This is a contract, per-project role, each project is scoped according to the needs of the SMEs.
ensures that all system-level project / program work products (e.g., plans, requirements, specifications, tests, test results, traceability, risk management documents, reports) meet quality, reliability, and compliance requirements for medical technology (ISO13485, IEC62304, 82304, FDA CFR Part 11, GDPR requirements).
Planning, developing and implementing verification / validation plans/protocols, including scripting scenarios.
Reviewing all project / program work products (e.g. plans, requirements, specifications, code reviews, tests, test results, traceability, risk management documents, reports).
Provide software design and architecture suggestions to improve product Quality
Drive clarity and consistency in documentation
price is just an indicator, so have to be discussed
must be based in Germany or Thailand
About the recuiterMember since Aug 27, 2017 Dave Weasel
from Bergamo, Italy