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Salary3B Pharmaceuticals (3BP) is a leading developer of targeted molecular radiopharmaceuticals focusing on cancer indications with high medical need. The focus of our drug development programs is a theragnostic approach using diagnostic imaging to identify patients who are likely responders to radiopharmaceutical therapy. 3BP has built a unique technology platform for the efficient discovery and validation of cancer radiopharmaceuticals. We are currently expanding our discovery and CMC activities and are looking for a Radioanalytical Specialist (m, f, d) to support these. Radioanalytical Specialist (m/f/d) The Radioanalytical Specialist (RS) will be part of the interdisciplinary Radiopharmaceutical Technologies team and work in close collaboration with 3BP's analytical as well as translational and clinical CMC experts, and interact with the Quality Assurance team. The RS will develop, qualify and validate quality control methods for our clinical development candidate compounds in order to support the Tech Transfer to and troubleshooting activities at third party labs. While this position is mainly lab-based, this includes also drafting appropriate technical documentation and potential travel. Furthermore, the RS will support our discovery activities by developing, implementing and executing routine as well as sophisticated analytical assays for the characterization of our discovery compounds. Part of the activities of the RS will be also instrument qualification and maintenance as well as the performance of radiolabelings using established protocols. In order to fulfil this role, the RS shall be confident in communicating with multiple internal and external stakeholders and able to deal with different perspectives on requirements and priorities. The candidate will be able to inspire others and have a collaborative and open-minded style that fosters a supportive working environment for the team. Mentorship and support will be available, although the candidate should thrive with minimal direct supervision and should have a strong creative drive. A high degree of initiative, accountability and control over their own day-to-day activities is required. Key Responsibilities Development, qualification and validation of quality control methods with focus on radio-HPLC Instrument qualification, troubleshooting and maintenance Radiolabelings using established protocols Drafting of technical documentation Tech transfer support Communication with internal and external stakeholders and partners Extensive analytical method development experience with focus on HPLC including writing, developing and working under appropriate technical documentation Experience in development of other standard quality control methods for radiopharmaceuticals (e.g., radio-TLC) and performance of radiolabelings is a plus Proficiency in effectively troubleshooting operational, application and other instrument problems is highly desired Knowledge of CMC and radiation safety protection regulatory requirements is beneficial Strong interest in interdisciplinary team work Ability and willingness to establish and build internal relationships at all levels Experience in communication with internal and external collaborators Proficient written and spoken English communication skills, German skills are highly desired Bachelor/Master Degree in a relevant field, e.g. (analytical ) chemistry Right to live and work in Germany An open and appreciative corporate culture with a strong team spirit Attractive employment conditions in a growing company with flat hierarchies You work independently and self-responsible Permanent employment, flexible working time model (full time is preferred but part time negotiable) Potential to develop your role as the company grows or requirements appear
