Automation Engineer - Expert in Supervision and Automation (F/H/X)

Role overview This Automation Engineer position at AbbVie Inc. is based in Martillac and centers on supervision and automation. The role is designed to improve automation processes and oversee the execution of projects, with a focus on supporting operational efficiency. Bringing new ideas and encouraging fresh approaches within the team are important aspects…

AbbVie seeks an Automation Engineer with advanced expertise in supervision and automation. This role is based on-site in Martillac and centers on ensuring the reliable operation of automated production systems. Role overview The Automation Engineer will monitor and supervise automation processes, working to keep critical systems running smoothly. The position involves hands-on oversight of production automation and active problem-solving to address issues as they arise. What you will do Supervise automation processes across production systems Troubleshoot and resolve automation-related issues to support consistent operations Identify workflow improvements and implement new automation solutions Requirements Solid background in automation technologies Proven experience supervising automated systems Drive to optimize processes and enhance efficiency This position requires presence at the Martillac site.

Join AbbVie as a Validation Expert for Computerized Systems (CS Expert) and play a pivotal role in ensuring compliance and excellence in our operations. This position requires an in-depth understanding of validation processes, regulatory requirements, and the ability to work collaboratively with cross-functional teams to ensure the integrity of our computerized systems.

OverviewIn response to an increased workload related to technical projects at the Martillac site, we are seeking a Technical Project Manager (TCE) to oversee a portfolio focused on processes and classified pharmaceutical areas.Key Projects Include:Installation of equipment and/or systems within a pharmaceutical setting (from identifying user needs to bringing installations into production).Engagement in classified production areas or analytical laboratories.Coordination of external interventions (from quotation to final internal reception).Facilitating communication regarding projects.Ensuring adherence to timelines.Providing transverse management of representatives from Quality Assurance, Qualification/Metrology, users, and maintenance teams.Contributing to the site's future by advocating for infrastructure enhancements (design studies: technical and financial evaluations of projected projects for the upcoming year and beyond).Your Role:Reporting to the Technical Project Supervisor within the Engineering Department, you will collaborate with all site resources, adhering to internal standards and deadlines.Main Activities Include:Researching existing data and conducting comprehensive assessments across all domains (technical, EHS, AQ, etc.) while facilitating external expert assessments as needed.Developing investment scenarios and leading their presentations.Conducting feasibility studies and detailed analyses of multi-disciplinary projects while producing project documentation (CCTP, graphical documents, etc.).Defining, consulting, and managing external engineering services throughout all project phases.Leading calls for tenders, aligning technical offers, and finalizing with the purchasing department.Managing construction sites in occupied areas or enclosed sites (personnel flow management, utility outages, and site communication organization).Overseeing project budget tracking (initial consolidation, management of forecasts, orders, and real-time reception).Promoting safety on sites (with an objective of zero accidents).Facilitating the transfer of installations to users.Optionally: proficiency in illustrating technical solutions using AutoCAD (PID, layout plans, etc.) or Visio for functional flowcharts.

Join our dynamic production team at AbbVie, where you will play a vital role in our DSP (Downstream Processing) unit, focusing on the purification of recombinant proteins intended for large-scale production under GMP (Good Manufacturing Practices) conditions.Key Responsibilities:As part of our pharmaceutical production setup utilizing single-use equipment, you will be responsible for:Preparing purification activities, including qualification of equipment, ensuring availability of buffers, materials, and assembly setups.Documenting manufacturing recipes by entering production parameters into a computerized system (quantities, durations, temperature settings, addition sequences, etc.) to facilitate automatic or semi-automatic execution of production recipes.Maintaining cleanliness and organization in the production area in compliance with good manufacturing practices and internal procedures.Cleaning and packaging the columns used for purification processes.Executing purification activities will involve:Setting up single-use production kits.Conducting DSP operations either manually or through computerized recipes.Implementing chromatography techniques, depth filtration, tangential flow filtration, and dialysis.Ensuring traceability of activities performed in relation to the batch records.Reporting deviations as necessary.Maintaining the cleanliness of the production area.Monitoring DSP production activities includes:Reviewing work sheets and post-activity reports.Data compilation and participation in technical investigations.This position requires flexibility to work in rotating shifts (morning/afternoon) under the supervision of the DSP team leader.

