GMP jobs in California

Validation engineer with GMP QA validation

Remote

•

Yesterday

Hi, Greetings of the day!! Validation Enigneer with QA Remote Expert in testing, validation and compliance. - Min 5 Yrs Experience in GMP validation of QA analytics applications. - Min 3 Experience on using Tricentis qTest, Vera, and JIRA - Technical background in Full Stack technology for both front-end and back-end - Strong experience with data visualizations technology such as React, Angular, Javascript - Strong understanding of GxP and regulatory standards in pharmaceutical industry. - Exc

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Contract, Third Party

Depends on Experience

GMP/GDP QC Analyst (ONSITE)

Carpinteria, California

•

Today

Please note that this is a 12 to 18-month contract position. Qualifications: Some course work related to biochemistry, IHC or other related education is required. Bachelors, Masters or other University degree in a related field is highly preferred; Relevant experience or coursework including testing and the use and operation of laboratory equipment preferred. Computer skills including the use of Microsoft office suite and understanding of ERP system mechanics. Ability to multi-task with solid t

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Contract

Depends on Experience

Lead Validation Analyst ( Gxp,Gmp)

Remote

•

11d ago

Lead Validation Analyst ( Gxp/Gmp) Remote 12+Months Contract Mandatory Skills: GMP/GXP Job Summary: We are seeking an experienced Validation Lead to oversee and lead validation activities in compliance with GMP (Good Manufacturing Practice) and GxP (Good Clinical/ Laboratory Practice) regulations. The ideal candidate will have a strong background in managing validation processes for systems, equipment, and processes within regulated environments, ensuring compliance, quality, and safety standard

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Third Party, Contract

Depends on Experience

GMP Tester / Validation Engineer

Vacaville, California

•

Today

Job Description: We are seeking a skilled GMP Tester / Validation Engineer with strong experience in testing and validating applications in regulated environments (GMP, GxP, Pharma, Life Sciences). The ideal candidate will have hands-on expertise in validation testing, documentation, and compliance for critical applications such as MES, LIMS, ArchestrA, and manufacturing systems. This role requires a detail-oriented professional who can design and execute validation tests, review traceability ma

Full-time

Urgent Need for QUA015_Digital Quality Full Stack Developer (FE) - Mongo DB, Data analytics, Visualization, Dashboard-US

Remote

•

3d ago

Application/Process Sherlock, MIR/SIR, LIR, CAPA, Complaints Portals, SCAR and Change Management Dashboard, Incident Board, CAPA Board 10 solutions/design and visualization expert Role Description Full-stack web application developer with exceptional programming skills, proficient in both the front-end (user-facing parts of a website or application) and the back-end (server, database, and application logic) - Advanced skills in Data Analytics, Visualization, and Dashboard development - Strong

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Contract

Depends on Experience

Urgent Need for Test Engineer - Pharma Compliance(No H1b)

Remote

•

2d ago

Expert in testing, validation and compliance.- Min 5 Yrs Experience in GMP validation of QA analytics applications.- Min 3 Experience on using Tricentis qTest, Vera, and JIRA- Technical background in Full Stack technology for both front-end and back-end- Strong experience with data visualizations technology such as React, Angular, Javascript- Strong understanding of GxP and regulatory standards in pharmaceutical industry.- Excellent documentation and communication skills.

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Contract

Depends on Experience

Sr Engineer Process

California

•

Today

Job Description Dar seguimiento a problemas de calidad relacin con Almacn y Produccion.Gestionar No Conformidades (NCs) y acciones correctivas/preventivas (CAPA).Coordinar liberacin de material y producto en almacn bajo estndares regulatorios.Liderar y soportar auditoras internas, externas y de clientes.Implementar y dar seguimiento a indicadores de calidad en procesos de almacn y distribucin.Colaborar con equipos multifuncionales (produccin, logstica, compras, proveedores).Ingeniera Industrial

Full-time

Test Engineer - Pharma Compliance (Life sciences exp)

Remote

•

Today

Test Engineer - Pharma Compliance (Life sciences exp is required) Expert in testing, validation and compliance. - Min 5 Yrs Experience in GMP validation of QA analytics applications. - Min 3 Experience on using Tricentis qTest, Vera, and JIRA - Technical background in Full Stack technology for both front-end and back-end - Strong experience with data visualizations technology such as React, Angular, Javascript - Strong understanding of GxP and regulatory standards in pharmaceutical industry. -

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Third Party, Contract

$40,000 - $46

Manufacturing Engineer (Medical Device)

Los Angeles, California

•

21d ago

Description: What manufacturing methodologies are most commonly used here (e.g., lean, Six Sigma, GMP)? All of them Is medical device experience required or desired? Class 3 medical device experience is must What are the must-have vs. nice-to-have qualifications (education, certifications, years of experience)? Minimum 5-6 years of experience in supporting Manufacturing Engineering in class 3 medical device Knowledge of Process validation (IQ/OQ/PQ); Risk assessment; process controls Experience

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Third Party, Contract

Depends on Experience

SAP Tosca Functional

Foster City, California

•

8d ago

SAP Tosca Functional Consultant Foster City, CA (Onsite) (W2/C2C) Functional Role Only must have hands-on Tosca automation experience Industry Experience Required: Pharma / Life Sciences / Medical Device Manufacturing Core Skills: 10+ years in SAP SQA with strong functional expertise 5+ years hands-on Tricentis Tosca automation for SAP Deep knowledge of multiple SAP modules (OTC, P2P, MM, FI/CO, S/4, ECC, etc.) Strong experience in SAP upgrades, business-facing roles, and regulatory complianc

