GxP jobs in New Jersey

Business Analyst – Pharma/GxP/Data Governance/Gen AI

Remote

•

Today

Business Analyst Pharma/GxP/Data Governance/Gen AILocation: RemoteExperience: 8+ YearsDomain: Pharma / Life Sciences Job DescriptionWe are seeking an experienced Business Analyst with strong Pharma/Life Sciences domain expertise to support initiatives focused on Data Quality, Regulatory Compliance, and Generative AI (Gen AI) within GxP-regulated environments. The ideal candidate will work closely with Quality, Regulatory, Data Science, and Technology teams to drive compliant digital transformat

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Contract

Depends on Experience

TrackWise

Remote

•

Today

TrackWise - Remote Experience wth TrackWise 9/10.x versions Strong knowledge on Oracle PL/SQL Strong knowledge on Crystal Reports Excellent communication skills both for client and interpersonal Experience with ITIL and SDLC Methodologies Experience on Migration Good experience of managing CAPA, Deviation and PR (Periodic Review) Good-to-Have Good Knowledge on configuration Prior experience of working on support and maintenance environment Undertanding of Good Documentation Practice (

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Contract, Third Party

Depends on Experience

TrackWise Support Engineer - W2 Position

Remote

•

Today

Hi, The following requirement is open with our client. Title : TrackWise Support Engineer Location : Remote Duration : 12+ Months Rate :$55/hr on W2 Position : W2 Position Relevant Experience (in Yrs.): Job Description: (Ideally should not be more than 3-5) Experience wth TrackWise 9/10.x versions Strong knowledge on Oracle PL/SQL Strong knowledge on Crystal Reports Excellent communication skills both for client and interpersonal Experience with ITIL and SDLC Methodologies Experience

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Full-time

54 - 55

Data Engineer

Bridgewater, New Jersey

•

7d ago

We are seeking a Senior Data Engineer to build and operate enterprise-grade data pipelines using Microsoft Azure as the orchestration layer and Snowflake as the enterprise data lake/warehouse. This role focuses on reliable ETL/ELT, push/pull data integration patterns, and scalable platformengineering in a GxP / validated environment. Key Responsibilities Design and build batch and incremental data pipelines using Azure-native orchestration services to move data into and out of Snowflake.Support

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Contract

65 - 75

Sr SDET

Remote

•

Today

Role: Sr. SDET (IOT and Cloud testing background) Must have: Handson experience testing (Manual and Automated) of IoT / Edge / devicebased systems, including Linux and Ubuntu environmentsCloud testing experience (Azure preferred)Strong proficiency in Python, API testingGood communication Preferred: Experience with Life science programs - Medical Devices, Digital Surgery Platforms, or IoMTExperience working in GxP regulated environments

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Full-time

Depends on Experience

Sr. Computerized System Validation (CSV) Manager

Remote

•

Today

We are Looking for a Senior Computerized System Validation (CSV) Manager with CRO industry experience. This a full-time permanent hire position with our client. In this role you can work fully remote (anywhere in USA). In this role as a Senior Computerized System Validation (CSV) Manager, you will lead the transformation of CSV practices within the organization. In this role as a Senior Computerized System Validation (CSV) Manager you will ensure validation processes are risk-based, efficient, a

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Full-time

Depends on Experience

Principal Cloud Infrastructure Engineer

Remote

•

Today

Job Title: Principal Cloud Infrastructure Engineer (Google Cloud Platform & DevOps, Life Sciences) Duration: 6+ Months Location:United States Remote / Some Boston and/or San Diego travel may be required during the engagement Overview At our Biotech client, data is its most valuable asset. We are hiring a Principal Cloud Infrastructure Engineerto advise on the evolution of the Google Cloud Platform (Google Cloud Platform) ecosystem. You will be the architect and executor (hands on)of a secure, s

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Part-time

Depends on Experience

CSV-Validation/(Good Clinical Practice)

Hybrid in Independence Township, New Jersey

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2d ago

This position involves validation strategy and planning, executing, and qualification of computer systems and/or infrastructure components in accordance with applicable policies, procedures, and regulatory requirements. Responsibilities:Define validation strategy for computerized systems and platforms utilized in GxP SpaceCreate validation deliverables such as Validation Plan, Test Protocols, Traceability matrix, and execution of protocolsParticipate in user review meetings, discussions with Qua

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Full-time

Depends on Experience

SAP PP/PP-PI Consultant S/4HANA Program (Pharma/Life Sciences)

Remote

•

Today

Role Overview: We are seeking a seasoned SAP PP/PP-PI Consultant to join our S/4HANA program, supporting complex production planning in a regulated (GxP) environment. This role requires deep expertise in pharmaceutical/life sciences manufacturing processes and advanced SAP PP-PI capabilities. Key Responsibilities: Manage production planning for radioactive materials, including half-life considerations, scrap handling, and scheduling.Simplify and optimize PI Sheets and process order execution.En

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Contract

Depends on Experience

Regulatory Affairs Project Manager

Remote or Jersey City, New Jersey

•

Today

Job Title: Regulatory Affairs Project Manager - Small Molecule (20 Hrs/Week) Location: Remote Job Description We are seeking an experienced Regulatory Affairs Project Manager with strong expertise in Small Molecule pharmaceutical products. The ideal candidate will lead regulatory submission activities, coordinate cross-functional teams, and ensure compliance with global regulatory requirements. Required Skills & Qualifications Bachelor s or Master s degree in Pharmacy, Life Sciences, Chemistry

