Post-Doc – Innovative manufacturing concepts on Biologics (all genders) (full-time, temporary for 24 months)

Post-Doc – Innovative manufacturing concepts on Biologics (all genders) (full-time, temporary for 24 months) Vollzeit Workday Global Grade: 12 Unternehmensbeschreibung About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Stellenbeschreibung The job that makes possibilities real in patients' lives. And yours. The job that helps you get ahead in life. Moving mountains together. Welcome to AbbVie! As part of an international company with 48,000 employees worldwide and around 3,000 employees in Germany, you will have the opportunity of addressing some of tomorrow’s unmet medical needs in close collaboration with your colleagues. Are you passionate about improving global health care? Do you want to contribute to improving patients' quality of life through your expertise? In a challenging work environment that offers opportunities for developing and increasing your own skills? You’ve come to the right place! Moving mountains together – as Post-Doc – Innovative manufacturing concepts on Biologics (all genders) Early Manufacturing Process Development (EMPD) within Biologics Drug Product Development is responsible for developing robust manufacturing processes for AbbVie's parenteral pipeline projects, supporting the advancement of biologics through early clinical stages. Biologics are often co-administered with other biologics to boost their clinical efficacy and the overall patient experience, while requiring multiple injections. Formulating both active ingredients into a single drug product significantly strengthens patient compliance and dose accuracy. This goes along with additional technical challenges for drug development and manufacturing, which will become your primary topics of interest through the upcoming 24 months. You will design, execute and assess studies to identify key risks and their mechanisms for co-formulating biologics during drug product development and manufacturing, comprising identified unit operations as well as in-process controls to enable a state-of-the-art, compliant and robust control strategy while maintaining maximum dose-range flexibility. Responsibilities Plan and perform systematic studies to dive deeper into innovative formulation concepts for biologic drug products Publish results in peer-reviewed journals and present work at internal panels and scientific conferences aligned with business objectives Collaborate with international multidisciplinary teams to advance project goals Participate in investigations on root cause analyses of development projects related to the scientific area Demonstrate a high degree of responsibility in maintaining scientific standards, and safe laboratory practices Maintain a high level of productivity in the laboratory setting Actively engage with scientific literature and apply insights to individual project(s) as well as the overall program Qualifikationen Ph.D. in pharmaceutical technology, biochemistry or related area, preferably with a background in parenteral/biological processing or similar. Work experience in the field of protein aggregation is advantageous Knowledgeable in aseptic handling techniques Experience with analytical methods to detect protein denaturation and aggregation as well as to detect/characterize particles in solution is advantageous Affinity for working hands-on with complex equipment and solve related technical problems Proficiency in spoken and written English German language skills are advantageous Record of scientific initiative and creativity in research or