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Cloud Data Engineer

CyberOne LLC

•

Chicago, Illinois, USA

Full-time, Third Party

We are seeking an experienced Cloud Data Engineer with a strong background in cloud platforms (AWS, Snowflake, Azure DevOps) and proficiency in Python and Spark. The ideal candidate will have 8 10 years of industry experience, preferably in the Life Sciences or Pharmaceutical domain, with hands-on expertise in cloud data integration and data migration projects. Knowledge of data warehousing concepts and best practices is highly desirable. Key Responsibilities:Design, develop, and maintain scalab
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Posted 12 days ago

Computer System Validation Engineer

Katalyst Healthcares and Lifesciences

•

Remote or New Jersey, USA

Full-time

Roles & Responsibilities: Full lifecycle validation for all applicable computerized systems, ensuring they are designed, validated, operated and retired in compliance with GxP regulation and computer system validation (CSV) guidance. Compiling and maintaining accurate CSV documentation, ensuring full traceability throughout system lifecycles. Compliance Analysis, Validation Planning, Risk Assessments Test planning and strategy creation and execution of test protocols, scripts and reports. V
Posted 60+ days ago | Updated 1 hour ago

CSV Engineer

Katalyst Healthcares and Lifesciences

•

Raritan, New Jersey, USA

Full-time

Role & Responsibilities: 3-7 years' experience in Computer System Validation or Quality management or Business Analysis in GxP application area. Has working experience in any one or two of the following domains Tool validation like ServiceNow, Automation tools, JIRA . Guide the project team with the right set of applicable project deliverables based on project type and category while catering to the SDLC. pplication of FDA guidance's and industry standards (i.e., GAMP). Strong understanding on 2
Posted 60+ days ago | Updated 1 hour ago

PMO Project Manager with a background in regulated environments

Combined Computer Resources

•

Ewing Township, New Jersey, USA

Contract

Role Summary The Project Manager is the single point of accountability for the delivery of one or more medium to large, complex business information technology projects involving multiple functions, delivering substantive value to business areas. This includes the structuring and detailed planning of the project work, management of the day-to-day work activities of the project, ensuring compliance to all applicable client processes, managing project scope, issues, risk, resources (internal and e
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Posted 7 hours ago

Infrastructure Business Analyst

TEKsystems c/o Allegis Group

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Branchburg, New Jersey, USA

Full-time

Description We are seeking a skilled and motivated Infrastructure Business Analyst to support IT initiatives within a regulated manufacturing environment in Branchburg, NJ. This role is ideal for professionals with a background in business analysis or project coordination, particularly within GMP-compliant pharmaceutical or manufacturing settings. You will play a key role in bridging the gap between IT infrastructure and operational technology (OT), ensuring seamless integration and compliance.
Posted 4 days ago | Updated 9 hours ago

Application Architect

TEKsystems c/o Allegis Group

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North Chicago, Illinois, USA

Full-time

MUST HAVE PROVEN ARCHITECT EXPERIENCE & EXPERIENCE WORKING WITHIN MEDICAL DEVICE/PHARMA/HEALTHCARE OR SIMILAR INDUSTRY Description We are seeking a highly skilled Application Architect to lead the technical design and architecture of a validated Complaints Management System upgrade for a Fortune 100 medical device company. This role is critical in ensuring the system meets enterprise standards, regulatory compliance, and business needs. The ideal candidate will bring deep expertise in enterprise
Posted 6 days ago | Updated 9 hours ago

Support Engineer

Veeva Systems

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Columbus, Ohio, USA

Full-time

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead. At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company - we made history in 2021 by becoming a public benefit corporation
Posted 47 days ago | Updated 12 days ago

Computer System Validation Engineer

Katalyst Healthcares and Lifesciences

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San Juan, San Juan, Puerto Rico

Full-time

Roles & Responsibilities: Full lifecycle validation for all applicable computerized systems, ensuring they are designed, validated, operated and retired in compliance with GxP regulation and computer system validation (CSV) guidance. Compiling and maintaining accurate CSV documentation, ensuring full traceability throughout system lifecycles. Compliance Analysis, Validation Planning, Risk Assessments. Test planning and strategy. creation and execution of test protocols, scripts and reports.
Posted 60+ days ago | Updated 1 hour ago

CAPA Quality Engineer (2 Openings)(ONSITE)(No C2C/H1B)

NetSource, Inc.

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Cedar Creek, Texas, USA

Contract

(No C2C/H1B) Please note that this is a 12 to 18-month contract position. Job Posting Qualifications Bachelor s or Master s Degree in biology, chemistry, biotechnology, engineering, or a related field, or equivalent experience.Post-graduate, Quality Assurance Certifications, such as Six Sigma, CQE, CQA, etc., is preferred.4+ years of experience in a similar position within the Life science/Pharma industry.Medical device regulations, such as ISO 13485, FDA 21 CFR part 820, and IVDR 2017/746 is re
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Posted 2 days ago | Updated 2 days ago

Process Engineering

Johnson & Johnson

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Jacksonville, Florida, USA

Full-time

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
Posted 9 days ago | Updated 1 hour ago

Lead UX designer

Motion Recruitment Partners, LLC

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Boston, Massachusetts, USA

Full-time

A fast-growing scientific data company is hiring a Senior UX Designer to lead the development of AI-powered enterprise design systems. This role is a remote, contract-to-hire opportunity focused on building scientific AI workflows for regulated industries like life sciences and healthcare. You'll be designing mission-critical interfaces that bridge scientific research with machine learning applications including assays, lab instrumentation, and model output visualizations. This is a consulting g
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Posted 7 days ago | Updated 9 hours ago

Tosca Test Architect

HPTech Inc.

