Sr. Manager, QMS Governance - Durham

We are seeking a dynamic Practice Leader to build, scale, · and lead our CCaaS practice with deep expertise in Genesys Cloud CX.Own delivery governance and oversight across Genesys Cloud CX · and Genesys WEM. · Owning P&L responsibility for the Genesys delivery practice. · ...

The Quality Systems team is responsible for establishing and continuously improving the Quality Management System (QMS) that supports the site and Global Compliance activities ensuring systems and business processes are robust, effective, and efficient to comply with required reg ...

We are seeking a dynamic Practice Leader to build scale and lead our CCaaS practice with deep expertise in Genesys Cloud CX including enterprise-grade routing omnichannel orchestration workforce engagement analytics and native AI capabilities. · Building our Company · ...

The QA/RA Manager will develop and continuously improve all facets of the Quality Management System in accordance with global regulatory requirements. · 10+ years of QARA experience in software medical device regulated industry. · Strong working knowledge of Quality Management Sy ...

We are recruiting IRT Leads to oversee our Interactive Response Technology (IRT)/ Randomization & Trial Supply Managment (RTSM) systems that manage randomization, drug supply and site/subject activities for clinical studies. In this role you will support study teams through the f ...

Beam is seeking a highly skilled Specialist I/II to join our growing Digital Quality & Data Integrity team and play a pivotal role in shaping the future of digital compliance. · Oversee risk-based Computerized System Validation (CSV)/Computerized Software Assurance (CSA) activiti ...

This is a strategic leadership role responsible for driving enterprise-wide IT compliance, governance, and quality assurance across the Diagnostics and BLS business units. · ...

Labcorp is hiring an Executive Director IT Quality Compliance. This is a strategic leadership role responsible for driving enterprise-wide IT compliance governance quality assurance across Diagnostics BLS business units.This hybrid position offers a balanced schedule of minimum t ...

The Compliance and Training Manager will provide expertise in training design and execution for Beam Therapeutics. This role is responsible for developing, implementing, and administering global training while supporting the application of Global Quality Policies & Standards. · D ...

This is a strategic leadership role responsible for driving enterprise-wide IT compliance, governance and quality assurance across the Diagnostics business units. · 10+ years' experience in an FDA regulated industry. · Bachelor's Degree required. · ...

The Senior SAP IT Program Manager leads complex global SAP S/4HANA implementation and migration initiatives within a highly regulated pharmaceutical environment. This role ensures successful delivery of SAP enhancements and bug fixes in compliance with FDA GxP SOX and data integr ...

The Manager/Sr. Manager, Compliance and Training will provide expertise in training design and execution for Beam and support overall training management. · Develops, leads, · & implements training initiatives that are aligned with business strategies. · Designs digital · & physi ...

Kincell Bio engineers cells into therapies. · We offer challenging career opportunities, competitive benefits,and an environment that recognizes and rewards performance.Kincell is seeking a highly motivated Manufacturing Specialist who will be a key contributor to a dynamic and c ...

+ Job summary:Job summary · Kincell Bio engineers cells into therapies. With manufacturing facilities located in Research Triangle Park, NC and Gainesville, FL, Kincell Bio is a contract development and manufacturing organization (CDMO) with the mission to streamline CMC developm ...

Kincell Bio is a contract development and manufacturing organization (CDMO) with the mission to streamline CMC development, apply expertise in analytical and process development and GMP manufacturing, testing and release from early clinical to pivotal studies and product launch. ...

The Clinical Quality Operations Manager is responsible for overseeing the strategic implementation of quality by design principles in assigned clinical trials. They will be the single point of contact for clinical trial teams for all activities associated with risk-based quality ...

The Quality Associate Director/GMP Lead Site Auditor will have leadership responsibility for the site internal audit program. · Actively manage site auditors to ensure performance contributes to effectiveness of site audit program · Function as change agent related to culture and ...

+Job summary · The Quality Associate Director/GMP Lead Site Auditor will have leadership responsibility for the site internal audit program. · +Actively manage, mentor, and support site auditors · Function as a change agent related to culture and audit program performance · ...

The Quality Associate Director/GMP Lead Site Auditor will have leadership responsibility for the site internal audit program encompassing the full scope of site operations. · - Actively manage mentor and support site auditors to ensure performance of auditors contributes to effec ...

The Quality Associate Director/ GMP Lead Site Auditor will have leadership responsibility for the site internal audit programThe role requires ability to lead and perform operational aspects of audit program apply risk-based principles communicate results to stakeholders evaluate ...