Save Job Back to Search Job Description Summary Similar Jobs added 28/01/2025International, pharmaceutical company12 months contract with extension optionAbout Our ClientOur client, an internationally renowned pharmaceutical company is recruiting. On its behalf we are now looking for a Senior Expert Manufacturing for USP starting in February for Solothurn area, to join their international team for a period of 12 months.Depending on the selected candidate's performance and motivation, there is a possibility of an extension or a permanent take over.Job DescriptionThe Manufacturing Expert will be responsible for technical and scientific support to manufacturing (MFG) shopfloor and will manage timely completion of MFG activities (compliance, TT, campaign preparation, troubleshooting…). The responsibilities will be around the following task areas:Acting as Subject Matter Expert on manufacturing equipment and automated processes (Upstream Drug Substance Biologics)Partnering with direct manager to assign appropriate resources to tech transfers, drive continuous improvement, ensure manufacturing instructions are clear, safe, and compliantOpportunity to coach and train cross functionally to meet career goals and business objectives AND to be individual contributor with respect to technical instruction management for specific portions of a manufacturing processInitiating, owning, and managing Manufacturing focused Change Controls, CAPAs, and Planned ExceptionsContinuous improvement and Coaching of Manufacturing Associates regarding main area of expertise and side processesIncreasing productivity - managing intra, cross-site, and cross-functional projects related to process and productivity improvementsThe Successful ApplicantIn order to be considered for the role, the selected candidate must have:Bachelor or higher degree in Engineering or related field8+ years work experience within GMP environmentUpstream Experience ideally for Drug Substance of BiologicsStrong manufacturing/technical process knowledge and/or strong knowledge of scientific principlesStrong understanding of basic QA and cGMP principlesCoaching and Trainer skills for Manufacturing related activities (as Deputy to the MTO Manager)DeltaV experience is a MUST, Syncade is a nice to haveStrong documentation and communication skills in English to interact with a cross-functional team effectivelyWhat's on OfferThe selected candidate will be part of a dynamic team and actively contribute to the discovery, development and delivery of innovative therapies to improve the lives of patients.ContactKamila FotiouQuote job refJN-012025-6647504Job summaryJob FunctionHealthcare & Life SciencesSpecialisationBiotechnologyIndustryHealthcare / PharmaceuticalLocationSolothurnContract TypeInterimConsultant nameKamila FotiouJob ReferenceJN-012025-6647504
