Job Description

As an

LC-MS Scientist

, you will play a key role in generating high-quality bioanalytical data that supports our clients' drug development programs. You will be responsible for developing and validating LC-MS/MS methods according to ICH M10 guidelines as well as performing study sample analysis under GLP. You will work on diverse projects ranging from preclinical and exploratory studies to Phase I-III clinical trials and bioequivalence studies. Working closely with other laboratory scientists, study directors, and quality assurance, you will ensure scientific rigor, regulatory compliance, and timely project delivery.



Your

key responsibilities

will be:


Develop, optimize, and validate LC-MS/MS methods for small molecule and/or biomolecules in biological matrices Plan and perform sample preparation, instrumental analysis, data processing, and data evaluation Execute study sample analysis in compliance with GLP and internal SOPs Document experimental work and results in accordance with regulatory standards and writing reports Troubleshoot analytical methods and instrumentation Responsibilityfor a whole project with the possibility to become study director in the future Interface between the laboratory and the customer (project management) Contribute to continuous improvement initiatives and technology development within the LC-MS laboratory

What We Offer

A dynamic, supportive team with flat hierarchies and a positive, inclusive culture Opportunity to work on innovative drug development programs for international biotech and pharma clients Stability and career development opportunities within a multi-international group Modern laboratory infrastructure with advanced LC-MS technology Training, mentoring, and ongoing professional development Competitive salary and benefits package Flexible Working hours / flextime Good accessibility by car and public transportation Free drinks (coffee, tea, water) Company medical care

Your Profile

Degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field (B.Sc., M.Sc., or Diploma) Hands-on experience with LC-MS/MS systems (ideally Sciex instruments) Experience in quantitative bioanalysis - Experience is a plus, but not required. Understanding of GLP or similar regulated environments is an advantage Strong analytical thinking, problem-solving skills, and attention to detail Ability to work independently as well as in a collaborative, fast-paced team * Fluent speaking, reading and writing in German and English