GxP jobs in Chesterbrook, PA

Collegeville, Pennsylvania

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7d ago

Job Title:Lab Desktop Engineer with GxP Location:Collegeville, PA - 100% ONSITE FROM DAY 1 Duration: 6+ Months Contract Make sure candidate should have pharmaceuticals or life sciences domain Key responsibilities: Assist in maintaining existing computer infrastructure of 5000 PCs globally.Image/Onboard new computers into the domain and onto the network and decommission it.Secure and protect new and existing hardware.Consult with the business as they require assistance with their equipment.Troubl

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Contract

Depends on Experience

IT Project Manager with GxP

Remote

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3d ago

Title: IT Project Manager with GxP Location: Boston MA (1x Month) Duration: 6 Months Visa: No H1b Need an IT/Infrastructure PM with recent Pharma and GXP experience. Must have experience working with MSPs or Vendors Description: The Project Manager will be responsible for the end-to-end project lifecycle of multiple simultaneous IT projects in a GxP regulated environment. The PM will engage in new and in-flight projects to ensure project resources are aligned to deliver on schedule and within

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Full-time

70 - 75

Project Manager - Pinnacle 21, GXP | 100% Remote | Contract

Remote

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4d ago

Our direct client a large global R&D driven pharmaceuticals company is seeking to hire a Project Manager for their Pinnacle 21 upgrade project.This is 6 months plus contract. Job Title: Project Manager - Pinnacle 21 upgrade project Duration: 6 months (may extend) Location: 100% Remote (work per eastern time)Pinnacle 21 solution is critical for SQS.For this role client is looking for System upgrade experience as a Project Manager and from IT perspective.The tool provides the quality of submissio

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Contract

Depends on Experience

Google Cloud Platform Data Architect

Collegeville, Pennsylvania

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Today

Hi Vendors, Need Google Cloud Platform Data Architect Google Cloud Platform Data Architect Knowledge of development and maintenance of Canonical Data Models (CDM) and domain-specific data models Knowledge of GenAI, LLM, Agentic AI Definition and governance of scientific ontologies and controlled vocabularies Design and implementation of data governance frameworks covering classification, data quality, lineage, retention and GxP / regulatory compliance. " Design of enterprise data architectu

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Full-time, Part-time, Third Party, Contract

Vaccines Safety Sciences Lead

King of Prussia, Pennsylvania

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Today

Responsibilities: ? Manages and directs functions to comply with standard operating procedures, regulatory safety and pharmacovigilance and business technology quality standards in compliance with national and international regulations, such as relevant GxP guidelines and national and international legislations and regulations as well as aggregate safety reports in area of responsibility. ? Oversees evolving pharmacovigilance legislations and provides strategic direction for implementation of re

Full-time

Computer System validation Engineer

Wilmington, Delaware

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Today

Hi, Title:Computer System validation Engineer Compute System Validation(CSV) with R&D Knowledge Qualification: Bachelor of Science OR Bachelor of Technology OR Bachelor's in Pharmacy Experience: Over 8+ years of overall experience with at least 5 years of experience in Computer System validation for GxP system Knowledge, Experience and Skills: { CORE CSV 21 CFR Part 11/820, GxP, GAMP 5, SOX, EU Annex 11/22, ISO 9001, ITIL, EU Anness 22, ISO 9001, ITIL, Audit/inspection readiness, periodic r

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Full-time, Part-time, Third Party, Contract

lab Engineer

Collegeville, Pennsylvania

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Today

Hi, lab Engineer. Job Description (JD) Lab Engineer (R&D Laboratory Technology Support) Position Summary We are seeking a highly motivated Lab Engineer to support and maintain laboratory computing environments, scientific instrumentation, and technology infrastructure within a global Research & Development (R&D) organization. The successful candidate will partner closely with scientists, researchers, and business stakeholders to ensure laboratory systems remain secure, reliable, compliant, and o

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Full-time, Part-time, Contract, Third Party

Computer System Validation Engineer

Wilmington, Delaware

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Today

Roles & Responsibilities : 21 CFR Part 11/820, GxP, GAMP 5, SOX, EU Annex 11/22, ISO 9001, ITIL, EU Anness 22, ISO 9001, ITIL, Audit/inspection readiness, periodic reviews, access roster and audit trail reviews, Deviation/CAPA management, SOP/policy compliance processes uthoring of URS/FS, protocols, final reports, validation plan/report High-level understanding of Veeva Vault suits Risk-based testing aligned to CSA fundamentals High-level understanding of Biostatistics, Clinical, Discovery, Med

Full-time

Senior Automation Engineer

Malvern, Pennsylvania

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Today

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn m

Full-time

USD 79,000.00 - 120,700.00 per year

Senior Validation Engineer

King of Prussia, Pennsylvania

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Today

Business Introduction: We manufacture and supply reliable, high-quality medicines and vaccines to meet patients' needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it's vital to bringing our innovations to patients as quickly, efficiently and effectively a

