International Technidyne Corp Work Values

Daily Duties at International Technidyne Corp:

Senior Scientist with a distinguished twenty-plus year professional career in planning and project-managing testing and quality management initiatives supporting the development of medical devices and diagnostic assays. Industry background supplemented and enhanced by experience in educating students. Core competencies include: • Verification/Validation Studies • Resource Allocation • Project Management • Study/Master Test Planning • Protocol Development • Standard Operating Procedures (SOPs) • Data Equivalence Testing • User Acceptance Testing (UAT) • Reliability Testing • Stability Testing • Alpha Clinical Protocols • Good Manufacturing Processes (GMPs) • Product-Process Risk Assessment • Quality Control/Management • Quality System Regulatory Compliance • High-Performance Team Building • Training/Development • Information Management A creative, motivated analyst, communicator, facilitator, and leader with a resolute detail orientation, the unique ability to communicate and collaborate with scientific and management personnel, and a verifiable record of achievement in employing diverse resources in the timely completion of projects and attainment of objectives.

What they like about International Technidyne Corp:

Working for a company with an emphasis on social values and helping society is a clear and important priority for you - a critical factor in who you choose to work for. In contrast to other factors, you place an organization's reputation for fairness and concern for the community above most other aspects of the company. As you search for a new job opportunity, it is usually possible to find out if the company is involved in the community and/or if it is addressing problems and issues in society. Pay special attention to non-profit organizations and those specifically involved in social action. Moreover, speaking with current and former employees should enlighten you to perceptions of the fairness of the company's leaders and the treatment of employees.

Tags

Product Quality Support, Product stability , medical device software validation, adjunct professor_biology

Skills

Software Verificaion and Validation, Writing Standard Operating Procedures, Conducting Training across technical support staff, sales and marketing staff and external vendors, Completing Technical File submissions for Regulatory compliance, Developing and executing validation protocols and scripts for medical devices, diagnostic tests, and software, knowledge of Good Manufacturing Process (GMP) documentation including master device records and device history records as well as quality system regulations under FDA 21 CFR Part 820, 801, and 809; ISO 10005-2005, 18113-2009, and 15223-1; and I.S. EN 1364, Phlebotomist, Writing and reviewing product specification documents and product labeling including package inserts, box labeling, operator manuals, and training guides.

These are some of the questions we asked our climbers about their experiences with International Technidyne Corp: