Veeva jobs

No location provided

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Today

Position: Veeva System Developer Duration: 6 months Location: Remote Description Collaborate on the design and lead the implementation of Enterprise Applications solutions tailored to specific business applications or technologies, aligning with enterprise business strategy and requirements. Administer, configure, and optimize Veeva Vault PromoMats to support the Quality Management System (QMS). Develop custom solutions and integrations to automate workflows, enhance system capabilities, and en

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Full-time, Contract

Data Management Transformation Leader

Remote or Hybrid in Thousand Oaks, California

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Today

Client: global biotech company Job: Data Management Transformation Leader Job type: 1 year contract, open to extensions Location: 100% remote from the US Pay: open market rate Job Description:Purpose: To provide expertise in data management processes, demonstrating capabilities & new ways of working, to assist in the design and implementation of both new technologies, new processes.Clinical Trial Delivery Operating Model: Develop Data Management playbook to encompass new ways of working with key

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Contract

BASED ON EXPERIENCE

Clinical Data manager

Remote

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30+d ago

Need stronger with working on Data Acquisition, DTAs and vendor relations. Responsibilities: Support the planning, setup, and acquisition of external clinical data at the study level, assisting in managing study start-up, conduct, and closeout activities.Assist in creating external data transfer agreements, ensuring alignment with Takeda Standards and specifications to support data integration, analysis, and reporting.Provide support in setting up infrastructure for external data to flow into T

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Contract, Third Party

Depends on Experience

CQV Engineer

Pittsburgh, Pennsylvania

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Today

Job Description: Our client is currently building (started in 2024) a 125,000 sq ft greenfield manufacturing facility outside of Pittsburgh, PA. Expected to be operational by 2027 Q1. The electricity gets turned on in this facility in the end of Jan 2026. The facility will be state of the art and will be in partnership with U of Pitt. It will be focused on Gene Editing, iPSC tech, and cell, vector and protein engineering capabilities. Our client is looking to add an Owner's Rep CQV Engineer to h

Full-time

CSV Engineer

Franklin Township, New Jersey

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Today

Roles & Responsibilities: We are now looking for a resource on the validation side of things going on here. Depending on the resource, we're looking for someone with (LabVantage) LIMS and quality systems validation experience, and/or general more broad Pharma/Biotech CSV experience that could back-fill as staff augmentation. Engagement would be (at least) through the end of the year. Potential in-scope activities. i. CSV/Lab Systems Qualification document/deliverable authoring. ii. Test scr

Full-time

Senior Clinical Data Manager

Remote

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Yesterday

100% Remote Job Description Senior Clinical Data Manager Role Overview We are seeking an experienced Clinical Data Manager (CDM) to support multiple outsourced clinical studies. The ideal candidate will have strong hands-on expertise in EDC systems, data review activities, vendor data reconciliation, and CRO oversight. Responsibilities Manage 4 concurrent clinical studies outsourced to CROs, ensuring data integrity and compliance. Oversee day-to-day data review activities in the EDC, including

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Contract, Third Party

$50 - $90

Regulatory CMS Senior Manager

Remote

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29d ago

C2C Role Please share Profiles at Hi, Urgent need, Job Title: Regulatory Studio CMS Senior Manager Work location: New Brunswick (preferred), Lawrenceville Monday thru Friday - Normal business hours, with some flexibility 50% onsite - Team is onsite Monday thru Thursday Top 3 to 5 skills/Must Haves: Small Molecule Drug development experience (2 to 3 years) Good communications skills (written/verbal) Experience with Veeva System PREREQUISITES BS/BA degree in Scientific Discipline (master's or hig

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Contract, Third Party

$50 - $60

Remote Consulting Project Manager - SAP Supply Chain Management (Pharmaceutical Industry)

Remote

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Today

Our client is seeking a remote Consulting Project Manager, initially on a fractional basis (~15-20 hours weekly), with SAP Supply Chain Management experience within the Pharmaceutical industry. The initial length of assignment will be 6 months to start, with potential for one or multiple extensions. The Consulting Project Manager will be responsible for, but not limited to, the following: Act as the Project Manager for the SAP SCM implementation from inception to go live and post production su

