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The Position
A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.
As a Biospecimen Senior Specialist (m/f/d), you are responsible for the acquisition of biospecimens (human biological material) and all related sample data, in compliance with local legal requirements and quality standards.

Your key responsibilities

• You plan and carry out the acquisition of routine and complex (bio)samples to meet the requirements of the project teams and functional areas in Research and Development.
• You work closely with internal and external stakeholders, including Global Procurement, the Legal Department, SHE, Quality, and others, to ensure all operational and regulatory requirements are met.
• You ensure that all processes and documentation comply with GxP principles and standards, and manage the associated sample data and documentation.
• You monitor the progress of sample acquisition projects, identify and resolve any discrepancies or deviations, and respond promptly and professionally to changing priorities.
• You leverage your scientific expertise and knowledge when collaborating with suppliers and internal stakeholders to ensure compliance with applicable laws, regulations, and ethical standards.
• You provide support and coaching for your colleagues and act as a role model in your function.

Your Profile

• You have completed your studies in a scientific discipline or a related field and bring several years of professional experience in areas such as research, pharmaceuticals, medical device industry, diagnostic laboratories, or Contract Research Organizations (CRO).
• You have experience in the procurement of biospecimens, biobanking, clinical studies, laboratory diagnostics, or related fields, as well as in a regulated environment.
• You are proficient in German and English at a business level and can communicate effectively both in writing and verbally.
• You have solid knowledge of MS Office and/or Google Suite, are familiar with GLP/GCP requirements, and are knowledgeable about LIMS or other validated data/document management systems.
• You communicate excellently and have the ability to effectively collaborate with internal stakeholders and cross functional interfaces to achieve desired results.
• You work solution-oriented, precisely, and with a high level of quality awareness. You can effectively set priorities and manage multiple projects simultaneously in a dynamic environment.

Your application
We make things easier for you: Please upload only your current and compelling CV and your certificate of your highest degree.
We look forward to receiving your application!

• You plan and carry out the acquisition of routine and complex (bio)samples to meet the requirements of the project teams and functional areas in Research and Development.
• You work closely with internal and external stakeholders, including Global Procurement, the Legal Department, SHE, Quality, and others, to ensure all operational and regulatory requirements are met.
• You ensure that all processes and documentation comply with GxP principles and standards, and manage the associated sample data and documentation.
• You monitor the progress of sample acquisition projects, identify and resolve any discrepancies or deviations, and respond promptly and professionally to changing priorities.
• You leverage your scientific expertise and knowledge when collaborating with suppliers and internal stakeholders to ensure compliance with applicable laws, regulations, and ethical standards.
• You provide support and coaching for your colleagues and act as a role model in your function