Arbeitgeber: Celonic Deutschland GmbH & Co. KG

THE COMPANY
Celonic 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-purpose
Provide scientific and technical expertise in analytical methods, technologies, and experimental strategies, supporting complex analytical challenges by problem-solving and decision-making
Ensure 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 documents
Identify risks and proactively drive solutions related to analytical performance, deviations, documentation, timelines, and other operational challenges
Lead the implementation and transfer of analytical technologies across Celonic sites and functions, ensuring effective knowledge transfer and successful technical implementation
Collaborate across functions, working closely with project teams, SMEs, support functions, external partners, and client-facing teams to align analytical activities with project and business priorities
Share expertise and develop technical capability by coaching and training colleagues, supporting knowledge sharing, and continuously developing expertise in emerging analytical technologies and approaches
Promote a culture of continuous improvement, innovation, safety, and compliance within Analytical Services

MSc, PhD, or equivalent degree in Biology, Biotechnology, Chemistry, Chemical Engineering, or a related scientific discipline
8+ years of relevant experience in pharmaceutical, biotechnology, CDMO, or a comparable analytical environment
Strong practical experience in analytical development, method optimization, transfer, validation, and cGMP-regulated activities
Strong 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 expectations
Proven ability to lead complex analytical activities, solve challenging analytical problems, and coordinate work across functions and organizational boundaries
Strong experience with analytical documentation and data evaluation, combined with a hi...