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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 responsibilitiesYou 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 ProfileYou 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

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Who we are

At Roche, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity.

Roche at Penzberg, near Munich, employs more than 7,000 people. The site is one of the largest biotechnology centers in Europe and the only Roche site with research, development and production for both Pharmaceuticals and Diagnostics under one roof. From your beginning with Roche, our motivated team will welcome and support you. Numerous opportunities for personal development, flexible work hours, attractive compensation packages and special family assistance programs are available.

Roche is an Equal Opportunity Employer.