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 - Testing, Switzerland
Eingestellt von Michael Bailey Associates - UK Contracts
Gesuchte Skills: Design, Engineering
Projektbeschreibung
For our Life Sciences client in Switzerland, we care seeking for a Medical Device Senior Technical Expert.
Job title: Medical Device Senior Technical Expert - Testing
Start date: ASAP
End date: 30/06/2017
Location: Basel, Switzerland
YOUR ROLE:
- Analytical method development, validation and transfer.
- Define and document design verification testing, including transport verification testing.
- Laboratory activities, testing.
- Creating Design Control documentation and contributing to a high quality Design History file
- Monitor development and implementation of manufacturing processes
- Coordinate and monitor technical documentation
- Evaluating and challenging technical solutions
- Supporting medical device Risk management activities
- Supporting Human Factors Engineering activities
- Supporting and coordinating the manufacturing of clinical material and the production scale up
YOUR EXPERIENCE:
An ideal candidate would have a relevant degree in engineering and at least 7 years of experience in a similar area, including:
- Experience in analytical method development for design verification as well as for release testing
- Experience manufacturing process development and validation
- Mid-Early stage activities eg Design verification testing, design for manufacturing (prototype to model, manufacturing feasibility). Late stage activities eg tool qualification; equipment qualification;
- Manufacturing activities eg instruction process;
- DHF compilation
- Experience in testing needed for design verification as well as manufacturing validation
- Good technical knowledge of parenteral packaging and medical devices
- Development and documentation of drug/device combination products and medical devices, including Design Control process and other applicable regulatory, QA and GMP aspects
- Experience of managing external suppliers
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 Senior Technical Expert - Testing
Start date: ASAP
End date: 30/06/2017
Location: Basel, Switzerland
YOUR ROLE:
- Analytical method development, validation and transfer.
- Define and document design verification testing, including transport verification testing.
- Laboratory activities, testing.
- Creating Design Control documentation and contributing to a high quality Design History file
- Monitor development and implementation of manufacturing processes
- Coordinate and monitor technical documentation
- Evaluating and challenging technical solutions
- Supporting medical device Risk management activities
- Supporting Human Factors Engineering activities
- Supporting and coordinating the manufacturing of clinical material and the production scale up
YOUR EXPERIENCE:
An ideal candidate would have a relevant degree in engineering and at least 7 years of experience in a similar area, including:
- Experience in analytical method development for design verification as well as for release testing
- Experience manufacturing process development and validation
- Mid-Early stage activities eg Design verification testing, design for manufacturing (prototype to model, manufacturing feasibility). Late stage activities eg tool qualification; equipment qualification;
- Manufacturing activities eg instruction process;
- DHF compilation
- Experience in testing needed for design verification as well as manufacturing validation
- Good technical knowledge of parenteral packaging and medical devices
- Development and documentation of drug/device combination products and medical devices, including Design Control process and other applicable regulatory, QA and GMP aspects
- Experience of managing external suppliers
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