LC-MS Lab Technician for ADME & Drug Development

Novo Nordisk A/S; Måløv; On-site; DKK 438,000 - 643,000; Full time

Benefits offered by this job

Pension scheme

Free choice account

Holiday allowance

Job summary

Novo Nordisk A/S in Denmark is seeking a Laboratory Technician with LC-MS Capabilities to support Development ADME. You will generate high-quality analytical data to study drug absorption, distribution, metabolism, and excretion using LC-MS across biological matrices, helping advance drug candidates.

Join a scientifically diverse team of 10 professionals and contribute to developing workflows, maintaining instrumentation, and producing robust documentation for regulatory submissions.

Qualifications

• Education as a Laboratory Technician.
• Hands-on LC-MS experience and sample prep.
• Proactive, independent worker with good English.

Responsibilities

• Plan and conduct LC-MS analyses of drug candidates in biological matrices.
• Perform sample preparation and support a broad range of Development ADME studies.
• Process analytical data and contribute to interpreting results together with scientists.
• Operate, maintain and troubleshoot LC-MS instrumentation and other laboratory equipment.
• Contribute to developing and optimising analytical workflows and laboratory processes, and ensure high-quality experimental documentation.
• Participate in or drive local digitalisation and automation initiatives.

Skills

LC-MS experience

Sample preparation

Instrument maintenance

Lab automation

English proficiency

Independent work

Education

Laboratory Technician education

Tools

LC-MS software

Job description

Novo Nordisk A/S in Denmark is seeking a Laboratory Technician with LC-MS Capabilities to support Development ADME. You will generate high-quality analytical data to study drug absorption, distribution, metabolism, and excretion using LC-MS across biological matrices, helping advance drug candidates.

Join a scientifically diverse team of 10 professionals and contribute to developing workflows, maintaining instrumentation, and producing robust documentation for regulatory submissions.