LC-MS Analytical Technician – ADME Drug Development

Novo Nordisk

Denmark

On-site

DKK 438,000 - 643,000

Full time

6 days ago
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Benefits offered by this job

Pension scheme
Holiday allowance
Free choice account

Job summary

Novo Nordisk in the Copenhagen area is seeking a Laboratory Technician for Development ADME. You will generate analytical data to reveal ADME properties of drug candidates using LC-MS, supporting safety evaluations and regulatory submissions.

You will contribute to developing workflows, maintain LC-MS equipment, and work closely with scientists and technicians in a collaborative, open environment.

Qualifications

  • Education as a Laboratory Technician
  • Hands-on LC-MS experience
  • Biological matrices sample preparation experience
  • Ability to maintain and troubleshoot LC-MS instrumentation
  • Interest in digitalisation and automation of workflows
  • Good written and spoken English
  • Ability to work independently and collaboratively
  • Open, flexible and solution-oriented mindset
  • Balance hands-on lab work with technical problem-solving and teamwork
  • Experience in bioanalysis, drug metabolism or pharmaceutical development is valued

Responsibilities

  • Plan and conduct LC-MS‑based analyses of drug candidates in biological matrices
  • Perform sample preparation and support ADME studies
  • Process analytical data and interpret results with scientists
  • Operate, maintain and troubleshoot LC-MS instrumentation
  • Develop and optimise analytical workflows and documentation
  • Participate in digitalisation and automation initiatives

Skills

Liquid chromatography
Mass spectrometry
Biological sample preparation
Digital automation mindset
English communication

Education

Education as a Laboratory Technician

Tools

LC-MS instrumentation
Data processing software

Job description

Novo Nordisk in the Copenhagen area is seeking a Laboratory Technician for Development ADME. You will generate analytical data to reveal ADME properties of drug candidates using LC-MS, supporting safety evaluations and regulatory submissions.

You will contribute to developing workflows, maintain LC-MS equipment, and work closely with scientists and technicians in a collaborative, open environment.

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