Associate Director, GLP/GCP Quality Audits and Compliance - Princeton

The Senior Manager Quality Audits is responsible for leading internal external audits across Acadia's portfolio ensuring compliance with GMP regulations maintaining robust quality agreements supporting quality management system effectiveness.Plan coordinate schedule conduct inter ...

The Associate Director plays a critical role in protecting data integrity and regulatory readiness across the company's nonclinical and clinical portfolio.This position leads the planning execution and reporting of internal external GLP GCP audits ensuring compliance with U.S int ...

We're Fiserv,a global leader in Fintech and payments,and we move moneyand informationin a way that moves the world.We connect financial institutions,corporations,merechantsand consumers to one another millions of timesa day - quickly,reliably,and securely.Any time you swipe your ...

+Legend Biotech is seeking an Associate Director Compliance Risk Audit Monitoring for its Compliance team in Somerset NJ. · ++Develop Conduct Compliance Risk Assessments Identify evaluate inherent residual compliance risks business units functions Coordinate cohesive approach ali ...

Legend Biotech is seeking an Associate Director, Compliance Risk, Audit and Monitoring as part of the Compliance team based in Somerset. · ...

+Job Summary · Legend Biotech is seeking an Associate Director to oversee corporate compliance risk assessment audit monitoring activities. · +ResponsibilitiesDevelop Implement Conduct Compliance Risk Assessments: Identify evaluate inherent residual compliance risks across busine ...

Legend Biotech is seeking an Associate Director, Compliance Risk, Audit and Monitoring as part of the Compliance team based in Somerset NJ. · ...

+ Inspection Readiness Lead at Made Scientific:JOB SUMMARY+ The Inspection Readiness Lead (Associate Director) is responsible for establishing, maintaining, and continuously improving a state of inspection readiness across GMP cell therapy operations.+ · + ++Design, implement, a ...

This role supports the Market Research (MR) Compliance and Operations Team under direction and guidance from the MR Compliance Lead. · The Coordinator works cross-functionally supporting Analytics activities related to Market Research and GVP Activities to ensure that internal au ...

As an NRG employee, we encourage you to take charge of your career and development journey. · We invite you to explore exciting opportunities across our businesses..Your growth is key to our ongoing success—take the lead in shaping your career development, goals and future · Supp ...

The Inspection Readiness Lead (Associate Director) is a quality leader responsible for establishing and maintaining inspection readiness across GMP cell therapy operations from clinical through commercial stages. · Design, implement and sustain multi-site inspection readiness pro ...

++Examine and evaluate internal IT controls.+ · +Perform IT audits that are objective.+Maintain professional standards to include independence.+Produce deliverables such as test scripts and evidence in a timely fashion.+Communicate audit results in a clear and concise manner., ...

We ae seeking a Quality Assurance Director to oversee Quality Assurance services for New Jersey and Maryland.The Regional Quality Assurance Director is responsible for the overall compliance, quality assurance, and oversight of policies and procedures in the assigned States under ...

Community Options is seeking a Quality Assurance Director to oversee quality assurance services for New Jersey and Maryland. · Assist in the development of QI plans. · Assess processes and outcomes. · Monitor policies and procedures. · ...

Guerbet is looking for a qualified QA Manager to enhance their quality management system through comprehensive SOP development and review. The ideal candidate will have excellent communication skills and be able to work independently as part of a team. · ...

The Associate Director Clinical Quality develops implements manages quality aspects companys clinical development ensuring that activities including those conducted by outsourced partners comply Good Clinical Practice GCP regulations internal Standard Operating Procedures SOPs re ...

We are conducting a search for a talented and knowledgeable Technology & Operations Risk Analyst to focus on identifying, mitigating, and reporting risks related to the development and operation of exchange trading systems, · as well as the supporting infrastructure and operation ...

We are passionate about hiring innovative thinkers who believe in the promise of education and lifelong learning. We are energized by cultivating growth, innovation, and continuous transformation for the next generation of rising professionals as leaders.This position will report ...

Guerrbet is looking for a qualified QA manager to enhance our quality management system through comprehensive SOP development, · review, and revision.Guerbet is a global leader in medical imaging offering an extensive portfolio of pharmaceuticals, · medical devices digital soluti ...

The Company Munich Re America Services (MRAS) is a shared service organization that delivers services to all Munich Re US P&C Companies and other group entities. We're adding to our diverse team of experts and are looking to hire those who are committed to building a culture that ...