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Science Program Manager Jobs in Oxnard, CA (NOW HIRING)

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Compliance Program Coordinator Pay rate: $25.00/hr Location: Carpinteria, CA, 93013 Shift: Mon ... manage multiple priorities Manufacturing, chemical, life sciences, medical device, or regulated ...

MAXIMO PROJECT MANAGER

Ventura, CA · On-site

$125K - $145K/yr

Bachelor's degree in Business, Information Systems, Computer Science, Engineering, Project Management, or related field. ● Experience: 2-4 years of Government program experience, preferably ...

Data Engineer

Camarillo, CA · On-site

$116K - $140K/yr

KBR's work is at the forefront of engineering, logistics, operations, science, program management, mission IT and cybersecurity solutions. * Collaborative Environment: Be part of a dynamic team that ...

Data Engineer

Camarillo, CA

$116K - $140K/yr

KBR's work is at the forefront of engineering, logistics, operations, science, program management, mission IT and cybersecurity solutions. * Collaborative Environment: Be part of a dynamic team that ...

Data Engineer with Security Clearance

Camarillo, CA · On-site

$116K - $140K/yr

KBR's work is at the forefront of engineering, logistics, operations, science, program management, mission IT and cybersecurity solutions. * Collaborative Environment: Be part of a dynamic team that ...

Naval Architect

Ventura, CA · On-site

$100K - $120K/yr

Support Program Manager with aligning schedules and workload assignments to handle concurrent ... Must have proven ability to interact with scientific and other technical personnel who may not be ...

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Science Program Manager information

See Oxnard, CA salary details

$40.8K

$113.8K

$166.3K

How much do science program manager jobs pay per year?

As of Jun 26, 2026, the average yearly pay for science program manager in Oxnard, CA is $113,798.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,200.00 and $140,300.00 per year, depending on experience, location, and employer.

What is the difference between Science Program Manager vs Research Scientist?

AspectScience Program ManagerResearch Scientist
CredentialsBachelor's or Master's in Science, project management certifications often preferredAdvanced degree (Master's or PhD) in a scientific field
Work EnvironmentProject coordination, cross-functional teams, administrative tasksLaboratory research, data analysis, experimental work
Employer & IndustryResearch institutions, biotech, pharma, government agenciesUniversities, research labs, industry R&D
Search & Comparison IntentUnderstanding project management roles in scienceScientific research and experimental work

The main difference is that a Science Program Manager oversees scientific projects, coordinating teams and resources, while a Research Scientist conducts experiments and generates scientific data. Both roles require strong scientific credentials, but their daily tasks and focus differ significantly.

What does a Science Program Manager do?

A Science Program Manager oversees the planning, coordination, and execution of scientific projects and programs. They work closely with research teams, stakeholders, and funding agencies to ensure that projects meet their objectives, stay within budget, and adhere to timelines. Their responsibilities often include grant management, facilitating communication between different departments, and ensuring compliance with regulatory standards. Science Program Managers play a key role in translating scientific goals into actionable plans and helping organizations achieve their research and development objectives.

What are the key skills and qualifications needed to thrive as a Science Program Manager, and why are they important?

To excel as a Science Program Manager, you need a strong background in scientific research or project management, typically supported by an advanced degree in a scientific field. Familiarity with project management tools (e.g., Microsoft Project, Asana) and certification such as PMP can be highly valuable. Excellent communication, leadership, and organizational skills are crucial for managing teams and coordinating across departments. These skills ensure effective alignment of scientific objectives, timely project delivery, and successful collaboration among stakeholders.

How does a Science Program Manager typically collaborate with researchers and cross-functional teams?

Science Program Managers play a crucial role in connecting researchers with other departments such as engineering, product development, and regulatory affairs. They coordinate project timelines, facilitate communication among stakeholders, and help resolve scientific or logistical challenges that arise during research initiatives. Regular meetings, status updates, and collaborative planning sessions are typical, allowing the Program Manager to ensure that projects remain aligned with broader organizational goals while supporting the innovative work of research teams.
What job categories do people searching Science Program Manager jobs in Oxnard, CA look for? The top searched job categories for Science Program Manager jobs in Oxnard, CA are:
What cities near Oxnard, CA are hiring for Science Program Manager jobs? Cities near Oxnard, CA with the most Science Program Manager job openings:

Validation Lifecycle & Periodic Review Program Manager

Validation & Engineering Group, Inc

Thousand Oaks, CA • On-site

Full-time

Posted 7 days ago


Job description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

  • Validation Lifecycle & Periodic Review Program Manager

Position Summary

We are seeking an experienced Validation Lifecycle & Periodic Review Program Manager to support our client in maintaining validated systems throughout their lifecycle. This role is responsible for managing validation lifecycle and periodic review programs for GMP equipment, facilities, utilities, controlled temperature chambers, computerized systems, and associated validation maintenance activities.

In addition to providing program leadership and client interface responsibilities, the successful candidate will be expected to actively support execution activities as needed, including review assessments, technical evaluations, report generation, and other validation lifecycle deliverables.

Responsibilities

  • Serve as the primary client interface for validation lifecycle and periodic review programs.
  • Develop and manage execution plans, schedules, staffing plans, and resource forecasts.
  • Lead program meetings, status updates, and performance reviews.
  • Monitor program metrics and key performance indicators.
  • Ensure timely execution and completion of review activities and deliverables.
  • Oversee the quality and consistency of validation lifecycle and periodic review documentation.
  • Support development, maintenance, and periodic updates of Validation Master Plans (VMPs).
  • Support Annual Product Review (APR) activities and associated summary reporting.
  • Coordinate activities across equipment, facility, utility, controlled temperature chamber, and computerized system workstreams.
  • Identify risks, issues, and resource constraints and develop mitigation strategies.
  • Provide technical leadership and mentorship to project team members.
  • Ensure compliance with GMP requirements, client procedures, and internal quality standards.
  • Perform and support validation lifecycle and periodic review activities as needed to support program objectives, resource demands, and critical deliverables.

Required Qualifications

  • Bachelor's degree in Engineering, Life Sciences, Quality, Computer Science, or a related technical discipline.
  • Minimum 8 years of experience within pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.
  • Minimum 3 years of experience leading validation, quality, compliance, engineering, or lifecycle management programs.
  • Strong knowledge of GMP regulations and validation lifecycle principles.
  • Experience managing multidisciplinary technical teams.
  • Excellent written and verbal communication skills.
  • Strong organizational, planning, and leadership abilities.

Preferred Qualifications

Experience supporting one or more of the following:

  • Equipment Periodic Reviews (EQPR)
  • Controlled Temperature Chamber Reviews (CTCPR)
  • Computerized System Periodic Reviews (CSPR)
  • Annual Audit Trail Reviews (AATR)
  • Validation Master Plans (VMP)
  • Annual Product Review (APR) support
  • Data Integrity Assessments
  • Change Control and Deviation Management
  • Maximo, TrackWise, Kneat, CDOCS, ServiceNow, or similar systems

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.