Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
Medical Device Senior Technical Expert - Quality Engineer
Eingestellt von Michael Bailey Associates - UK Contracts
Gesuchte Skills: Engineering, Design, Engineer
Projektbeschreibung
For our Life Sciences client in Switzerland, we care seeking for a Medical Device Senior Technical Expert - Quality engineer.
JOB TITLE: MEDICAL DEVICE TECHNICAL EXPERT - QUALITY ENGINEER
START DATE: 27/01/2017
END DATE: 30/06/2017
LOCATION: BASEL, SWITZERLAND
LANGUAGE: Excellent skills in English language are required.
YOUR EXPERIENCE:
Education:
Master degree in Science/Engineering or Mechanical Engineering or University level engineering education.
Professional Experience:
The successful candidate for this position will support technical activities within the development of parenteral delivery systems, eg drug/device combination products and medical devices.
An ideal candidate would have a relevant degree in engineering and at least 5 years of experience in a similar area, including:
- Pre-filled-syringe device development, from early phase activities up to commercialization and production scale-up;
- Medical device quality assurance;
- DHF compilation, including Design Control process and other applicable regulatory, QA and GMP aspects;
- Understanding of medical device regulations (FDA 21CFR 820, EU Medical Device Directive);
- Background in mechanical engineering in general
- Product design/Design for manufacture
- Test and verification, incl. development of methods and equipment
- Experience in medical device quality assurance;
- Good communication and conflict solving skills;
- Good technical knowledge in primary containers, eg syringes and cartridges;
- General understanding of pharmaceutical development ;
- General understanding of Human Factors Engineering and Risk management.
YOUR ROLE:
Main Tasks:
- Ensure product compliance for the assigned projects
- Compile Design Control documentation and contributing to a high quality Design History file.
- Establishes/Participates in the documentation strategy
We welcome applications of consultants' who match most of the above requirements and are available on a short notice. There is a competitive Hourly rate available for the contract; alternative market rates are also welcome.
We hope that the role will be of interest to you and understand that further information may be required prior to an application to the end client, please feel free to email or call me at anytime with any questions you may have.
Looking forward to hear from you soon,
Kind regards,
Neha Sharma
Pharmaceutical & Life Sciences Business Developer
Recruiting Team MBA,
Michael Bailey Associates
Michael Bailey International is acting as an Employment Business in relation to this vacancy.
JOB TITLE: MEDICAL DEVICE TECHNICAL EXPERT - QUALITY ENGINEER
START DATE: 27/01/2017
END DATE: 30/06/2017
LOCATION: BASEL, SWITZERLAND
LANGUAGE: Excellent skills in English language are required.
YOUR EXPERIENCE:
Education:
Master degree in Science/Engineering or Mechanical Engineering or University level engineering education.
Professional Experience:
The successful candidate for this position will support technical activities within the development of parenteral delivery systems, eg drug/device combination products and medical devices.
An ideal candidate would have a relevant degree in engineering and at least 5 years of experience in a similar area, including:
- Pre-filled-syringe device development, from early phase activities up to commercialization and production scale-up;
- Medical device quality assurance;
- DHF compilation, including Design Control process and other applicable regulatory, QA and GMP aspects;
- Understanding of medical device regulations (FDA 21CFR 820, EU Medical Device Directive);
- Background in mechanical engineering in general
- Product design/Design for manufacture
- Test and verification, incl. development of methods and equipment
- Experience in medical device quality assurance;
- Good communication and conflict solving skills;
- Good technical knowledge in primary containers, eg syringes and cartridges;
- General understanding of pharmaceutical development ;
- General understanding of Human Factors Engineering and Risk management.
YOUR ROLE:
Main Tasks:
- Ensure product compliance for the assigned projects
- Compile Design Control documentation and contributing to a high quality Design History file.
- Establishes/Participates in the documentation strategy
We welcome applications of consultants' who match most of the above requirements and are available on a short notice. There is a competitive Hourly rate available for the contract; alternative market rates are also welcome.
We hope that the role will be of interest to you and understand that further information may be required prior to an application to the end client, please feel free to email or call me at anytime with any questions you may have.
Looking forward to hear from you soon,
Kind regards,
Neha Sharma
Pharmaceutical & Life Sciences Business Developer
Recruiting Team MBA,
Michael Bailey Associates
Michael Bailey International is acting as an Employment Business in relation to this vacancy.
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Medien/Design, Ingenieurwesen/Technik