Associate Director, Clinical Quality Management - Princeton, NJ

We're a company that genuinely cares about our people, our products, our consumers and the environment. · A place where you can make a real difference. · United by the belief that when we strive for growth, · anything is possible. · We have a unique culture courage, · determinati ...

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. · ...

We're a company that genuinely cares about our people, our products, · our consumers and the environment. · ...

This Manager Quality Compliance & Continuous Improvement supports continuous improvement initiatives within the Quality Management System. It oversees quality activities in alignment with cGMPs SOPs and regulatory requirements collaborates with Corporate Quality and cross-functio ...

The Manager, Quality Systems is responsible for the design, implementation, maintenance, · and continuous improvement of global quality systems that support compliance, · operational excellence, · and risk mitigation across the pharmaceutical product lifecycle. · ...

We're a company that genuinely cares about our people, our products, our consumers and the environment. United by the belief that when we strive for growth, anything is possible. · A collective energy and ambition. · A place where you can make a real difference. · ...

We are seeking a Manager Product Quality to join our Quality organization. This position will be located in Ewing NJ and operates on a hybrid basis.This role is responsible for supporting the strategic direction development and execution of quality and compliance policies process ...

The Manager Quality Systems is responsible for designing implementing maintaining and continuously improving global quality systems that support compliance operational excellence and risk mitigation across the pharmaceutical product lifecycle. · Bachelor?s degree in Life Sciences ...

We're a company that genuinely cares about our people, our products, our consumers and the environment. · Support and execute quality and compliance strategy for the business · Ensure effective communication of quality issues · ...

The Quality Associate tasks include: CW shadows ongoing studies and supports them to provide Quality oversight and recommend best practices. · Consults on major and critical quality issues with Senior GCP Level 1 members. · Supports risk assessments for the annual GQM Audit Plan. ...

The Quality Control Manager will lead product-focused quality control operations to ensure all finished goods meet established specifications, regulatory requirements, and internal quality standards. · ...

Joining us is a chance to do important work that creates change and shapes the future of healthcare. · ...

· Support Clinical Trial Teams in developing Risk Assessment Mitigation Plans identifying critical-to-quality factors Parameters with Quality Tolerance Limits Key Risk Indicators thresholds monitoring tactics · Closely collaborate with relevant vendors ensure proper implementati ...

We are seeking a Managing Consultant with air quality compliance & permitting consulting experience to join our Environment & Health Division. As part of this role, you will critically review and interpret local, state, and federal environmental regulations with focus on air comp ...

We invite you to contribute to a more sustainable future working in an open collaborative and empowering company combining local experience with global knowledge we together shape the societies of tomorrow. · ...

We are seeking a Managing Consultant with air quality compliance & permitting consulting experience to join our Environment & Health Division. As part of this role, you will be responsible for critically reviewing and interpreting local, state, and federal environmental regulatio ...

We are seeking an experienced RBQM Specialist to play a key role in shaping how we design, monitor and deliver our clinical trials. · ...

This position is responsible for developing Quality and NAO strategic objectives and strong business understanding of the value chain and customer focus, for supporting and upholding processes anchored in the Novo Nordisk Quality Management System across NAO thereby ensuring high ...

This position is responsible for leading all aspects of Quality Management Clinical Operations & Audit and Quality Management Performance Reporting. · ...

This position is responsible for developing Quality and NAO strategic objectives and strong business understanding of the value chain and customer focus. The role also involves supporting quality processes anchored in the Novo Nordisk Quality Management System across NAO to ensur ...

The Clinical Medical and Regulatory CMR department at Novo Nordisk is one of the most diverse and collaborative groups within the organization From healthcare provider interactions and developing implementing regulatory strategies with the FDA to providing medical education colle ...