Qualifications • 0-2 years of ...

AECOM

Entry Level Structural Engineer

Orange, CA

... managers and other professionals delivering projects that create a positive and tangible impact ... AECOM is actively seeking a highly motivated Entry Level Structural Engineer to join our California ...

AECOM

Entry Level Structural Engineer

Orange, CA

... managers and other professionals delivering projects that create a positive and tangible impact ... AECOM is actively seeking a highly motivated Entry Level Structural Engineer to join our California ...

AECOM

Entry Level Structural Engineer

Orange, CA · On-site

... managers and other professionals delivering projects that create a positive and tangible impact ... AECOM is actively seeking a highly motivated Entry Level Structural Engineer to join our California ...

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All JobsEntry Level Biotech Project Management JobsEntry Level Biotech Project Management Jobs in Riverside, CA

Entry Level Biotech Project Management information

See Riverside, CA salary details

$34.4K

$85.6K

$157K

How much do entry level biotech project management jobs pay per year?

As of Jun 18, 2026, the average yearly pay for entry level biotech project management in Riverside, CA is $85,615.00, according to ZipRecruiter salary data. Most workers in this role earn between $69,900.00 and $92,300.00 per year, depending on experience, location, and employer.

What are some common challenges faced by entry-level biotech project managers, and how can they effectively navigate them?

Entry-level biotech project managers often face challenges such as coordinating cross-functional teams, managing shifting project priorities, and understanding complex scientific concepts. Navigating these challenges requires strong communication skills, a willingness to learn from experienced colleagues, and effective time management. Building relationships with both scientific and business stakeholders can help bridge knowledge gaps and ensure projects stay on track. Seeking mentorship within the organization and proactively asking questions can also accelerate growth and confidence in the role.

What are the key skills and qualifications needed to thrive as an Entry Level Biotech Project Manager, and why are they important?

To thrive as an Entry Level Biotech Project Manager, you need a solid background in biological sciences or biotechnology, strong organizational skills, and preferably a bachelor's degree in a related field. Familiarity with project management tools (like Microsoft Project or Asana) and understanding of regulatory compliance systems such as Good Laboratory Practices (GLP) are often required. Effective communication, teamwork, and adaptability are crucial soft skills for coordinating cross-functional teams and managing dynamic project timelines. These competencies ensure projects are executed efficiently, milestones are met, and team collaboration drives successful outcomes in a complex biotech environment.

What is the difference between Entry Level Biotech Project Management vs Entry Level Biotech Research Associate?

AspectEntry Level Biotech Project ManagementEntry Level Biotech Research Associate
Required CredentialsBachelor's in Life Sciences, Project Management knowledgeBachelor's in Biology, Biochemistry, or related field
Work EnvironmentCross-functional teams, project planning, coordinationLaboratory setting, experimental work, data collection
Employer & Industry UsageBiotech companies, pharma firms, research organizationsResearch labs, biotech firms, academic institutions
Common Search & ComparisonYesYes

Entry Level Biotech Project Management focuses on coordinating projects, timelines, and team communication within biotech companies, requiring some project management knowledge. In contrast, Entry Level Biotech Research Associate primarily involves conducting experiments and data analysis in laboratory settings. Both roles are common in biotech industries but serve different functions—one manages projects, the other conducts research.

What is entry level biotech project management?

Entry level biotech project management involves supporting the planning, coordination, and execution of projects within biotechnology organizations. Individuals in these roles typically assist senior project managers by tracking project milestones, organizing meetings, preparing documentation, and facilitating communication among team members. They help ensure that projects stay on schedule and within budget while gaining a foundational understanding of the biotech industry and project management processes. This role is ideal for recent graduates or professionals new to biotech, offering opportunities to develop essential skills for career growth.
What are popular job titles related to Entry Level Biotech Project Management jobs in Riverside, CA? For Entry Level Biotech Project Management jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Entry Level Biotech Project Management jobs in Riverside, CA look for? The top searched job categories for Entry Level Biotech Project Management jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Entry Level Biotech Project Management jobs? Cities near Riverside, CA with the most Entry Level Biotech Project Management job openings:
Entry Level Biotech Project Management jobs near you
Infographic showing various Entry Level Biotech Project Management job openings in Riverside, CA as of June 2026, with employment types broken down into 1% As Needed, 82% Full Time, 15% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $85,615 per year, or $41.2 per hour.

