Postdoctoral researcher in Regulatory Science related to biotechnology/biomedical products (f/m/d)

Postdoctoral researcher in Regulatory Science related to biotechnology / biomedical products (f/m/d)

A focus of our research are Engineered Living Materials (ELMs), an emergent class of materials at the interface between materials science and synthetic biology, with huge potential for sustainable innovation in different technological and medical fields. Our institute develops safe‑by‑design concepts for responsible ELM innovation.

To lead a community‑driven initiative in ELMs, we seek a postdoctoral researcher to perform research on needs, challenges and expectations for the development of safe and sustainable ELM‑based technologies, and to elaborate guidelines for researchers and developers of ELMs. The scientist will coordinate and work together with a network of experts from relevant stakeholders with interest in ELM research, innovation and regulation (academic institutions, industry, consultants, regulatory agencies). This project is framed within the collaborative network MaterialVital Hub, recently funded by the Federal Ministry of Research, Technology and Space (BMFTR).

Your roles

• Analysis of needs, challenges and upcoming expectations for ELM regulation through interviews and dedicated workshops with experts.
• Systematic analysis and documentation of existing frameworks of relevance for ELM regulation.
• Expansion of an existing network of experts. Communication and coordination of the work within the network.
• Conceptualization and implementation of information exchange and documentation formats within the network.
• Elaboration of praxis‑oriented guidelines, decision‑making trees and proposing metrics for safe‑by‑design approaches in ELM research that help integrating safety aspects at early stage of materials design, informed by the exchange among experts in the network.
• Conceptualization of the outreach action plan (website, online platform, workshops) in cooperation with scientists in MaterialVital Hub and communication experts at INM and partner institutions.
• Reporting to project coordinator, partners and funding agencies.

Your profile

• PhD in Regulatory Affairs related to biotechnological or pharmaceutical topics. Alternatively, university degree in natural, engineering or life sciences and previous experience in regulatory affairs at the industry or regulatory agencies. Alternatively, a PhD in biomedical materials, pharmaceutical science or microbiology, with experience in clinical translation of cell therapies.
• Interest in inter- and transdisciplinary challenges.
• Strong analytical skills.
• Proactive, problem‑solving, structured and autonomous working style.
• Writing and communication skills in German and English.

We offer

• An interesting and timely topic with high visibility and opportunities for interaction with public and private partners.
• A network of interested partners to collaborate with you and support your work.
• A dynamic environment with substantial room for creativity, profile and career development.
• A professional and supportive working environment with an open and international culture.
• A well structured on‑boarding process and clear responsibilities.
• Possibilities for further training and qualification.
• Flexible working hours and mobile working opportunity.
• A family‑friendly working place.
• A EG 13 TV‑L position (full time), initially for 3 years. A part time position is also possible.

Equal Opportunity Statement

The institute is an equal opportunity employer with a certified family‑friendly policy. We promote professional opportunities for women and encourage them to apply. People with disabilities are expressly encouraged to apply and will be given priority if equally qualified.