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QA/QC Expert
Eingestellt von Experis AG
Gesuchte Skills: Support, Client
Projektbeschreibung
QA/QC EXPERT - BASEL - 100%
Experis is the global leader in professional resourcing and project-based workforce solutions. Our suite of services range from interim and permanent recruitment to managed services and consulting, enabling businesses to achieve their goals. We accelerate organisational growth by attracting, assessing and placing specialised professional talent.
For our international client based in Basel, Experis is currently looking for a QA/QC Expert for a contracting position until end of 2018.
General information:
Start date: ASAP
End date: 31.12.2018
Work location: OnSite in Basel
Workload: 100%
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.
* Support project management functions as a sub-team member in preparation for a Pre-Approval Inspection.
* Write/contribute to internal compliance policy and/or comment to regulations.
* Lead and support direct reports in line with our values and behaviour including objectives setting, performance evaluations, development planning and participate in recruiting process.
You bring for this role the following qualifications:
Education: Graduate in Chemistry, Pharmacy, Microbiology or Biotechnology or another related science
Languages: English fluent in speaking/writing, German and/or French desirable
Experience:
* At least 3 years of relevant experience.
* Ability to influence people, negotiate and communicate.
* Sound scientific, technical and regulatory knowledge in a specific area.
* Excellent knowledge of cGMP, working knowledge of medical device and combination product regulations, standards and guidelines.
* Good knowledge of medical device development and life cycle management.
* Good organizational skills.
* Good and proven ability to analyse and evaluate GMP compliance.
Interested in this opportunity?
Kindly send us your CV today through the link in the advert. However should you have any questions please contact Stéphanie Vogt.
Experis is the global leader in professional resourcing and project-based workforce solutions. Our suite of services range from interim and permanent recruitment to managed services and consulting, enabling businesses to achieve their goals. We accelerate organisational growth by attracting, assessing and placing specialised professional talent.
For our international client based in Basel, Experis is currently looking for a QA/QC Expert for a contracting position until end of 2018.
General information:
Start date: ASAP
End date: 31.12.2018
Work location: OnSite in Basel
Workload: 100%
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.
* Support project management functions as a sub-team member in preparation for a Pre-Approval Inspection.
* Write/contribute to internal compliance policy and/or comment to regulations.
* Lead and support direct reports in line with our values and behaviour including objectives setting, performance evaluations, development planning and participate in recruiting process.
You bring for this role the following qualifications:
Education: Graduate in Chemistry, Pharmacy, Microbiology or Biotechnology or another related science
Languages: English fluent in speaking/writing, German and/or French desirable
Experience:
* At least 3 years of relevant experience.
* Ability to influence people, negotiate and communicate.
* Sound scientific, technical and regulatory knowledge in a specific area.
* Excellent knowledge of cGMP, working knowledge of medical device and combination product regulations, standards and guidelines.
* Good knowledge of medical device development and life cycle management.
* Good organizational skills.
* Good and proven ability to analyse and evaluate GMP compliance.
Interested in this opportunity?
Kindly send us your CV today through the link in the advert. However should you have any questions please contact Stéphanie Vogt.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Sonstiges