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:

A hiring company that offers alternative approaches to pay, performance bonuses, and/or equity in the firm is very attractive to you. You're generally less interested in working for an organization offering only traditional, salary-based compensation, one with limited opportunity to acquire equity in the firm, or one that does not actively promote skill development. In addition, you are more likely to choose a company that offers a variety of internal career options, with defined career paths. You view the learning of new skills and development of your expertise as key to your career advancement. These aspects of an organization may become even more important to you as you progress in your field, and are especially critical if you change career or occupation.

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: