German Speaking-Jobs in Deutschland

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

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.

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.

• 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.

• 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.

• 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.