Medical Device Project Leader

Basel  ‐ Vor Ort
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Beschreibung

Medical Device Project Leader wanted for our Basel based client in the pharmaceutical sector.

Your experience/skills:
  • University degree in Packaging Science/Engineering or Mechanical Engineering or University level Engineering education
  • 7 + years' work experience in leading device development technical teams or in a similar area along with profound background in Project and Program Management
  • Know-How of pharmaceutical development in general and Medical Device Regulations such as FDA 21CFR 820, FDA 21CFR Part 4, EU Medical Device Directive, EU Medical Device Regulation
  • Competency in developing and writing of technical documentation, in drug/device combination products and medical devices as well as in Design Control process and other applicable regulatory, QA and GMP aspects
  • Good command of managing external suppliers, Product Design or Design for Manufacture and of test and verification, including development of methods and equipment
  • General understanding of Human Factors Engineering, clinical studies processes, risk management and requirements
  • Languages: fluent English both written and spoken, German and French would be an advantage


Your tasks:
  • Conducting the definition of product requirements for packaging, delivery systems and medical devices such as drug and device combination products
  • Observing work progresses and supporting technical development including test and verification work as well as controlling the development and implementation of manufacturing processes
  • Supplying primary packaging and device expertise in a broader cross-functional drug product development team as well as managing the collaboration with external development partners
  • Supporting and coordinating the manufacturing of clinical material and the production scale up
  • Providing support to cross functional project teams in the development, review and submission of regulatory dossiers along with monitoring Human Factors Engineering activities
  • Managing and securing Risk management activities, design verification activities and technical documentations
  • Maintaining high quality of Design History File and transferring it to production


Start:
Duration: 06MM+
Location: Basel, Switzerland
Ref.Nr.: BH13522

Does this sound like an interesting and challenging opportunity to you? Then take the next step by sending us your CV as a Word document and a contact telephone number.

Due to work permit restrictions we can unfortunately only consider applications from EU or Swiss citizens as well as current work-permit holders for Switzerland.

Going the extra mile…
Start
10/2018
Dauer
6 months
Von
RM Group
Eingestellt
25.09.2018
Projekt-ID:
1638380
Vertragsart
Freiberuflich
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