Full-time

Sr. Specialist, Engineering

West Point, Pennsylvania

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Today

Job Description The Senior Specialist of Automation serves as the BAS/HVAC technical authority for West Point, GWES Southeast Pennsylvania. The senior specialist is responsible for automation system performance, compliance, reliability, energy optimization, and lifecycle management. The position provides technical leadership to specialists and technicians while leading capital projects, managing change controls, supporting audits, and maintaining BAS systems in a state of GMP compliance. Key R

Full-time

USD 117,000.00 - 184,200.00 per year

Lead Solution Architect

Remote

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10d ago

Lead Solution Architect Remote (Eastern Time Zone) Location: Remote (must be available to work in the Eastern Time Zone)Travel: Up to 25% travel to client site in North Carolina as needed. About the RoleWe are seeking a highly skilled Enterprise Architect for a Greenfield manufacturing facility project, who will be the site team liaison between IT and business cross functional teams to ensure the quality delivery of 40+ digital capabilities for the new site from an architecture perspective.Key R

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Contract

Depends on Experience

OT Systems Engineer

King of Prussia, Pennsylvania

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Today

Provide direct engineering and technical support of site operating technology (OT) networks and systems. Evaluate and develop technology, plan and implement modifications, maximize network/system security and performance, and ensure operability of various controls, digital, and execution systems, and their integrations. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following: Provide maintenance and lifecyc

Full-time

Agilent OpenLAB CDS Analyst

Remote

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Today

Job title: Agilent OpenLAB CDS Analyst Work Location: Rahway, NJ (Remote with Travel) Duration: Long Term Contract Job Description The Senior Technical Analyst will be responsible for supporting configuration, build, validation, & release activities for the successful release of a global enterprise Agilent OpenLAB CDS 2.x platform (OL:CDS), supporting and managing lab deployment resources in Agilent Instrument Controllers (AIC) builds, deployments, & troubleshooting efforts, and oversight of po

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Contract

Depends on Experience

Product Manager - Veeva Vault

Remote

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10d ago

Role: Veeva Vault Product Manager Location: Remote Job Type: FTE/ Full- Time Experience Range: 10- max 22 years Primary Skills: 1. Experience with system integrations (e.g., CTMS eTMF/EDC/Data Lakes & repositories) 2. Experience working with Siebel (CTMS) 3. Experience working with Veeva Managed Services or vendor escalations 4. Familiarity with Agile or DevOps methodologies 5. Knowledge of clinical metrics and reporting tools Required Bachelors degree in Life Sciences, Information Systems, o

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Full-time

Depends on Experience

Senior Specialist, Master Data Quality Management, Hybrid

West Point, Pennsylvania

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Today

Job Description As part of the Global Clinical Supplies (GCS) Organization, the Sr. Specialist, Master Data Quality Management is responsible for driving data quality, governance, stewardship, and operational excellence across critical master data domains supporting Global Clinical Supply Operations (GCSO). This role helps ensure that master data is accurate, complete, compliant, and fit-for-purpose to support planning, manufacturing, packaging, distribution, regulatory compliance, and business

Full-time

USD 117,000.00 - 184,200.00 per year

Veeva Vault Product Manager

Remote

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6d ago

Veeva Vault Product Manager Clinical SME | Remote | FTE Location: Remote Employment: FTE Experience: 1022 Years We are hiring an experienced Veeva Vault Product Manager / Clinical Systems SME with strong expertise in Veeva Vault Clinical (CTMS & eTMF) and clinical trial operations. Key Requirements: 812+ years of experience delivering/leading regulated enterprise or clinical systems initiatives Deep hands-on experience with Veeva Vault Clinical CTMS & eTMF Strong understanding of clinical tria

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Full-time

Depends on Experience

Senior Director, Light-Track Delivery & AI Automation

Remote

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Today

About Parexel Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere. We work with focus, agility, and shared purpose -- moving with urgency to address patient needs and accelerate

Full-time

Senior Technical Business Analyst

Remote

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6d ago

DescriptionJob Title: Senior Healthcare Business Analyst Type: Part Time Experience Level: Senior Seeking a highly skilled and experienced Senior Business Analyst responsible for bridging the gap between business objectives and technology solutions, ensuring that our projects align with organizational goals and deliver maximum value. You will utilize your expertise in business analysis and data-driven decision-making to identify opportunities for improvement and drive successful project outcomes

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Part-time

Depends on Experience

Associate Director - Process Engineering

Pennsylvania

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Today

Business Introduction At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people's lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating sign

Full-time

GxP jobs in Chesterbrook, PA, USA