Senior Manager of Regulatory Affairs and Quality Assurance - (Medical Device) - Hybrid in MA. Our client is a growing boutique IVD and Medical Device company and they are seeking a Senior Manager of Regulatory Affairs and Quality Assurance to lead a small international team to ensure compliance with...
Bachelor's degree in a scientific discipline and 3 to 7 years' experience in the pharmaceutical or biotech industry with 2 to 5 years in Clinical Quality Assurance. ...
The Senior Clinical Quality Assurance Manager leads the Clinical Quality team for the Endoscopy and Urology divisions. ...
Years Quality Assurance experience in a Food Production Manufacturing plant. ...
Years Quality Assurance experience in a Food Production Manufacturing plant. ...
The Senior Clinical Quality Assurance Manager leads the Clinical Quality team for the Endoscopy and Urology divisions. ...
We are looking for a Quality Assurance Manager. Profil recherché pour le poste : Quality Assurance Manager. Develop and execute comprehensive and specific Quality Assurance plans to O&M scope of services. ...
Bachelor’s degree in a scientific discipline and 3 to 7 years’ experience in the pharmaceutical or biotech industry with 2 to 5 years in Clinical Quality Assurance. ...
The Senior Clinical Quality Assurance Manager leads the Clinical Quality team for the Endoscopy and Urology divisions. ...
Bachelor’s degree in a scientific discipline and 3 to 7 years’ experience in the pharmaceutical or biotech industry with 2 to 5 years in Clinical Quality Assurance. ...
As a registered member of the Public Company Accounting Oversight Board (PCAOB), the Firm adheres to the highest professional standards and provide a full range of assurance services. ...
Reporting to the Corporate VP QA/RA, the Global QA/RA Systems Manager is responsible for providing leadership, planning, project coordination, and management to develop a cost-effective electronic Quality Management Systems (eQMS) and harmonized QA/RA information systems while concurrently facilitat...
The ideal candidate will have a strong background in aerospace engineering, quality assurance principles, and manufacturing processes. Regularly interface with Program Management, Engineering, Operations, and Customers to ensure understanding, documentation, flow-down, and implementation of CPI Rada...
Objectives involve ensuring patient and employee safety and the achievement of customer quality requirements, create, monitor and improve quality systems/programs, reduce quality costs and maintain compliance within FDA and ISO regulations for + $500 million in annual sales. Oversee and implement an...
Reporting to the Director, R&D GLP/GCLP Quality, located in Norwood, MA, the Manager of Good Laboratory Practice/Good Clinical Laboratory Practice (GLP/GCLP), applies established knowledge and experience in internal, in-process, study and vendor audits. The Manager will also partner with R&D to crea...
The Quality Assurance (QA) Compliance Specialist I performs compliance activities in support of production, engineering ensuring all activities are performed according to internal Quality System requirements, cGMP, FDA and ISO 13485 standards. Provide quality assurance support of investigations incl...
We are looking for an experienced Quality Engineer to join the Devens, MA site. Quality Engineer in the healthcare industry. Understanding customer requirements and implementing appropriate controls, documentation, action plans, and tools necessary to perform quality related tasks at all phases with...
The Quality Assurance Specialist will play a crucial role in supporting various areas within UGT Quality Assurance, ensuring compliance with Good Manufacturing Practices (GMP) and maintaining high standards of documentation. Our client is seeking a detail-oriented and knowledgeable Quality Assurance...
The Quality Control Manager for Biologics is responsible for managing the quality control processes for biologics products, ensuring their integrity and compliance from development to production. Develop, implement, and maintain quality control systems and protocols for biologics. Work closely with ...
Our client is seeking a Quality Manager to join their growing team. The Quality Manager is responsible for the implementation of new customer processes, including design and development of production fixtures and workflow documentation. ...
Reporting to the Associate Director, QA Drug Product, the QA Sr. The QA Manager will play a crucial role in executing the operational strategy while adhering to regulatory compliance and quality standards. Manager, Drug Product Operations is responsible for coordinating and executing the quality and...
Design Quality Assurance Engineer III. At Boston Scientific, the Design Quality Assurance Engineer III directly supports medical device product development from concept through commercialization. Serves as a Quality representative to improve awareness, visibility, and communication on quality initia...
Provide training and support for the Quality Management System; Quality systems, policies, procedures, and core processes. Plan, execute, and oversee inspection and testing of products in coordination with the Quality Technician to verify conformance with specifications and deliverables. Assist oper...
The Manager of Quality Audits will manage the Quality Systems, Audit and Compliance program and be responsible for the Self-inspection/Internal Audit and coordination of the External Audit processes, to ensure all ElevateBio’s processes and systems are in compliance with internal policies and proced...
Senior Director of Quality, Regulatory and Clinical Affairs. Key leadership position for Quality, Regulatory and Clinical activities in support of the In Vitro Diagnostic Clinical business. The role will be responsible to work through multiple levels within the organization and external stakeholders...