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San Francisco, California, USA

Third Party, Contract

Job Title: Tosca Test Architect SAP S/4HANA Test Automation Location: Bay Area (Mandatory to be in office every week) Experience: 10+ years in QA with 3+ years as Test Architect Industry: Life Sciences Job Summary: We are seeking a seasoned Tosca Test Architect to lead the automation strategy and test architecture for SAP S/4HANA implementations, specifically focusing on Plan-to-Make and Order-to-Cash business processes. The ideal candidate will bring deep expertise in Tosca, SAP testing framew
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Posted 6 days ago | Updated 6 days ago

Learning Management System (LMS) Administrator Specialist

Sunrise Systems, Inc.

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Lawrence Township, New Jersey, USA

Contract

Job Title: Learning Management System (LMS) Administrator Specialist Job ID: 25-08974 Location: Lawrence Township, NJ Duration: 05 months on W2 Contract Must Have List: B.S in education, science, or related discipline or equivalent experience.Minimum of 3+ years experience of ELMS, preferably SuccessFactorsMinimum of 3+ years experience in a training / learning organization / function3+ years of MS Office This position is responsible for the accurate and timely processing of all training re
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Posted 29 days ago | Updated 8 hours ago

Lead Engineer - MES Opcenter

Katalyst Healthcares and Lifesciences

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Remote or New York, USA

Full-time

Job Description: The Lead Engineer will lead a team of technical resources to design, develop, configure, and test MES (Manufacturing Execution Systems) solutions. They will be directly responsible for leading resources contracted vi third-party and through other Pharmaceutical organizations to develop & deploy MES application software to Medical Device manufacturing sites globally. Responsibilities: Act as subject matter expert on system design and architecture. Solutioning and designing new
Posted 29 days ago | Updated 1 hour ago

CSV Engineer

Katalyst Healthcares and Lifesciences

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Massachusetts, USA

Full-time

Job Overview: Our client seeking an experienced CSV / IT GxP Consultant. This role will focus on ensuring the alignment of internal policies with federal and state regulations, improving our Computer System Validation (CSV) processes, and enhancing third-party vendor compliance. The position will also involve developing and implementing SOPs, as well as managing data privacy and retention policies. The ideal candidate will have experience in GxP regulations and a strong understanding of IT proce
Posted 60+ days ago | Updated 1 hour ago

Validation Support Engineer

Katalyst Healthcares and Lifesciences

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Johns Creek, Georgia, USA

Full-time

Roles & Responsibilities: Validation Planning: Develop/update Master Validation Plans (MVP) and individual Validation Plans (VP) for system changes. Required: Proven expertise in CSV (Computer System Validation) methodologies (e.g., GAMP5), FDA regulations (21 CFR Part 11, 210, 211, 820 as applicable), and validation of automated manufacturing/control systems. Experience validating PLC-based systems (Beckhoff Twin CAT experience is a significant plus). Responsibilities: Perform tasks under S
Posted 60+ days ago | Updated 1 hour ago

CSV Engineer (Computer System Validation)

Katalyst Healthcares and Lifesciences

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Kansas City, Missouri, USA

Full-time

Roles & Responsibilities: Validation documentation Authoring (validation plans, user requirements specifications, risk assessment, IQ-OQ-PQ protocols, trace matrix and summary reports). Experience in validating GMP Lab systems and Equipment. Responsible for assuring a system/application meets its requirements as outlined in system specification (URS/FRS) per process defined in the Validation Plan for the project. Identify and escalate, as necessary project risks and issues to the CSVC Manage
Posted 60+ days ago | Updated 1 hour ago

SAP Integration Lead

Judge Group, Inc.

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Boston, Massachusetts, USA

Contract

Location: Boston, MA Salary: $75.00 USD Hourly - $80.00 USD Hourly Description: Job Title: SAP Integration Lead Location: Boston, MA (Hybrid) Duration: 6+ months Contract Need Locals Only Required Qualifications: Bachelor's degree in Computer Science, Engineering, Life Sciences, or a related field8+ years of SAP integration experience, with 3+ years in a regulated pharmaceutical environmentExpertise in SAP CPI, PI/PO, IDoc/ALE, RFC, BAPI, and API-based integrationStrong understanding of SAP
Posted 29 days ago | Updated 10 hours ago

QA Lead Technical Operations

TSR Consulting Services, Inc.

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Harvard, Massachusetts, USA

Contract

Our client, a leading pharmaceutical company, is hiring a QA Lead - Technical Operations, on a contract basis. Job ID: 82974 Work Location: Devens, MA - on site Education/Experience: Knowledge of science generally attained through studies resulting in a B.S; in Biological science, Engineering biochemistry, or related discipline, or its equivalent is preferred. Advanced Level of relevant experience in a GMP, Google Cloud Platform, or GXP with at least 8 years focused on product quality. Preferred
Posted 22 hours ago | Updated 10 hours ago

QA Lead Technical Operations

LOGIXtech Solutions

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Harvard, Massachusetts, USA

Contract

Our client, a leading pharmaceutical company, is hiring a QA Lead - Technical Operations, on a contract basis. Job ID: 82974 Work Location: Devens, MA - on site Education/Experience: Knowledge of science generally attained through studies resulting in a B.S; in Biological science, Engineering biochemistry, or related discipline, or its equivalent is preferred. Advanced Level of relevant experience in a GMP, Google Cloud Platform, or GXP with at least 8 years focused on product quality. Preferred
Posted 22 hours ago | Updated 10 hours ago