About this role
THE COMPANYCelonic is a “Pure Play” Biologics Contract Development Manufacturing Organization (CDMO). Celonic’s mission is to help its customers, primarily small to large Biotech Companies, bring life- saving and improving drugs effectively to the market using innovative, “next generation” bioprocessing technologies. Celonic has a state-of-the-art Biologics Development and Innovation Center in Basel, Switzerland (headquarters), and clinical and commercial GMP manufacturing facilities in Heidelberg, Germany. At present, more than 500 highly qualified employees work at Celonic's. Due to the expansion of the company, Celonic is looking for committed and qualified employees. As Analytical Lead QC - Protein Analytics / Chemical Analytics (f/m/d), you will take ownership of analytical activities within your assigned area, ensuring high scientific standards, quality, and on-time delivery. You will lead and coordinate analytical activities across optimization, transfer, validation, and troubleshooting, providing scientific and technical expertise to ensure robust, fit-for-purpose analytical solutions in line with cGMP and analytical lifecycle requirements. Acting with a high degree of autonomy, you will serve as a key interface between QC-Chemical Analytics, project teams, client-facing functions, and external partners. You will also contribute to the implementation and transfer of innovative analytical technologies across Celonic sites, supporting knowledge sharing and technical excellence.You will report directly to the Team Manager QC Chemical Analytics and operate as a technical leader without direct people-management responsibility.YOUR RESPONSIBILITIES:Lead analytical activities including optimization, transfer, validation, and troubleshooting, ensuring methods are scientifically sound and fit-for-purposeProvide scientific and technical expertise in analytical methods, technologies, and experimental strategies, supporting complex analytical challenges by problem-solving and decision-makingEnsure cGMP compliance, data integrity, and scientific rigor across analytical activities, documentation, data evaluation, and reporting, including the preparation and review of protocols, SOPs, reports, and other technical documentsIdentify risks and proactively drive solutions related to analytical performance, deviations, documentation, timelines, and other operational challengesLead the implementation and transfer of analytical technologies across Celonic sites and functions, ensuring effective knowledge transfer and successful technical implementationCollaborate across functions, working closely with project teams, SMEs, support functions, external partners, and client-facing teams to align analytical activities with project and business prioritiesShare expertise and develop technical capability by coaching and training colleagues, supporting knowledge sharing, and continuously developing expertise in emerging analytical technologies and approachesPromote a culture of continuous improvement, innovation, safety, and compliance within Analytical ServicesMSc, PhD, or equivalent degree in Biology, Biotechnology, Chemistry, Chemical Engineering, or a related scientific discipline8+ years of relevant experience in pharmaceutical, biotechnology, CDMO, or a comparable analytical environmentStrong practical experience in analytical development, method optimization, transfer, validation, and cGMP-regulated activitiesStrong practical experience in analytical methodology ( HPLC (RP, SEC, AEX), CE, Photo-spectrometry, PAGE, IEF)Strong knowledge of analytical method lifecycle, validation principles, European Pharmacopoeia, ICH guidelines, and CMC / regulatory expectationsProven ability to lead complex analytical activities, solve challenging analytical problems, and coordinate work across functions and organizational boundariesStrong experience with analytical documentation and data evaluation, combined with a hi...