(Poistunut julkaisusta)

Laboratory Scientist/Engineer in manufacturing QC
Thermo Fisher Scientific Oy

Alkuperäinen julkaisupäivä 23.1.2018

Laboratory Scientist/Engineer in manufacturing QC
Vantaa, Finland

We are now seeking Laboratory Scientist/Engineer in manufacturing QC to join our Operations organization for CDS business IVD analyzer manufacturing engineering team in Vantaa, Finland for 1 year temporary position.

You will be working in an exciting global company to introduce a new instrument and to develop our Vantaa Operations as a center of excellence for IVD instruments.

We are looking for an experienced LC/MS/QC person with strong hands-on problem-solving and communication capabilities with background in analytical chemistry, biomedical laboratory science or relevant field. You will be working in an exciting global company to introduce a new instrument and to develop our Vantaa Operations as a center of excellence for IVD instruments.

We are expecting active, work oriented team player who works independently but also comfortably navigates between R&D engineering, QARA, sourcing and manufacturing organizations. Our international working environment, fast paced working rhythm and sometimes rapidly changing operational environment require flexibility and continuous learning.


Key responsibilities:

  • Support and maintain IVD instrument production QC testing and MS incoming inspection processes
  • Maintain/update QC and MS testers and test SW (instructions, tools and MES)
  • Execute process validations and documentations
  • Update the manufacturing process risk assessment related to changes made to processes and testers.
  • Responsible for engineering change proposals (ECR) and implement engineering change orders (ECO) related to QC and MS working instructions and BOM changes (Agile and MES).
  • Participate manufacturing testing capability scaling up
  • Non-conformance handling process
  • Failure root-cause analysis, corrective action planning, and implementation


Experience / Qualification:

  • Two to four years of work experience in LCMS area (incl SWs and methods) (Analytical chemistry education, Biotechnology, chemistry or laboratory science education)
  • Experience in implementing and maintaining QC processes and tools
  • Experience in documenting and reporting
  • Good communication skills in spoken and written Finnish and English

Additionally we value:

  • Knowledge of FDA/In Vitro regulated diagnostic products manufacturing and related authority requirements
  • Experience in use of PLM and/or ERP system


We look forward to receiving your application, including a cover letter and CV and a salary request in English. Please apply via http://jobs.thermofisher.com/. Reference: 60892BR

Please apply by 18th of March, 2018.

Should you have any questions, please contact Process Engineering Manager Nina Björkman-Rintala at +358 50 3815506 on Tuesday the 6th of March between 14-16.

At Thermo Fisher Scientific, each one of our 65,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission - enabling our customers to make the world healthier, cleaner and safer.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.