Join a cutting-edge environment where your expertise will directly impact the development of innovative analytical methods in the pharmaceutical industry. Our client is on a mission to enhance method performance across multiple QC sites, and they are looking for a driven professional to help achieve this goal.

As a qualified candidate, you will be a dedicated Analytical Method Remediation SME passionate about ensuring robust analytical performance through strategic actions and collaborative approaches. This role is designed for someone who thrives in dynamic settings and is determined to lead initiatives that drive significant improvements.

• You drive CMV in-use execution across QC sites to ensure consistent detection and interpretation of method performance issues.
• You establish and maintain a clear operational linkage between CMV outputs and AMR intake, including decision criteria and escalation pathways.
• You ensure poorly performing methods identified by CMV are documented, prioritised and routed into AMR governance.
• You maintain and manage an integrated CMV–AMR portfolio, aligned with risk, impact, capacity and annual objectives.
• You prepare and facilitate project boards, AMR steering meetings and risk reviews, including status, risks and mitigation actions.
• You support analytical data exploration and mapping (parameters, context, hierarchy, calculations) to feed CMV analysis and AMR root-cause hypotheses.
• You actively support QC sites through training, Q&A, problem solving and change execution related to CMV and AMR.

• You hold a Master's degree in Engineering, Chemistry, or Life Sciences.
• You have significant experience in QC systems (LES, SLIMS) to convert business needs into technical data and rules.
• You possess a strong background in analytical chemistry and QC environments.
• You bring proven experience in the pharmaceutical industry under GMP.
• You have demonstrated experience with analytical method performance monitoring, remediation or robustness initiatives.
• You have experience managing complex, multi-site programs across R&D, Development, or Industrial Operations.
• You demonstrate attention to detail, creativity, and excellent organisation and prioritization skills.
• You communicate and collaborate effectively with stakeholders.
• You are proficient in English.