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Contract

Depends on Experience

Full Stack Developer- Mongo DB, Data analytics, Visualization, Dashboard

Remote

•

Today

We're seeking for a Full Stack Developer for our direct client. Please review the below job Description and revert with your interest for the same. Job details: Role: Full Stack Developer- Mongo DB, Data analytics, Visualization, Dashboard REMOTE Duration: 6 to 12 months Application/Process : Sherlock, MIR/SIR, LIR, CAPA, Complaints Portals, SCAR and Change Management Dashboard, Incident Board, CAPA Board Role Description Full-stack web application developer with exceptional programming skills,

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Contract

Depends on Experience

SAP Functional Consultant Pharma / Manufacturing / Supply Chain

Foster City, California

•

3d ago

SAP Functional Consultant Pharma / Manufacturing / Supply Chain Location: Foster City CA (Only Locals) C2C/W2 Key Requirements: 7+ years hands-on SAP experience (MM, PP, WM/EWM, SD, QM, APO, IBP, Ariba, etc.) Strong domain knowledge in Pharma, Manufacturing, or Supply Chain S/4HANA experience preferred Familiarity with GxP/GMP/FDA compliance is a plus

Easy Apply

Contract

Depends on Experience

Quality Technician 2

Sunnyvale, California

•

Today

Primary Function of Position Accessories Final Quality Inspection (AFQI) technician 2 will provide QA support by performing visual, dimensional and functional inspections of purchased assemblies and products. This position ensures acceptable quality standards ensuring incoming quality specifications have been met prior to release to finished goods. Essential Job Duties Perform incoming material inspections in a timely manner Perform First Article inspections on manuals Conduct visual, dimensi

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Contract

$32 - $32

Sourcing Manager

Hybrid in Foster City, California

•

2d ago

About Nexinfo; NexInfo is a consulting firm focused on improving business processes and automation in the Supply Chain and Product Lifecycle Management sectors. They offer services in business process design, software implementations, managed services, staff augmentation, and SaaS solutions. The company aims to help businesses across industries achieve their goals through industry best practices, lean process design, and advanced software solutions. Their ERP-related services address challenges

Easy Apply

Contract, Third Party

$70 - $80

Engineer/Scientist II, Quality Control

Los Angeles, California

•

Today

Work Schedule Environmental Conditions Job Description Thermo Fisher Scientific invites you to be part of our team and participate in impactful projects. Collaborate with dedicated colleagues and benefit from opportunities available within our respected organization. Location: West Hills, CA 100% onsite How will you make an impact: Using standard operating procedures (SOP) and good manufacturing practices (GMP), the Engineer/Scientist II will perform testing of Raw Material, Semi-finished,

Full-time

Scientist II

Pleasanton, California

•

Today

Software Guidance & Assistance, Inc., (SGA), is searching for a Scientist II for a contract assignment with one of our premier Pharmaceutical clients in Pleasanton, CA. Responsibilities : Will be a member of the Pharma Services/Research and Early Development Team in Pleasanton to support clinical sample processing which includes DNA extraction, library preparation, target enrichment and Next Generation Sequencing. Will also design, plan and execute assigned research and/or development-relat

Contract

USD 33.29 - 65.19 per hour

Metrology Engineer

Thousand Oaks, California

•

Today

Fully onsite at Thousand Oaks, CA Client maximum bill rate /hr** This summary provides a detailed overview of the Metrology Engineer position, outlining the key responsibilities, qualifications, and expertise required. The role emphasizes strong calibration skills, particularly in gas flow, and demands experience in pharmaceutical metrology within regulated environments. Position Overview The Metrology Engineer role requires a candidate with extensive gas flow calibration experience and the c

Full-time

Senior Assembly and Packaging Engineer

Santa Clara, California

•

Today

This Jobot Job is hosted by: Kurt Holzmuller Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $120,000 - $160,000 per year A bit about us: We are a diagnostics company dedicated to providing fast, affordable, and clinically relevant testing using advanced, automated laboratory technologies. Our accredited labs operate under stringent regulatory standards to deliver high-quality diagnostics to providers, hospitals, and patients nationwide. As

Full-time

USD 120,000.00 - 160,000.00 per year

Senior CSV Engineer

Remote or Massachusetts

•

Today

Job Description: We are looking for a Senior Computer System Validation (CSV) Engineer to perform validation of computerized systems associated with Client's facilities, utilities, and equipment for the qc lab validation project. This role will focus on EMS, Client, and laboratory informatics/software platforms (e.g., HPLC/qPCR control software, Sicknotes, Blue Mountain), ensuring compliance with 21 CFR Part 11, Annex 11, and data integrity requirements. The CSV Engineer will obtain documentatio

Full-time

2026 Future Talent Program - Global Workplace & Enterprise Services Maintenance & Engineering - Co-op

Remote or West Point, Pennsylvania

•

Today

Job Description Our Future Talent Program features co-operative assignments that last up to 6 months and will include one or more projects. These opportunities in our Global Services division can provide you with great development and a chance to see if we are the right company for your long-term goals. Job Description Our Support Functions deliver services and make recommendations about ways to enhance our workplace and the experience of working at our organization. The vision for the Global

Full-time

USD 39,600.00 per year

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GMP jobs in California, USA