Medical Device Developer
LGM grup
Total des années d'expérience :14 years, 9 Mois
SUPPORTED RESEARCH AND DEVELOPMENT EFFORTS TO CREATE NEW PRODUCTS, EQUIPMENT AND
PROCESSES.
COLLABORATED WITH LEADERSHIP TEAM TO IDENTIFY RELEVANT QUESTIONS AND DETERMINE BEST
METHODS OF COLLECTION.
PLANNED, MODIFIED, AND EXECUTED RESEARCH TECHNIQUES, PROCEDURES AND TESTS.
PERFORMED STATISTICAL, QUALITATIVE AND QUANTITATIVE ANALYSIS.
SCREENED PATIENT RECORDS, DATABASES AND PHYSICIAN REFERRALS TO IDENTIFY PROSPECTIVE
CANDIDATES FOR RESEARCH STUDIES.
DEVELOPED LOGICAL TECHNIQUES TO RESOLVE PROCESS PROBLEMS AND IMPROVE RESEARCH WORK.
Maximized customer satisfaction and business reputation by fabricating orthotics and prosthetic limbs meeting or
exceeding all company process standards, quality guidelines and technical directions.
Worked with vendors to source diverse materials and items for use during device fabrication processes.
Developed team communications and information for meetings.Increased customer satisfaction by resolving \[CT
Scan\] issues.
Developed team communications and information for meetings.Increased customer satisfaction by resolving \[CT
Scan\] issues.
Monitored manufacturing operations of electrical devices for compliance with safety protocols.
Wrote protocols, qualification documents, test plans and test reports for quality assurance purposes.
Developed internal processes and plans for mechanical verification, product development and factory processes.
Visited customer locations to evaluate requirements, demonstrate offerings and propose strategic solutions for
diverse needs.
Work experance
Researched state statutes, decisions, legal articles, codes and documents.
Researched and wrote contracts, agreements and proposals.
Explained available courses of action and possible repercussions of cases to clients.
Researched, wrote and filed all motions, writs and briefs for each case.
Formulated trial techniques specifically pertaining to each case.
- Irbid |