Scientist (m/f/d) for the area LC/MS (full-time)

Kymos Group; Frankfurt; Vor Ort; EUR 50.000 - 70.000; Vollzeit

Zusammenfassung

A leading Contract Research Organization is seeking an LC-MS Scientist in Frankfurt, Germany. The role involves developing and validating LC-MS/MS methods, conducting bioanalytical studies, and ensuring compliance with GLP standards. Ideal candidates will have a relevant degree and hands-on experience with LC-MS/MS systems. You will be part of a dynamic team focused on innovative drug development. This position offers stability, competitive salary, and opportunities for career growth.

Leistungen

Competitive salary and benefits package

Flexible working hours

Modern laboratory infrastructure

Training and mentoring

Company medical care

Qualifikationen

• Degree in a relevant field (B.Sc., M.Sc., or Diploma).
• Hands-on experience with LC-MS/MS systems.
• Understanding of GLP or similar regulated environments.

Aufgaben

• Develop and validate LC-MS/MS methods.
• Perform sample preparation and instrumental analysis.
• Execute study sample analysis in compliance with GLP.

Kenntnisse

Hands-on experience with LC-MS/MS systems

Fluent in German

Fluent in English

Analytical thinking

Problem-solving skills

Attention to detail

Ausbildung

Degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field

Tools

Sciex instruments

Jobbeschreibung

Location & Employment

• Location: Frankfurt am Main (Germany)
• Contract: Permanent
• Working day: Full time
• Sector: Pharmaceutical and biopharmaceutical
• Vacancies: 1
• Discipline: R&D
• Work modality: On site

Company Overview

Kymos Group is a medium‑size, fast‑growing Contract Research Organization (CRO) with headquarters in Spain and laboratories in Spain, Italy, and Germany, plus a liaison office in South Korea. We offer comprehensive bioanalytical and CMC analytical services to the life sciences industry. Our GMP‑ and GLP‑certified laboratories are GCP compliant and have been inspected by EMA, FDA, and ANVISA.

Kymos is devoted to delivering high‑quality, value‑added services and is highly oriented toward innovation. We provide research, development, and quality‑control services across small molecules, proteins, antibodies, nucleic acids, and advanced therapies.

With more than 200 employees, we promote diversity, gender equality, well‑being, and initiative, encouraging career development and internal promotion.

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 develop and validate LC‑MS/MS methods according to ICH M10 guidelines and perform study sample analysis under GLP. Your work involves diverse projects from preclinical and exploratory studies to Phase I‑III clinical trials and bioequivalence studies. Working closely with laboratory scientists, study directors, and quality assurance, you will ensure scientific rigor, regulatory compliance, and timely project delivery.

Your Key Responsibilities

• Develop, optimise, and validate LC‑MS/MS methods for small molecules 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 write reports.
• Troubleshoot analytical methods and instrumentation.
• Take responsibility for a whole project with the possibility to become study director in the future.
• Act as 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.

Requirements

• 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.