Responsibilities: Plan and execute design verification/stability engineering projects and reliability activities to support the development of safe and reliable medical devices. Develop and validate test methods, write protocols based on...
Responsibilities: Plan and execute design verification/stability engineering projects and reliability activities to support the development of safe and reliable medical devices. Develop and validate test methods, write protocols based o...
Responsibilities: Support daily manufacturing activities for clinical and commercial manufacturing programs. Execute and document batch records following Good Documentation Practices (GDP). Review and revise SOPs, batch records, and man...
Responsibilities: Support the planning, setup, and acquisition of external clinical data at the study level, assisting in managing study start-up, conduct, and closeout activities. Assist in creating external data transfer agreements, en...
Responsibilities: Follow established procedures, practices, and policies for functional units and the quality systems. Ensure adherence to regulatory business and department guidelines, policies, and procedures. Resolve sales order issu...
Responsibilities: Follow established procedures, practices, and policies for functional units and the quality systems. Ensure adherence to regulatory business and department guidelines, policies, and procedures. Resolve sales order issu...