design quality engineer à Oberdorf

publié
contact
Olivier Worch, Bâle Professionals Health Care & Life Sciences
type d'emploi
temporary
postuler >

job details

publié
lieu
oberdorf, nidwalden
secteur
Life Sciences
type d'emploi
temporary
référence
11683
contact
olivier worch, bâle professionals health care & life sciences
téléphone
058 201 55 50
postuler >

description du poste

Randstad Professionals is currently looking for a EDesign Quality Engineer (Medical device/Power tools) ) who will be assigned an interesting challenge for a major client based in SOlothurn.   This contract is an unique opportunity to join a major client, global group focusing on the Healthcare sector  (Medical device, Pharma/vaccines, Consumer health).

The initial assignment will October/November and will initially last until  March 2019.

 

Job description:

• Design Quality team member focused on life cycle management activities.  • Enhance the Design Control/Risk Management processes to better reflect state of the art practices and drive continuous improvement.  • Apply statistical methods and process/design excellence tools to establish test plans, evaluate test data and processes. Perform Gage R&R studies.  • Conduct and lead design verification and validation activities.  • Conduct and lead design / process failure mode effects and analysis.  • Provide leadership in all areas of the Quality System (CAPA,Complaints, NC, Risk Management)  • Provide expertise with regulations to other disciplines.  • Responsible of clear definition of project scope and deliverables, milestones and timeline, project risks and contingency plans.  PROFESSIONAL EXPERIENCE REQUIREMENTS  • A minimum of a Bachelor’s degree in Engineering or related technical or scientific discipline with a minimum of 5 years of experience in related field is required.  • Proven exceptional written and oral presentation skills  • Working knowledge of Design Controls, GMPs, QSR, 21 CFR 820, MDD 93/42/EEC, ISO13485/ISO14971 quality requirements is required.  • Previous Quality Engineering experience is preferred.  • Experience in a Medical Device regulated environment  OTHER REQUIREMENTS  • Knowledge with Medical device / Power Tools  • Excellent problem solving, decision-making, and root cause analysis skills are required.  • Strong quality engineering skills with a proven track record in design verification/validation, process verification/validation, and design/process Failure Mode and Effects Analysis is preferred.  • Working knowledge of material science and mechanical product knowledge is preferred.

• Development and manufacturing experience is preferred. 

 

If you are interested for this great role, don't hesitate to send your application or to contact me directly.  I am looking forward to sharing the project details with you. 

Olivier Worch Consultant Life Sciences T +41 58 201 55 55 olivier.worch@ch.randstad.com