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Quality Supplier Engineer
Eingestellt von Michael Bailey Associates - Zurich
Gesuchte Skills: Support, Engineering, Engineer
Projektbeschreibung
Supplier Quality Engineer- 11 months contract Switzerland
The project goal is to ensure all product technical file contributions meet new EU MDR requirements.
Tasks:
Develop project goals, deliverables and plans for execution in 2019 inclusive of the following Workstreams:
. Packaging
. Partner with EU MDR Supply Chain Workstream Core Team to support tracking and expediting of supplier related product codes to meet project deadlines
. Support definition and clarification of EU MDR supplier related process requirements.
. Support Review and Approval EU MDR Change Projects as applicable.
. Support Supplier Quality Functional Impact Assessments as applicable.
. Support Review and Approval of supplier Process Validation Protocols and Reports as applicable.
. Support the update of supplier related Inspection Criteria as applicable.
. Other related tasks may be assigned at the discretion of local Supplier Quality Management and/or the EU MDR Supply Chain Workstream Core Team (SQ Lead).
EDUCATION & EXPERIENCE REQUIREMENTS:
A minimum of a Bachelor's degree or equivalent in Engineering and/or Technical Field is required.
A minimum of 3 years' experience in a supervisory capacity is required.
A minimum of 2+ years of experience in a medical device and/or pharmaceutical industry is required.
Familiarity with ISO-13485 and FDA QSR is required. Excellent organizational skills and attention to detail is required.
Must be able to work independently and prioritize with limited supervision.
Strong written and oral communication and interpersonal (listening) skills.
Please send your CV
Michael Bailey International is acting as an Employment Business in relation to this vacancy.
The project goal is to ensure all product technical file contributions meet new EU MDR requirements.
Tasks:
Develop project goals, deliverables and plans for execution in 2019 inclusive of the following Workstreams:
. Packaging
. Partner with EU MDR Supply Chain Workstream Core Team to support tracking and expediting of supplier related product codes to meet project deadlines
. Support definition and clarification of EU MDR supplier related process requirements.
. Support Review and Approval EU MDR Change Projects as applicable.
. Support Supplier Quality Functional Impact Assessments as applicable.
. Support Review and Approval of supplier Process Validation Protocols and Reports as applicable.
. Support the update of supplier related Inspection Criteria as applicable.
. Other related tasks may be assigned at the discretion of local Supplier Quality Management and/or the EU MDR Supply Chain Workstream Core Team (SQ Lead).
EDUCATION & EXPERIENCE REQUIREMENTS:
A minimum of a Bachelor's degree or equivalent in Engineering and/or Technical Field is required.
A minimum of 3 years' experience in a supervisory capacity is required.
A minimum of 2+ years of experience in a medical device and/or pharmaceutical industry is required.
Familiarity with ISO-13485 and FDA QSR is required. Excellent organizational skills and attention to detail is required.
Must be able to work independently and prioritize with limited supervision.
Strong written and oral communication and interpersonal (listening) skills.
Please send your CV
Michael Bailey International is acting as an Employment Business in relation to this vacancy.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Ingenieurwesen/Technik, Sonstiges