Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
Quality Expert for Medical Mobile Applications
Eingestellt von Harvey Nash IT Recruitment Switzerland
Gesuchte Skills: Support, Client
Projektbeschreibung
For our client in BASEL (SWITZERLAND) we are looking for a QUALITY EXPERT FOR MEDICAL MOBILE APPLICATIONS for a 1 YEAR contract.
LOCATION: Basel
DURATION: 07/01/2019 - 31/12/2019
WORKLOAD: 100%
Background:
The Quality Expert has to ensure technical development and manufacturing operations of assigned Medical Devices/Combination Products are conducted in accordance with Quality System requirements, ensuring high product quality, regulatory compliance and operational efficiency.
Tasksparticipate in recruitment of talent. Support a culture of high performance and trust. Assure that the required level of knowledge and skills is available and identify competency gaps. Establish and implement training and development plans.
. Meet internal and external guidelines regarding quality and safety (quality manuals, regulatory cGMP guidelines, health authority requirements, SOPs, HSE, etc.). Promote and enforce compliance to guidelines. If managing associates, ensure same for them.
Requirements:
. At least 3 years of relevant experience
. Practical experience in IEC 62304, IEC 82304, ISO 14971, MDD/MDR, GDPR, 21 CFR part 820/part 4 requirements and in Medical Mobile Applications.
. Excellent knowledge of cGMP, working knowledge of medical device and combination product regulations, standards and guidelines.
. Graduate in Chemistry, Pharmacy, Microbiology or Biotechnology or another related science
. Good knowledge of medical device development and life cycle management.
. Fluent English. German and French is an asset
For further details please contact Mateusz Czarnocki.
LOCATION: Basel
DURATION: 07/01/2019 - 31/12/2019
WORKLOAD: 100%
Background:
The Quality Expert has to ensure technical development and manufacturing operations of assigned Medical Devices/Combination Products are conducted in accordance with Quality System requirements, ensuring high product quality, regulatory compliance and operational efficiency.
Tasksparticipate in recruitment of talent. Support a culture of high performance and trust. Assure that the required level of knowledge and skills is available and identify competency gaps. Establish and implement training and development plans.
. Meet internal and external guidelines regarding quality and safety (quality manuals, regulatory cGMP guidelines, health authority requirements, SOPs, HSE, etc.). Promote and enforce compliance to guidelines. If managing associates, ensure same for them.
Requirements:
. At least 3 years of relevant experience
. Practical experience in IEC 62304, IEC 82304, ISO 14971, MDD/MDR, GDPR, 21 CFR part 820/part 4 requirements and in Medical Mobile Applications.
. Excellent knowledge of cGMP, working knowledge of medical device and combination product regulations, standards and guidelines.
. Graduate in Chemistry, Pharmacy, Microbiology or Biotechnology or another related science
. Good knowledge of medical device development and life cycle management.
. Fluent English. German and French is an asset
For further details please contact Mateusz Czarnocki.
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
IT Entwicklung, Sonstiges