Descripción de la oferta
pbAbout the role /b /ppbr/ppAs Analytical Manager under supervision of the RD Director will be responsible for management of the analysis area of the research and development (RD) department taking responsibility for the management of the planning, research/development, monitoring and implementation of new projects, CDMO or off-patent, as well as the improvement of existing ones, at the laboratory level in Uquifa Spain, to guarantee safety, quality, compliance with planning and agreed costs, following the quality, safety and environmental regulations established in the company and providing innovative solutions to the processes and working methods whenever possible. /ppDetermine what technical and personal resources are needed to be able to carry out the projects in a timely manner according to the client's needs, from the beginning of the RD to the implementation in the QC department by transferring the project. /pp Participate together with the QC Manager and Project Manager in the planning of the actions of the Quality Control Department to meet the requirements of the CDMO projects. /ppDirect dialogue with the clients of CDMO projects, both new implementation and regular production, collecting needs and updating the status of the actions to transfer them to RD and/or QC. /ppSupport the Regulatory Affaris department in responding to deficiency letters and define what related activities are needed to be executed through the RD Analytical Leader. /ppbr/ppbr/ppbDuties: /b /ppbr/pulliManage the analysis team of the Uquifa Spain RD department. Compliance with the approved Budget. /liliDefine processes in which RD analysis intervenes through instructions, clearly identifying the responsibility for the different activities. /liliOnce new projects are approved, evaluate and allocate RD resources for the execution of the analytical stages of the projects assigned to the department. /liliManage the analytical activities associated with the projects, and monitor their execution, reallocating resources, if necessary, to guarantee safety, quality, deadlines and agreed costs. /liliReview and/or approve analytical documentation associated with projects that is generated in the RD department. /liliEnsure the transfer of technical-scientific knowledge between the RD and Quality Control departments. /liliCollect the necessary technical information during the plant scale-up process. /liliTo manage analytical activities derived either from the Defficiency Letters received from our records, or from the regulatory requirements of our clients. /liliManage the performance of the analytical activities derived from the risk assessment of processes according to ICH M7 standard, develop the analytical methods for their detection if necessary. /liliCoordinate analytical activities of the RD Department with the rest of the company's departments. /liliContribute to the HAZOP's studies with the analytical part for new processes and/or new products. /li /ulpbr/ppbExperience and attributes we value /b /ppb1. Technical Background /b /pulliDegree in Chemistry or related field (PhD highly preferred) /lili5–10 years of experience in analytical development /liliExpertise in techniques such as HPLC, GC, LC-MS/MS /liliStrong knowledge of method validation (ICH guidelines), stability studies, and analytical transfers /liliExperience in regulated environments (GMP/GLP) /li /ulpb2. Problem-Solving Critical Thinking /b /pulliAbility to design analytical strategies, not just execute methods /liliStrong troubleshooting skills and data-driven decision-making /li /ulpb3. Leadership Skills /b /pulliProven experience managing teams /liliAbility to prioritize, delegate, and develop talent /liliStrong communication and conflict resolution skills /li /ulpb4. Project Business Awareness /b /pulliExperience working cross-functionally (QA, Production, Regulatory) /liliUnderstanding of timelines, costs, and product development lifecycle /li /ulpbr/ppbWhat’s on offer /b /pulliPermanent contract /liliFixed salary plus bonus /liliFlexible working hours /liliRemote working (1 day a week) /li /ul
