Job Description:
A Clinical Laboratory Scientist in Zurich is vital in delivering accurate diagnostic results by performing routine and specialized lab tests on biological samples. The role requires working with clinical instruments for hematology, biochemistry, immunology, and microbiology assays. Scientists ensure proper specimen processing, calibration of instruments, and adherence to quality control procedures. In Zurich’s hospital or private diagnostic settings, this role is central to patient care decisions. They also support clinical trials and research studies by processing trial samples and analyzing clinical endpoints. Strict compliance with health, safety, and ISO or CAP accreditation standards is required. Documentation, data reporting, and regular liaison with clinicians or medical staff form part of the role. Precision, responsibility, and ethical conduct are vital.
Job Requirement:
Bachelor’s, Master’s, or Ph.D. in Biotechnology, Molecular Biology, Life Sciences, Biochemistry, or a related field.
Strong understanding of biological systems, scientific methodologies, and lab safety protocols.
Demonstrated experience in laboratory research, scientific data analysis, and technical reporting.
Proficiency in using laboratory equipment, software tools for data interpretation, and bioinformatics platforms.
Familiarity with GMP, GLP, GCP, and other regulatory compliance standards applicable to clinical and laboratory environments.
Strong documentation and record-keeping skills in accordance with industry standards.
Ability to design, execute, and troubleshoot experiments and assays independently or in a team.
Excellent written and verbal communication skills for preparing research documentation and collaborating across departments.
Detail-oriented with strong analytical thinking, problem-solving, and organizational capabilities.
Adaptability to fast-paced, collaborative, and evolving research and clinical settings.
Understanding of ethical research practices and commitment to maintaining data integrity and confidentiality.
Previous experience with clinical trials, product development, or regulatory processes is considered an advantage.
Ability to work with cross-functional teams including R&D, Quality, Regulatory, and Manufacturing.
Good time management skills and ability to meet tight project deadlines.
Fluency in English is mandatory; knowledge of German or French is a plus for Swiss workplaces.
Willingness to undergo ongoing training and certification as required by the organization.
