Document Management Specialist, GXP - Princeton

The GxP Document Management Coordinator will perform delegated tasks related to GxP procedural and governance document management. · ...

+Job summary · The Laboratory CART Run Support Lead will provide laboratory computing and scientific application support to all scientists associated with the client CART manufacturing pods and QC Labs This is an onsite role in Raritan NJ. · +ResponsibilitiesManage requestsincide ...

Pay Rate Low: 50 | Pay Rate High: 60 · A growing, well-funded biotech company is seeking a Veeva Quality Systems Specialist to provide hands-on operational support within a Veeva Basics Quality Vault environment. This is an execution-focused role supporting daily Quality Systems ...

We are seeking an experienced Lead Validation Specialist with experience in clinical systems to join our team. · ...

Pay Rate Low: 50 | Pay Rate High: 60 · A growing, well-funded biotech company is seeking a · Veeva Quality Systems Specialist · to provide hands-on operational support within a Veeva Basics Quality Vault environment. This is an execution-focused role supporting daily Quality Syst ...

We are seeking an experienced Lead Validation Specialist with experience in clinical systems to join our team. · This is an ideal opportunity for someone who thrives in fast-paced, dynamic environments where adaptability, critical thinking and initiative are essential.About the R ...

Join our client as a Document Management Specialist II. · ...

Join our client as a Document Management Specialist II, where you'll play a key role in enhancing document management processes. Collaborate with various teams to ensure the smooth operation of document management initiatives and support continuous improvement efforts. · ...

Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four disease areas: bone and mineral; intractable hematologic; hematology oncology; and rare disease. A Japan-based compa ...

We are seeking a Security Operations & OT Cybersecurity Specialist to join our Global Information Security team.This role will serve as the regional lead for North America security operations and OT/ICS security, responsible for incident response, monitoring, and cyber defense ac ...

We are seeking a dynamic and experienced Head of Cybersecurity, North America & Global SOC Leader to join our Global Information Security Team This role will serve as the senior security leader for the North America region while also leading our global Security Operations Center ...

· Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four disease areas: bone and mineral; intractable hematologic; hematology oncology; and rare disease.  A Japan-based c ...

We are hiring Application Testing Specialists for one of our clients. · Working with the Hosting Services and Cloud Hosting Services teams (Client and Full-Stack Enterprise Service Providers) to assess new and existing infrastructure components/resources installations (server, DB ...

Working with Us · Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production lin ...

We are seeking a skilled Technical Writer/Procedure Document Specialist to collaborate with colleagues, customers and stakeholders on projects focused on process enhancement and continuous improvement within the CMR Strategic Operations,GxP Compliance & Technical Operations. · De ...

Job Summary · We are seeking a skilled Technical Writer/Procedure Document Specialist to collaborate with colleagues, customers, and stakeholders on projects focused on process enhancement and continuous improvement within the CMR Strategic Operations, GxP Compliance & Technical ...

We are seeking a skilled Technical Writer/Procedure Document Specialist to collaborate with colleagues, customers, and stakeholders on projects focused on process enhancement and continuous improvement within the CMR Strategic Operations, GxP Compliance & Technical Operations. · ...

We are seeking a skilled Technical Writer/Procedure Document Specialist to join our team for a 12-month contract opportunity. This role will focus on developing procedural documentation within a GxP environment, ensuring compliance, operational effectiveness, and supporting proce ...

Job Summary · We are seeking a skilled Technical Writer/Procedure Document Specialist to collaborate with colleagues, customers, and stakeholders on projects focused on process enhancement and continuous improvement within the CMR Strategic Operations, GxP Compliance & Technical ...

We are seeking a skilled Technical Writer/Procedure Document Specialist to collaborate with colleagues, customers and stakeholders on projects focused on process enhancement and continuous improvement within the CMR Strategic Operations. · ...