21 CFR jobs in California

Project Manager/ Business Analyst (Clinical Operations)

Hybrid in Foster City, California

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Yesterday

Job Title: Project Manager/ Business Analyst (Clinical Operations) Location: Foster City, CA (Hybrid)Employment Type: Full-Time (FTE) Job SummarySeeking a Senior Project Manager / Business Analyst with strong Clinical Operations expertise and hands-on experience in Risk-Based Monitoring (RBM/RBQM). Responsible for requirements gathering, project delivery, stakeholder management, and implementation of clinical systems and monitoring processes. Key ResponsibilitiesLead requirements gathering for R

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Full-time

$160,000 - $160,000

GxP Project Manager (Pharma)

Hybrid in San Francisco, California

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9d ago

Job Title: GxP Project Manager Location: Bay Area, CA Duration: 6+ months with possible of extension Required Qualifications Bachelor's degree in Engineering, Computer Science, Life Sciences, Pharmacy, Biotechnology, or related field.8+ years of Project Management experience within the Pharmaceutical or Biotechnology industry.5+ years managing GxP-regulated projects.Strong understanding of GMP, GxP, GAMP 5, FDA regulations, and 21 CFR Part 11.Experience managing Computer System Validation (CSV)

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Contract, Third Party

$80 - $90

Validation Analyst

Hybrid in San Francisco, California

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Today

Role Overview Seeking an experienced Validation Analyst to support Roche's GIP program, focusing on validation of medical imaging applications, AI/ML workflows, and the Algorithm Workbench platform. The role will ensure system quality, regulatory compliance, data integrity, and end-to-end validation readiness. Key Responsibilities Develop and execute Computer System Validation (CSV) deliverables, including validation plans, risk assessments, IQ/OQ/PQ protocols, and validation summary reports.

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Full-time

60 - 70

Validation Analyst

Hybrid in San Francisco, California

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Today

Job Title: Validation AnalystProject: Medical Imaging & Algorithm Workbench Location: San Francisco, CA Work Model: Hybrid 4 Days Onsite Role OverviewWe are seeking an experienced Validation Analyst to support Roches GIP program, focusing on the validation of medical imaging applications, AI/ML workflows, and the Algorithm Workbench platform. The ideal candidate will ensure system quality, regulatory compliance, data integrity, and end-to-end validation readiness while supporting software rele

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Contract, Third Party

70 - 80

COMPONENT ENGINEER 3

Sunnyvale, California

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Yesterday

Description: Position Overview The Supplier Engineer is responsible for ensuring suppliers reliably support plant production by meeting Intuitive requirements for quality, delivery, capacity, cost, and service. This role is highly execution-focused and serves as the primary technical interface between the plant and suppliers to resolve line-impacting issues, improve supplier manufacturing processes, and maintain stable production operations across multiple product families. The Supplier

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Contract, Third Party

$60 - $75

Component Engineer 4

Sunnyvale, California

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Yesterday

Description: WOW: Minimum 3 Days onsite Job Title: Contingent Supplier Engineer MP Systems Department: Supplier Engineering Reports to: Sr Manager, Supplier Engineering Joining Intuitive Surgical means joining a team dedicated to using technology to benefit patients by improving surgical efficacy and decreasing surgical invasiveness, with patient safety as our highest priority. Primary Function of Position: The mission of Supplie

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Third Party, Contract

$93 - $93

Loftware Spectrum Technical Lead

Remote

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3d ago

Role : Loftware Spectrum Technical Lead / Solution Engineer Position Summary Responsible for the technical design, configuration, integration, support, and lifecycle management of Integer's Loftware Spectrum enterprise labeling platform. This role serves as the primary technical resource between Labeling COE, SAP, Oracle, manufacturing sites, Quality, and implementation partners to ensure a scalable, compliant, and supportable global labeling solution. The individual will lead architecture, busi

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Contract, Third Party

Depends on Experience

Business Systems Support Analyst

Laguna Beach, California

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8d ago

HonorVet Technologiesis a Service Disable Veteran-Owned IT staffing firm, ISO 9001, and ISO 27001 certified, working with federal agencies, state governments, and Fortune 500 enterprise clients across the US. What makes us different isn't a tagline; it's the way we work. We don't forward resumes and hope for the best. We take the time to understand where a professional like you are headed and only reach out when we genuinely believe there's a fit worth exploring. I came across your profile, and

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Contract

$26 - $33.85

Technical Program Manager

Bell Gardens, California

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28d ago

Payrate: $90.00 - $100.00/hr. Responsibilities:Release Program Leadership:Manage deliverables to completion for Companys FDA approved Hearing Correction feature - software as medical device (SaMD) in accordance with Quality Management System (QMS) software release process end-to-end: define release scope, schedule, and milestones.Maintain a single source of truth for release status, dependencies, risks, and open items across all functions.Cross-Functional Coordination:Coordinate release activit

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Contract, Third Party

$90 - $100

Sr. Computer Systems Validation Analyst

Foster, California

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14d ago

Summary : We are seeking a Senior Computer Systems Validation (CSV) Analyst with strong experience in GxP-regulated pharmaceutical/life sciences environments. The candidate will be responsible for planning, leading, and executing validation activities for SCADA, Rockwell FactoryTalk, PLCs, and Ignition process control systems. The role requires hands-on expertise in GAMP 5, 21 CFR Part 11, EU Annex 11, validation lifecycle documentation, risk assessments, change controls, and qualification pro

