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Job ID :
49984BR
Location :
Norway - Lillestrom|Norway - Oslo
:
Job Description
Quality Specialist
Lillestrøm & Oslo , Norway

Do you want to be part of our journey into the future? We produce products which are used in break-through technologies, lifesaving assays and clinical applications that demands high attention to quality assurance in all steps of the production and control processes. Our customers are world leading pharma and diagnostics companies which have chosen us as their business partner. This means that we as a company must continue to develop and improve our quality assurance systems on an elite level.

We are now looking for the right person to join our QA team. You will be working at both our sites and report to David Gillooly. This is a permanent position.

Key Responsibilities:
  • Drive activities within a cross-functional organization to ensure compliance of the company’s Quality Management System with ISO 13485:2016, ISO 9001:2015, with regulatory and customer requirements, and with company policies
  • Maintain controlled documents through the electronic Documentation Management System
  • Review production processes and quality tests to ensure that they are being conducted according to approved protocols and set specifications.
  • Coordinate the change control process through processing change control requests by reviewing accuracy, completeness & compliance with SOPs
  • Manage the electronic Document Management System by working as a Document Change Analyst
  • Coordinate and provide quality training
Who we are looking for:
  • You are systematic and organized
  • You have a strong desire for continuous improvement
  • Your work is of high quality and you transfer your standards and expectation of quality to your colleagues
  • You motivate and communicate well with everyone and at all levels in-house
  • You thrive on influencing others and are results driven
  • You enjoy working independently as well as in team settings
Experience/Qualifications needed to succeed:
  • Bachelors degree
  • Fluent (spoken and written) in a Scandinavian language as well as English
  • Experience from working with electronic databases, documentation handling
  • Experience from Medical Device or Pharmaceutical Industry is an advantage

If you would like to know more about the position - please contact Victoria Hicks Mørkved or David Gillooly.

We look forward to receiving your application. Please submit your motivation letter and CV through https://internaljobs.thermofisher.com/. Application deadline June 25, 2017.


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