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Contract

EDI / Middleware integration lead

Remote or California

•

Today

Job Title : EDI / Middleware integration lead Location : Remote. Key Responsibilities Design and lead EDI/Middleware integration solutions across SAP ECC/S4HANA Handle B2B integrations (EDI, MFT) using IBM B2Bi / Axway Support S/4HANA migration and large-scale interface transformations Build and optimize data mappings, APIs, and integration frameworks Drive automation and AI initiatives (Copilot, Power Automate) Ensure delivery in regulated environments (Pharma/GxP) Required Skills EDI: ANSI X12

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Third Party, Contract

$DOE

Nextflow Engineer

Remote or New York, New York

•

Today

RESPONSIBILITIES: Kforce has a client that is seeking a Nextflow Engineer in New York, NY. Summary: We are seeking a strong Nextflow Pipeline Engineer to support a new client engagement focused on genomic sequencing and bioinformatics workflows. This is an initial project engagement as part of a growing relationship, with the opportunity to contribute to foundational data engineering efforts in a highly specialized domain. Key Responsibilities: * Lead and support data engineering engagements

Contract

$60 - $70 hourly

Engineer III

Branchburg, New Jersey

•

Today

Location: Branchburg, NJ (Hybrid) Responsibilities: Serve on project technical team, consisting of cross-functional resources including but not limited to R&D, PDS&T, Quality, Biocompatibility, and Regulatory. Partner with R&D to identify user and technical product requirements for a medical device product. With Technical Lead, develop Design Verification & Validation strategy. Support Design Verification (planning, fixture development, method development, test method validation, protocol devel

Full-time

CSV Engineer

New Jersey

•

Today

Summary: IT CSV Validation Engineer is responsible for authoring and executing validation test scripts to support regulated systems within a GxP life sciences environment. This role will focus on validating ERP Master Data Governance processes and Data Lake platforms, ensuring compliance with regulatory requirements and data integrity standards. Roles & Responsibilities: Author, review, and execute validation test scripts (IQ/OQ/PQ) for GxP computerized systems Support validation activities fo

Full-time

Business Analyst

Remote

•

Today

Business Analyst (w2 only)Introduction:This position sits at the intersection of Data Quality, Regulatory Compliance, and Generative AI (Gen AI), driving digital transformation in GxP-regulated environments. The Business Analyst will collaborate closely with Quality, Data Science, and Technology teams to enhance AI-enabled quality processes, ensure data integrity, and foster compliant innovation. Responsibilities:Partner with Quality, Regulatory, and Business stakeholders to gather and formalize

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Full-time

Depends on Experience

Bioinformatics Pipeline Validation Manager with Cancer genomics exp (Remote -US)

Remote

•

22d ago

Bioinformatics Pipeline Validation Manager with Cancer genomics exp (Remote-US) We are looking to hire a candidate with the skills sets mentioned and experience for one of our clients within the life science Industry. Location:Flexible (Remote) Must overlapat least 5 hours with ESTdaily Job summary We are seeking an experienced Bioinformatics Pipeline Validation Manager with Cancer genomics and Clinical diagnosis experience to lead validation efforts for bioinformatics pipelines. This individ

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Contract

Depends on Experience

AI Leads - Clinical/Drug Substance/Drug Product with CDMO (Contract Development and Manufacturing Organization) Exp. (Remote)

Remote

•

28d ago

AI Leads - Clinical/Drug Substance/Drug Product with CDMO (Contract Development and Manufacturing Organization) Exp. (Remote) We are currently looking for three AI Leads to drive AI innovation across key areas of a Life Sciences/Biopharma organization: AI Lead Clinical Trial (CT)AI Lead Drug Substance (DS)AI Lead Drug Product (DP) These roles will act as forward deployed AI Leaders, responsible for identifying high impact opportunities and delivering scalable AI/GenAI solutions that improve bus

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Contract

Depends on Experience

Validation Engineer

Fairfield, New Jersey

•

Today

Validation Engineer Needed For Leading Medical Device Manufacturer This Jobot Job is hosted by: Kevin Finlay Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $100,000 - $110,000 per year A bit about us: My client is a leading medical device manufacturing company and is growing! They are looking to add a Validation Engineer who will be responsible for Validation/PPAP Packages on new customer programs, as well as ensuring compliance is applica

Full-time

USD 100,000.00 - 110,000.00 per year

Director IT Business Enablement - Manufacturing & Quality - USA Remote

Remote

•

Today

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed

Full-time

USD 190,000.00 - 215,000.00 per year

Senior Veeva Business Analyst - PV W2

Remote

•

Yesterday

Job Description - Title :- Senior Veeva Business Analyst Remote Duration :- 12+ Months MOI :- Skype Linkedin :- Must 20 years experience Pharma or life Science Domain -Must Primary Skills(must-haves): Bachelor s degree in Life Sciences, Information Systems, or related field Deep hands-on experience Veeva Vault Clinical (CTMS + eTMF), Siebel CTMS, Integration & Migration hands on 8 12+ years of experience delivering or leading regulated enterprise or clinical systems initiatives Strong unders

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Contract

$50 - $70

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GxP jobs in New Jersey, USA