Website Katalyst Healthcares & Life Sciences
Katalyst Healthcares & Life Sciences
Company : Katalyst Healthcares & Life Sciences
Responsibilities :
Author and Review existing Design History Files, identify scope, and mark gaps where necessary documents are missing.
Utilize Vault Systems to manage Document workflow.
Generate or analyze and update existing risk documentation (DFMEA or risk tables).
Coordinate, prepare, and conduct design reviews with cross-functional teams.
Perform functional relationship analyses (FRA) and tolerance stack-ups.
Generate comprehensive protocols to test/analyze the product for design verification and design validation (V&V).
Update prints and other design and manufacturing elements.
Requirements:
B.S. degree from an ABET accredited school (or global equivalent) in Biomedical, Mechanical, or Materials engineering, or equivalent.
Familiarity with Vault Systems.
Familiarity with drafting standards and geometric dimensioning and tolerancing (GD&T).
Strong Background in DHF documentation authoring and executing for Medical Devices.
Ability to effectively work within a team to expedite completion of critical project tasks with cross functional groups including Regulatory and Quality.
Establishing a process method which meets performance and quality requirements.
Ability to give clear and concise oral presentations.
Technical writing.
Microsoft Office Suite.
Previous system experience with Vault.
Excellent communication, teamwork, and organizational skills are essential.
Candidates must be self-starters and self-motivators.
B.S. degree from an ABET accredited school (or global equivalent) in Biomedical, Mechanical, or Materials engineering, or equivalent.