Job Description:
An Applied Biosciences Specialist in Geneva is involved in translating biological research into real-world applications such as diagnostics, therapeutics, agriculture, or environmental sustainability. The role includes conducting experiments, optimizing protocols, and developing biological products or tools. Specialists work in a multidisciplinary environment to apply genetic, molecular, and cellular technologies to solve practical problems. Responsibilities include analyzing large datasets, validating methods, and working with bioinformatics tools to draw actionable insights. The specialist plays a vital role in product development, from prototype evaluation to performance testing. In Geneva’s dynamic life sciences sector, the role also includes working with regulatory teams to ensure compliance with international standards. Coordination with clinical and commercial units may be required during late-stage development or deployment phases. The position requires staying up to date with current scientific literature and contributing to patent filings or scientific communication. Adaptability and strong cross-functional collaboration are essential.
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.
