Supplier Quality Engineer in Zuchwil

veröffentlicht
Kontakt
Olivier Worch, Basel Professionals Health Care & Life Sciences
Jobtyp
Temporary
jetzt bewerben

job details

veröffentlicht
Ort
Zuchwil, Solothurn
Sektor
Life Sciences
Jobtyp
Temporary
Referenznummer
12477
Kontakt
Olivier Worch, Basel Professionals Health Care & Life Sciences
Telefon
058 201 55 50
jetzt bewerben

Stellenbeschreibung

Randstad Professionals is currently looking for a Supplier Quality Engineer / validation Consultant  (German speaker) who will be assigned an interesting challenge for a major client based close to Solothurn.

This contract is an unique opportunity to join a major client, global group focusing on the Healthcare / Medical device sector. The initial assignment will start immediately and will last until December 2019

 

Contract details:

Start Date:   01/04/2019

Requisition End Date:   31/12/2019

 

Assignment overview

To ensure all externally manufactured products meet new EU MDR requirements.

Collaborate with suppliers to obtain details for manufacturing process information, production risk management and direct part marking.

This information will be used to update the product’s technical file to be in compliance with Medical Device Regulations.

 

Accountability Description

The EU MDR SQE will evaluate the supplier’s manufacturing process information, production risk management, direct part marking documentation against MDR Requirements; collaborate with the supplier to revise existing or develop new manufacturing process information, production risk management and/or direct part marking documentation as applicable.

You will become a member of the technical file remediation efforts to ensure externally manufactured products meet EU MDR requirements. This includes supporting project deliverables; meeting project timelines; resolving identified supplier issues and executing the overall project related to technical file remediation requirements.

• Assess supplier drawings and process information to support project deliverables:

  - Direct part marking documentation

  - Manufacturing Process Information

  - Production risk management file

  - Validation protocols and reports

• Work with Suppliers to meet EU MDR requirements and resolve issues with obtaining Supplier Product information.

• Cross coordinate Workstream activities/interdependencies with other workstream and project teams.

• Partner with Supply Chain to support EU MDR supplier communications and rollout of EU MDR

 

Supply Chain Workstream activities;

• Support definition and clarification of EU MDR supplier related process requirements.

• Support Review and Approval EU MDR Change Projects

• Support Supplier Quality Functional Impact Assessments

• Support Review and Approval of supplier Process Validation Protocols and Reports as applicable.

• Support the update of supplier related Inspection Criteria

 

PROFESSIONAL EXPERIENCE REQUIREMENTS:

• 3 years  as Project Engineer, Quality Engineer, Project Manager or equivalent role

within regulated industry.

• 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.

• ISO-13485 and FDA QSR is required.

• Excellent organizational skills and attention to detail is required

• Demonstrated ability to effectively define, plan and manage projects

• Proven exceptional written and oral presentation skills

• Experience with systems implementation/rollout projects preferred

 

EDUCATIONAL REQUIREMENTS:

A minimum of a bachelor’s degree or equivalent in engineering or associated technical field is required. A minimum of 3 years’ experience in a quality engineering is required.

OTHER REQUIREMENTS:

• Understanding supplier validation procedures and execution.

• Strong Project Management skills, must understand the critical path, identify program resources,

setup project plan and track execution, establish project structure and governance around critical projects.

• Experience with GD&T, Inspection Methods, and Drawing Review/Approval.

• Experience working with suppliers across multiple sites and business centers.

• Process Excellence Black Belt or Master Black Belt

• Must be highly organized, creative, articulate and analytical

 

If you are interested to learn more about this great opportunity, don’t hesitate to get in touch with me. Feel free to send me your CV at following email

olivier.worch@randstad.ch

I am looking forward to receiving your applications