Principal Research Scientist I/II Biologics Quality Control in Biologics Analytical R&D (all genders) (full-time, permanent)
AbbVie
- Location
- Ludwigshafen, RP, Germany
- Employment
- Full Time
- Work model
- On-Site
- Level
- Principal
- H-1B history
- 94 approvals (FY2023)
- Posted
- 1h ago
Skills
About this role
Principal Research Scientist I/II Biologics Quality Control in Biologics Analytical R&D (all genders) (full-time, permanent) Vollzeit Workday Global Grade: 18 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 People. Passion. Possibilities. Three words that make a world of difference. More than a job. It's a chance to make a real difference. Welcome to AbbVie! As part of an international company with 58,000 employees worldwide and around 3,500 employees in Germany, you will have the opportunity of addressing some of tomorrows 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 of developing and increasing your own skills? Youve come to the right place! Together, we break through – as Principal Research Scientist I/II Biologics Quality Control in Biologics Analytical R&D (all genders) The Principal Scientist I/II will be an integral part of the Analytical Innovation and Mass Spectrometry Team in the Bio CMC division. The role involves supporting analytical aspects of biologics products with a focus on advancing AbbVie’s early-stage clinical programs. This position calls for an individual with a strong technical analytical background, demonstrated leadership skills and the ability to effectively communicate and work cross-functionally. Make your mark : Lead and mentor scientists specializing in separation-based assays including HPLC and capillary electrophoresis for sample testing to support biologics mab and DS process development, characterization, validation as well as GMP manufacturing investigation activities. Serve as analytical representative in AbbVie's CMC teams, supporting early-stage biologics pipeline assets. Balance stakeholder expectations to ensure effective collaboration. Serve as the subject matter expert for analytical test methods, providing expertise and support for method development, execution, and troubleshooting. Evaluate and select effective analytical technologies and methods to meet program needs. Support automation and development of high-throughput analytical methods and drive timely delivery of high-quality testing results. Participate in the preparation and review of technical documents for early-stage programs. Take responsibility for analytical test methods, their development and validation, test method transfer to internal and external partners, as well as perform batch release activities Collaborate with other analytical teams in R&D and PDS&T on program transition, workflow and program strategic alignment. Provide guidance to peers on project management, analytical strategy, and technical skills related to separation techniques. Communicate project data, issues and risks to relevant teams. Promote proactive risk resolution within and across functional areas to advance project objectives. Demonstrate scientific excellence, advance science and innovation. Implement novel analytical techniques to enhance method robustness and expand analytical capabilities. Qualifikationen This is how you make a difference: PhD in chemistry, biology, biochemistry, chemical engineering, or related technical discipline. Minimum of 8+ years (PhD) of professional experience working in biotech/pharmaceutical setting. Proven experience managing and leading analytical development and QC