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Contract

Depends on Experience

Senior Integrated Market Specialist

No location provided

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2d ago

Join our dynamic team as a Senior Integrated Marketing Communications Specialist where you will shape the brand presence and drive impactful results through innovative marketing campaigns. Collaborate with cross-functional teams to create and execute high-quality promotional programs that align with business objectives and enhance our brand. Responsibilities Develop and implement comprehensive integrated marketing plans in collaboration with cross-functional teams. Lead the creation of engaging

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Contract

Depends on Experience

GMP Tester / Validation Engineer

Vacaville, California

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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

Full-time

Senior Validation Engineer

Lexington, Massachusetts

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Today

Responsibilities: Shire Human Genetic Therapies Inc. is seeking a Senior Validation Engineer with the following duties: Write Validation documents per Food Drug Administration (FDA)/Company guidelines; draft Specification documents and Validation Plans (VPs) for pharmaceutical manufacturing and laboratory equipment; Write and execute qualification protocols for new equipment and decommissioning protocols for old equipment. Execute approved protocols per company Good Documentation Practices (cG

Full-time

Data Steward - III (Advanced)

Rahway, New Jersey

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15d ago

Job Title: Data Steward - (Advanced) Job ID: 25-09671 Location: Rahway, NJ Duration: 04 months on W2 contract Qualifications: Education: BS/BA Information Systems, Information Technology, Computer Science, Human Computer Interaction or related disciplines Required Experience and Skills: Need a Strong technical backgroundProven experience as a developer in PowerApps, specifically around integrating API calls/endpoints to retrieve live data in real time.Proven experience with Microsoft Platform

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Contract

$62 - $68.25

Senior Validation Engineer

Lexington, Massachusetts

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Today

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description Pursuant to Section 20 C.F.R. 656.10, you are hereby notified that an application for Alien Employment Certification will be filed by

Full-time

USD 132,000.00 - 193,300.00 per year

IT Business Relationship Manager - (North America Sales Operations)

Alameda, California

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Today

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. Yo

Full-time

USD 112,000.00 - 224,000.00 per year

Computer System Validation Engineer

Bothell, Washington

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Today

Job Description: The Computer Systems Validation (CSV) Contractor works cross-functionally to lead and execute validation activities for GxP electronic systems and applications. This role is an individual contributor. The CSV Contractor will partner with Business Owners, Technical Owners, and Quality to create and manage validation deliverables for electronic systems and applications throughout the validation lifecycle. The CSV Contractor has primary responsibility to ensure that the tasks suppo

Full-time

Quality Systems Specialist II - Data Integrity (388)

Petersburg, Virginia

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Today

About Civica: Critical shortages of essential generic injectable drugs are an ongoing crisis in U.S. healthcare and have reached an all-time high. Over 300 essential medications are currently reported to be in shortage, according to industry and FDA reports. Shortages put patients at risk and waste hospital resources. Civica is a market-based nonprofit solution created in 2018 by health systems and philanthropies for the express purpose of preventing and mitigating drug shortages. Today, near

Full-time

Principal Associate - Global HSE Systems and Data Manager

Indianapolis, Indiana

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Today

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined

Full-time

USD 63,000.00 per year

Lifesciences CRM Architect

No location provided

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Today

Job Summary: We are seeking an experienced Life Sciences CRM Architect to design, implement, and optimize CRM solutions that support commercial, medical, and patient engagement strategies within the life sciences industry. You will be responsible for defining CRM architectures, integrating systems, and aligning business objectives with CRM platforms (e.g., Salesforce, Veeva, Dynamics 365). Your expertise will help drive better customer engagement, data management, and regulatory compliance acro

Third Party, Contract

Specialist IS Bus System Analyst

Remote or New Albany, Ohio

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Today

Career Category Information Systems Job Description Join Amgen's Mission of Serving Patients At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of pati

Full-time

USD 115,058.00 - 143,472.00 per year

Software Quality Engineer

Secaucus, New Jersey

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Today

Job Description The Software Quality Engineer (SQE) within Quality and Regulatory organization plays a critical role in ensuring that software whether embedded in products, supporting clinical workflows, or used in enterprise quality systems meets rigorous internal quality standards and global regulatory requirements. The SQE is responsible for driving and executing software validation activities across the development lifecycle, contributing to design control, risk management, and audit readi

Full-time

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