Full-time

Sr. Computer Systems Validation Analyst

Foster City, California

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14d ago

Full-time

SAP Validation

Remote

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23d ago

Job Title: SAP Validation Life Sciences & Pharmaceuticals Location: Remote Duration : Long term ONLY SAP VALIDATION PROFILES Required Qualifications Bachelor s degree in computer science, Information Technology, Engineering, Life Sciences, or related field. 8+ years of experience in SAP validation or Computer System Validation (CSV). GxP regulations 21 CFR Part 11 Annex 11 GAMP 5 Experience with validation tools and documentation management systems. Familiarity with change management and deviat

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Contract

Depends on Experience

CSA/CSV Validation Consultant

Remote or Arlington, Virginia

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Yesterday

Role - CSA/CSV Validation Consultant Remote Skills & Experience Required: empower or similar HPLC software Deep expertise in validating GxP-regulated IT systems within the Pharma/Life Sciences domain Familiarity with QMS processes including deviation management, CAPA, and change control. Strong command of CSA (Computer Software Assurance) principles Solid knowledge with 21 CFR Part 11, Annex 11, ISPE AI guidance, GxP data integrity principles (ALCOA+). Proven ability to write and manage valida

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Contract

PLM Windchill Solution Architect/ SME

Remote

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Today

Position SummaryWe are seeking a highly experienced Windchill PLM Subject Matter Expert to assess the current PTC Windchill environment and develop a strategic upgrade roadmap for Windchill 2027. The ideal candidate will have strong technical and functional expertise in Windchill, PLM transformation, system upgrades, data migration, and integrations within regulated industries, preferably Medical Devices. Key ResponsibilitiesAssess the existing Windchill environment, including configurations, cu

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Contract, Third Party

Depends on Experience

Computer System Validation Engineer

San Diego, California

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14d ago

Job Summary: We are seeking a motivated and detail-oriented Computer System Validation (CSV) Engineer with 1-2 years of experience to support validation and compliance activities within the Pharmaceutical and Medical Devic e industries. The ideal candidate will assist with the validation of computerized systems in regulated GxP environments and ensure systems comply with applicable regulatory and quality requirements. The candidate should have a strong understanding of validation principles, doc

Full-time

LIMS Developer-Analyst

Thousand Oaks, California

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Today

LabWare LIMS Developer (Contract-to-Hire) Location: Hybrid (Thousand Oaks, CA - 3 days/week preferred) or Remote with 10-25% travel We are seeking an experienced LabWare LIMS v7 Developer to support and enhance laboratory systems in a regulated GxP environment. This role will be responsible for LIMS development, system integrations, L2/L3 support, validation documentation, and ongoing operational support across multiple Life Sciences sites. Key Responsibilities Design, configure, and support

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Contract

$61 - $80

Salesforce Marketing Cloud Technical Consultant / Lead

Alameda, California

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Yesterday

Position: Salesforce Marketing Cloud Technical Consultant / Lead Location: Alameda, CA (Onsite) Duration: 06 Months (Extendable) 4-8 years of experience. Salesforce Marketing Cloud, CRM platforms. Must have: Experience supporting campaign execution, platform optimization, integrations, and reporting. Fully involved in Marketing Function, skilled in Marketing Cloud Development as well. Must Report to Client Alameda, California Office Role Descriptions: Strong working knowledge of Sales Cloud

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Contract, Third Party

50 - 60

PLM Windchill Solution Architect/ SME

Remote

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Yesterday

Role : PLM Windchill Solution Architect/ SME Location : Remote Type : Contract Required Skills & Experience Windchill Expertise 12+ years of hands-on experience with PTC Windchill. Expertise across: Windchill PDMLink ProjectLink MPMLink PartsLink Change Management Document Management Configuration Management Strong knowledge of Windchill versions 12.x/13.x and roadmap toward Windchill 2027. Experience with Windchill upgrades, migrations, and modernization programs. Technical Skills

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Contract, Third Party

Depends on Experience

Product Owner

Remote

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9d ago

Role OverviewThe Product Owner for the Clinical Trial Platform is responsible for defining the product vision, strategy, and roadmap for technology that supports end to end clinical trial execution.This role blends product management discipline with deep understanding of regulated clinical workflows, ensuring the platform delivers measurable value to sponsors, CROs, research sites, and patients. The PM drives feature development across study startup, patient identification, eligibility, randomiz

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Contract, Third Party

$80 - $85

Computer Vision Engineer

Remote

•

Yesterday

Role: Computer Vision EngineerLocation: Remote with travel required 50%Duration: 6months with possible extensionRole OverviewWe are seeking a Computer Vision Engineer to own the development and integration of real-time automated visual inspection systems for our pharmaceutical packaging lines. In this role, you will design and deploy edge-based vision models that interface with high-speed cameras and IoT hardware to detect packaging defects, verify serialization, and ensure 100% quality complian

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Contract

Depends on Experience

21 CFR jobs in California, USA