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Scientist – Analytics, Technical Operations

Oslo, Norway

Pay
Salary not listed in the saved posting
Work setup
Unconfirmed
Employment
Temporary — employment source
This is an opportunity to combine hands-on scientific work with analytical problem-solving and cross-functional collaboration in a regulated biotechnology environment. Please note: This is a temporary position for a period of one year. Discover Impactful Work
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What you’ll work on

Full posting
  • You will collaborate closely with colleagues across R&D, Technical Operations, Quality, QC, and other functions.

From the employer’s posting
In this role, you will take analytical ownership in cross-functional product development and improvement projects, working from analytical method development and validation through technology transfer and implementation in Quality Control (QC). You will collaborate closely with colleagues across R&D, Technical Operations, Quality, QC, and other functions. This is an opportunity to combine hands-on scientific work with analytical problem-solving and cross-functional collaboration in a regulated biotechnology environment.

What you’ll bring

All qualifications

Core experience

  • Demonstrated experience with analysis and interpretation of complex experimental and analytical data, including the use of appropriate statistical tools and methods.
  • Knowledge of working in a regulated environment and relevant quality standards, such as ISO 13485 is an advantage.
  • Experience with technology or analytical method transfer is an advantage.
  • Experience supporting QC investigations, including OOS/OOT investigations, is an advantage.
  • Knowledge, Skills and Abilities:
  • Ability to work independently while collaborating effectively in cross-functional teams.
Qualification wording
Demonstrated experience with analysis and interpretation of complex experimental and analytical data, including the use of appropriate statistical tools and methods.
Knowledge of working in a regulated environment and relevant quality standards, such as ISO 13485 is an advantage.
Experience with technology or analytical method transfer is an advantage.
Experience supporting QC investigations, including OOS/OOT investigations, is an advantage.
Knowledge, Skills and Abilities:
Ability to work independently while collaborating effectively in cross-functional teams.

Benefits in the posting

Full benefits wording
  • We offer competitive benefits, including an annual incentive plan, healthcare benefits, and additional employee benefits.

From the employer’s posting.

Job description

View original posting ↗

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

We are looking for a motivated and experienced Scientist to join our Analytics team within Technical Operations!


In this role, you will take analytical ownership in cross-functional product development and improvement projects, working from analytical method development and validation through technology transfer and implementation in Quality Control (QC).


You will collaborate closely with colleagues across R&D, Technical Operations, Quality, QC, and other functions.


This is an opportunity to combine hands-on scientific work with analytical problem-solving and cross-functional collaboration in a regulated biotechnology environment.


Please note: This is a temporary position for a period of one year.



Discover Impactful Work


As part of the Analytics team, you will contribute to the development, validation, transfer, and continuous improvement of analytical methods supporting products for life science, diagnostics, and clinical markets.

You will have the opportunity to work with advanced biotechnology, solve complex analytical challenges, and contribute directly to product quality and successful product development.



A Day in the Life


In this role, you will:

  • Serve as the analytical lead in cross-functional new product development and improvement projects.
  • Develop and optimize analytical methods for product release, in-process controls, and incoming raw-material testing.
  • Design, execute, analyze, and document feasibility, stability, comparability, and validation studies.
  • Lead or support analytical method transfer between sites, departments, and QC.
  • Support implementation of new analytical methods in QC.
  • Drive continuous improvement of analytical methods, procedures, and QC processes.
  • Provide scientific support to QC, including troubleshooting and investigation of out-of-trend (OOT) and out-of-specification (OOS) results.
  • Analyze and interpret complex experimental data using appropriate statistical approaches.
  • Communicate scientific results, recommendations, and technical concepts effectively to both specialist and cross-functional audiences.
  • Collaborate across functions to plan and coordinate project activities.
  • Support investigations related to customer complaints, problem notifications, and corrective and preventive actions (CAPA).



Keys to Success


We are looking for someone who combines strong analytical and scientific capabilities with a structured, collaborative approach.


Education


  • MSc or higher in analytical chemistry, molecular biology, biotechnology, or a related scientific discipline.

The successful candidate is expected to have:


  • Several years of relevant professional experience in analytical method development, optimization, and validation within biotechnology, life sciences, diagnostics, pharmaceuticals, or a related field.
  • Several years of hands-on experience independently designing, planning, executing, and documenting complex scientific experiments.
  • Demonstrated experience with analysis and interpretation of complex experimental and analytical data, including the use of appropriate statistical tools and methods.
  • Knowledge of working in a regulated environment and relevant quality standards, such as ISO 13485 is an advantage.
  • Experience with technology or analytical method transfer is an advantage.
  • Experience supporting QC investigations, including OOS/OOT investigations, is an advantage.



Knowledge, Skills and Abilities:


  • Strong analytical and problem-solving skills.
  • A structured and quality-focused approach to scientific work.
  • Ability to work independently while collaborating effectively in cross-functional teams.
  • Strong communication and interpersonal skills.
  • Excellent written and spoken English, including technical and scientific writing.
  • Ability to read and understand Norwegian



What We Offer


You will join a collaborative scientific environment where you can develop your expertise across analytical development, product development, technology transfer, and Quality Control.


The role offers a varied combination of scientific problem-solving, hands-on analytical work, cross-functional collaboration, and continuous improvement within a regulated environment.


At Thermo Fisher Scientific, you will be part of an innovative, global organization with opportunities for professional development and the chance to contribute to work that has meaningful impact.


We offer competitive benefits, including an annual incentive plan, healthcare benefits, and additional employee benefits.


We review applications continuously and may progress with suitable candidates as they apply, so we encourage you to submit your application as soon as possible. We look forward to your application!

Your next step

  • Have your CV and examples of relevant work ready.
  • Check the listed location, eligibility and core experience before starting.
  • Ask the employer about the salary range before committing time to the process.

Complete your application on thermofisher.wd5.myworkdayjobs.com. The employer’s form will show what is required.

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Source & posting history

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Pay

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Location & working pattern

Oslo, Norway

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Status in our records
Active
First seen by us
Sep 28, 2026
Recorded sightings
17
Last seen by us
Oct 10, 2026
Employer says posted
Sep 25, 2026

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