Validation Test lead with Trackwise - Foster City

The Business Systems Analyst will partner with the Sr. IT BRM and Product Owner and key business functional leads to analyze and synthesize information, · understand the project context and deliverables, complete business analysis activities, · document and manage requirements, a ...

The resource should have 2-3 years of prior experience in a regulated cGMP environment. · Prior experience in the pharmaceutical /biotech sector is preferred. · ...

++Validation Test Lead with Life Sciences Domain Experience · + · +,+++ 10 years of Experience in Life Sciences, Computer System Validation and Testing · Must possess hands-on experience in Trackwise · Good understanding of FDA regulations, 21 CFR Part 11, GxP requirements along ...

The Business System Analyst will gather requirements and interface with IT and the vendor on issues and enhancements. · Gathering requirements. · Interfacing with IT and the vendor on issues and enhancements. · ...

This individual will perform the role of Application Administrator in the Quality Assurance department for Trackwise Documentum ComplianceWire applications. · They will perform daily business administrative tasks related to functional support of applications analyses tests deploy ...

A Validation Lead position is available with strong CSV exp at Net2Source Inc in Foster City CA. · Take ownership and lead validation activities. · Flexible and adaptive to change management. · ...

This is a job description for Veeva QMS Admin. The tasks will be centered around data/decisions necessary to configure the QMS workflows. Formal experience (and/or certification) in PM methodology is required. · Lead the implementation of Veeva QMS solutions for our clients. · Co ...

The role involves implementing Veeva QMS solutions for clients, including configuration and deployment activities. · Lead the implementation of Veeva QMS solutions for our clients,Provide training and support to end-users of the Veeva QMS system, · ...

This is a validation test engineer position with a company called Net2Source Inc. · ...

Meticulous Quality Assurance Auditor with over 5 years of experience leading QA/QC programs to drive strict compliance with diverse regulatory requirements. · Drive compliance with multiple regulatory requirements and company policies and procedures by auditing records and report ...

At LabAnswer, we are looking for a Business Analyst with expertise in clinical and commercial drug product lifecycle management using the Oracle Agile platform. · ...

Pharmaceuticals located in San Carlos is seeking a Quality Assurance Batch Record Reviewer / Person-In-Plant to support Quality oversight of manufacturing operations for the NIGHT SHIFT. · ...

The Manager Quality Assurance will report to Quality Assurance leadership and support GMP compliance related to drug substance and drug product manufacturing processes. · Support the development implementation and maintenance of GMP quality systems including policies procedures a ...

Neurona Therapeutics is a clinical-stage biotechnology company seeking an exceptional QA Manager to join our Quality Assurance (QA) team. · ...

We are seeking an exceptional candidate to join our Quality Assurance (QA) team. Our ideal candidate is a self-motivated individual who has a passion for QA and can thrive in a fast-paced dynamic environment. · Track, analyze, and report QA metricsReview and approval of facility ...

The Manager, Quality Assurance will report to Quality Assurance leadership and support GMP compliance related to drug substance and drug product manufacturing processes.This role will contribute to quality assurance activities ensuring compliance with applicable regulations and i ...

We are seeking an experienced Application Architect to lead the design, integration, and optimization of enterprise systems across EHS, Quality Management, and Product Lifecycle Management (PLM) domains. · ...

+At least 10 years of experience supporting and/or performing all aspects of computer systems validation activities including development of scalable validation strategies, documents, and perform document reviews · +At least 7 years prior experience in computer systems validation ...

We are seeking an experienced Application Architect to lead the design, integration, and optimization of enterprise systems across EHS, Quality Management, and Product Lifecycle Management (PLM) domains. · We'll work with visionaries across multiple industries to improve the hybr ...

This position provides support within the department and also throughout the business offering keen insight to process-related knowledge and manufacturing as related to data integrity computer system validation and technical engineering SOPs. · ...