Validation Engineer

Cryoport

Irvine, CA

Full-time

Medical, Retirement

Posted 23 days ago

Job description

Cryoport Systems is the life science industry's most trusted provider of supply chain solutions for temperature-sensitive materials, serving biopharmaceutical, IVF and surrogacy and animal health organizations around the world. Cryoport Systems' proprietary Cryoport Expressshippers, CryoportalLogistics Management Platform, leading-edge SmartpakCondition Monitoring System and geo-sensing technology paired with unparalleled logistics expertise and 24/7/365 customer support, make Cryoport Systems the end-to-end temperature controlled supply chain partner that you can trust.

POSITION SUMMARY:

The Validation Engineer - Consulting Services will support the Consulting Services team's offerings around shipper, packaging, and shipping lane qualifications across temperature sensitive supply chains. This is a client-facing role within the Cryoport Systems Consulting Services department that is responsible for engaging in client discussions, performing qualifications, and developing technical reports.

PRIMARY RESPONSIBILITIES (include but are not limited to):

Participate and oversee internal Consulting Services qualification processes including:

  • Assist in the development of validation procedures.

  • Perform internal validations including developing validation protocols and reports, preparing equipment, and documenting & analyzing test results.

  • Support project creations for shipping lane qualifications, packaging configurations, systemized operational qualifications (physical and/or thermal performance testing), and shipping feasibility studies.

  • Manage qualification activities for Consulting Services' Consulting Services client related projects.

  • Work as a team with all Consulting Services team members.

  • Engage with clients presenting validation plans in client collaboration meetings.

  • Develop and customize customer centric quality driven protocols.

  • Assists with coordination between external third-party testing laboratories to ensure protocol execution, timelines, and quality metrics are achieved.

  • Evaluate, document, and articulate client specific results utilized strong communication skills.

  • Assist in optimizing existing protocols, processes, and reporting for all validation activities.

Engage in continuous process improvement areas within Cryoport Systems Consulting Services

Support cross-organizational departments as needed.

COMPETENCIES & PERSONAL ATTRIBUTES:

Professional with high attention to detail who focuses on client success.

Strong Communication Skills n written and verbal.

Analytical thinker with proficient skills in math, statistics, and data analysis applications

Strong organizational skills to manage multiple projects within overlapping timeframes.

Team player with ability to manage internal and external teams to achieve deliverables.

Self-motivated with initiative to self-learn to fill in knowledge gaps and expand contributions.

QUALIFICATIONS AND EDUCATION REQUIREMENTS:

BA/BS degree (in Life Sciences/Biopharma or a related healthcare field is highly preferred but not required)

2+ years of experience in Biopharmaceuticals, Medical Device Industry (specifically Cell & Gene Therapies is highly preferred)

2+ Years of Experience in writing professional documentation with customer-facing materials.

Preferred experience with ISO, IATA, ASTM and ISTA standards relating to the pharmaceutical supply chain.

Preferred experience with Equipment and Process Validation using DQ, IQ, OQ, and PQ.

Knowledge of cGMP requirements, FDA and ICH guidelines is highly preferred.

Experience using Excel, creating pivot tables, graphs and customer digestible and meaningful visual and tabular analytics.

Proficiency in Microsoft Office (Word, Excel, Power Point, Teams)

Project Management skills/ training is desirable.

PREFERRED SKILLS:

Understanding of:

  • Cold Chain and temperature-sensitive logistics.

  • Packaging testing and qualification.

  • (GDP) Good Distribution Practices.

  • USP 36 (Chapter 1079) Good Storage and Distribution Practices for Drug Products.

  • ISO 21973 Biotechnology

  • General requirements for transportation of cells for therapeutic use.

  • 21CFR Part 210 cGMP in Manufacturing, Processing, Packing, or Holding of Drugs.

  • 21CFR Part 211 cGMP for Finished Pharmaceuticals.

Compensation:Up to $120,000 depending on experience + bonus, stock, 401k match, benefits, etc.

Cryoport Systems is an Equal Opportunity Employer offering competitive compensation with a generous benefits package that includes health insurance, a 401K with company match and stock equity (Nasdaq: CYRX).

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