Subject Matter Expert – Analytical Operations & Process Optimization (CDMO)Location:Europe (Multi-site travel required – up to 70%)Industry:Contract Development and Manufacturing Organization (CDMO) – Pharmaceuticals / BiotechPosition OverviewWe are seeking an experienced and driven Subject Matter Expert (SME) in large-scale analytical testing to join a high-impact team supporting a leading CDMO client across multiple European sites. This role is ideal for a professional with deep expertise in operational efficiency, analytical process improvement, and troubleshooting complex laboratory operations, who thrives in a dynamic, multi-site environment.As a trusted advisor to the client’s operations, you will play a pivotal role in scaling up, standardizing, and optimizing analytical processes in line with global best practices. Your contributions will directly support commercial and late-stage development programs.Key ResponsibilitiesAct as a technical lead and subject matter expert for analytical laboratory operations across multiple CDMO sites in Europe.Identify and implement operational efficiencies, including automation opportunities, data workflows, and right-first-time improvements.Drive harmonization and standardization of processes and documentation across labs.Support analytical method optimization, troubleshooting, and tech transfer initiatives.Collaborate with Quality, Production, and R&D teams to ensure GMP compliance and regulatory readiness.Deliver training, workshops, and mentoring to site teams on best practices in analytical operations and continuous improvement (CI).Analyze KPIs and operational data to identify trends, root causes, and performance gaps.Champion the adoption of LEAN, 5S, and OPEX methodologies to increase lab productivity and reduce variability.Ideal Candidate ProfileDegree in Chemistry, Pharmaceutical Sciences, or related scientific discipline.8+ years of experience in analytical laboratories within pharmaceutical or biotech environments, ideally in a CDMO setting.Proven track record of process improvement, troubleshooting, and analytical scale-up.In-depth knowledge of GMP, ICH guidelines, and analytical instrumentation (e.g., HPLC, GC, Empower).Experience implementing LEAN/OPEX/5S principles in laboratory settings.Strong communication and interpersonal skills, with ability to influence cross-functional teams and engage at all organizational levels.Willingness to travel extensively across Europe (up to 70%).What We OfferStrategic and impactful role with high visibilityExposure to cutting-edge pharmaceutical and biotech projectsOpportunity to work across diverse European operationsCompetitive compensation and travel packageCollaborative, innovation-driven culture