- Robert Half Office Team (Mahwah, NJ)
- …enhance the efficiency and effectiveness of documentation systems. * Support compliance with medical device regulations and quality assurance standards. * ... Description We are looking for a dedicated Regulatory Affairs Quality Assurance Specialist to...Solid understanding of quality assurance principles and regulatory requirements for medical devices. * Experience… more
- Integra LifeSciences (Plainsboro, NJ)
- …Canadian Medical Device Regulations, and other applicable regulatory agencies. Experience with assessing quality suppliers and purchasing specifications ... pathways to advance patient outcomes and set new standards of care. The ** Quality Compliance Specialist** will provide quality compliance support to the Collagen… more
- Sanofi Group (Morristown, NJ)
- …and bring hope to patients and their families. The strategic vision of Sanofi's Global Medical Device and Packaging organization is to lead the industry in ... market auto-injectors, pens, safety syringes, as well as connected medical device technologies, and we are gearing...equipment, printing, and vision control systems. + Knowledge of device and packaging regulations, quality systems, design… more
- Church & Dwight Co., Inc. (Princeton, NJ)
- …record + Transitioning to Generalist in at least 1 area: Consumer products, medical device , food, dietary supplements or pharmaceutical + Contributions focused ... QMS Head (change control, document control/training, CAPA, validation), the Global Quality Area Head is responsible for leading the development and implementation… more
- Integra LifeSciences (Princeton, NJ)
- …medical devices in conformance with the Quality System Regulation, ISO 13485, Medical Device Directive, ISO 14971, IEC 60601 and other regulatory ... improve processes and procedures. + Collaborate with External Manufacturers during regulatory audits and inspections. + Support Supplier Quality projects… more
- Integra LifeSciences (Princeton, NJ)
- … mindset, a willingness to learn about sterilization and microbiology, an understanding of medical device quality systems, and a commitment to ensuring ... teams to ensure sterilization processes are integrated into the overall supplier quality process. ** Regulatory Compliance & Documentation:** + Ensure thorough… more
- Integra LifeSciences (Princeton, NJ)
- …Sigma, or Change Management (eg, Prosci, ADKAR). + Prior experience in the medical device or highly regulated industry. **Core Competencies:** + Strategic ... Development, Talent Development, or Organizational Effectiveness. + Strong knowledge of Quality and Regulatory Compliance environments. + Experience building or… more
- Actalent (Basking Ridge, NJ)
- …Microsoft Office programs (Word, Excel, PowerPoint, Outlook). + Knowledge of global medical device labeling requirements. Additional Skills & Qualifications + ... Job Title: Quality Associate Job Description The Quality ...procedures. The role involves coordinating labeling projects to ensure regulatory compliance and providing guidance to team members on… more
- Terumo Medical Corporation (Somerset, NJ)
- …Corporation (TMC) develops, manufactures, and markets a complete, solutions-based portfolio of high- quality medical devices used in a broad range of applications ... drive clear economic value, better clinical outcomes and improved quality of life for patients. TMC is part of...of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in… more
- Merck (Rahway, NJ)
- …the organizations (our Manufacturing Division/our Research & Development Division) such as Quality , Regulatory CMC, and technical functions, to ensure timebound ... of integration and partnering for Pharmaceutical development/ CMC with Quality , Regulatory , Operations, Non-clinical, Clinical, and other functional… more