Website Katalyst Healthcares & Life Sciences
Katalyst Healthcares & Life Sciences
Company : Katalyst Healthcares & Life Sciences
Roles & Responsibilities:
- Electronic Mechanical background.
- Demonstrated QMS experience along with documentation.
- Supplier Quality Management, Coordination and timely interaction.
- V&V protocols & reports.
- First Article Inspection experience.
- Once on boarded, resources will undergo extensive training on Philips' QMS along with product understanding and experience sessions.
- The scope of the requirement is to perform activities as below:
- Closure of open SICR's with CFT.
- Working with ME to complete FAI Plan & report for Telemetry CPE/NPI projects as defined by BU Priorities.
- Performing required tasks for the completion of AOS/EOL project as defined by BU priorities:
- Participating in change review analysis and planning.
- Own Part / Specification change and release including release EC.
- Define and review verification & Validation protocols/report.
- FAI: Develop Plan, Execute/Report review and documenting in database.
- Database details – Electronic Device Master Record (eDMR) explicitly customized to their Quality Management System. eDMR is integrated to SAP, Windchill etc.
- Provide first line of De fense for MX40 / SH1.0 Quality Issues (Part/Production).
- Providing support for determination & execution of MX40 repair & Exchange transfer.
- Generate project plans for PIE owned projects and assist list of deliverables for PMO/PDLM projects.
- Project management of MLD changes to the products.
- NPI – Monitor Release.