Join AbbVie, a global biopharmaceutical company, as a USP Technician (F/H/X) in Martillac. In this role, you will be an integral part of our team, responsible for ensuring the highest quality standards in our manufacturing processes. As a USP Technician, you will engage in various technical tasks that support the production of our innovative pharmaceutical products.

Join AbbVie, a global biopharmaceutical company, as a Quality Specialist. In this role, you will be responsible for ensuring that our products meet the highest quality standards. Your expertise in quality control and compliance will be critical to our success in delivering innovative solutions to patients worldwide.

Primary Mission: Operation and Maintenance ManagementExecute preventive, corrective, and improvement maintenance operations on equipment utilized in clinical and commercial production.Provide expertise and technical support for laboratory equipment maintenance challenges.Ensure the qualification status of all equipment and installations within your area of responsibility.Monitor maintenance contracts and third-party service providers for all equipment in your scope, overseeing routine operation and planned technical shutdowns.Secondary Mission: Equipment ManagementEnsure traceability of interventions by documenting actions taken on equipment in accordance with site GMP regulations, maintaining logs in equipment logbooks and maintenance management systems (GMAO).Update and review technical and quality documentation for all equipment in your responsibility.Propose and implement improvement and optimization actions for equipment.Manage procurement and inventory of parts necessary for maintenance operations.On-Call Duty ResponsibilitiesOversee alarm management and necessary actions during on-call duty (as per site agreement).Provide technical support during on-call periods, focusing on general infrastructure (HVAC, purified water systems, compressed air, air handling units, and effluent treatment).Diagnose and troubleshoot technical installations (utilities, production equipment, automation) with assistance from duty team members.Address alarms via supervision systems and intervene on-site or remotely based on the incident's nature.Evaluate technical impacts and secure installations as necessary.Document interventions in the GMAO and on-call reporting tools.Communicate effectively with technical and operational teams.Participate in on-call rotation with the capability for rapid on-site intervention.

Join AbbVie, a global biopharmaceutical company, as a Quality Control Technician. In this role, you will play a crucial part in ensuring the quality and safety of our products. You will be responsible for conducting tests, analyzing results, and maintaining compliance with industry standards. Your meticulous attention to detail will contribute to our commitment to delivering innovative medications that improve patients' lives.

Join AbbVie as a Team Leader USP (F/H/X), where you will spearhead the USP team in Martillac. Your leadership will drive excellence in our operations, ensuring adherence to the highest standards of quality and compliance. You will oversee daily activities, manage team performance, and collaborate with cross-functional teams to enhance productivity and efficiency.

Join AbbVie as an Operational Maintenance Technician (F/H/X) in Martillac, where you'll play a crucial role in ensuring the functionality and efficiency of our manufacturing equipment. As part of our dedicated team, you will be responsible for conducting routine maintenance, troubleshooting issues, and implementing solutions to enhance operational performance.

Join AbbVie as a Team Leader in Digital Supply Chain (DSP), where you'll lead a dynamic team responsible for optimizing our supply chain processes. This pivotal role involves overseeing operations, ensuring efficiency, and driving innovation within the DSP framework.

AbbVie in Martillac offers an apprenticeship for a Microbiology Technician (F/H/X). This position provides hands-on training in microbiological methods and laboratory procedures within a biopharmaceutical environment. Role overview This apprenticeship focuses on developing practical skills in microbiology. The technician apprentice will learn to support daily lab activities and apply microbiological techniques relevant to biopharmaceutical production. What you will do Assist with laboratory processes and routine microbiological testing Gain experience working in a biopharmaceutical lab Follow established protocols and safety standards Requirements Interest in microbiology and laboratory work Willingness to learn in a structured apprenticeship setting Ability to work on-site in Martillac

About the Role AbbVie Inc. is seeking an Occupational Therapy Technician (F/H/X) for its Martillac location. This position supports occupational therapy services and helps maintain high standards of patient care and rehabilitation. What You Will Do Assist occupational therapists in daily patient care activities Support rehabilitation programs as directed by healthcare professionals Contribute to a collaborative care environment focused on patient well-being Location Martillac

About the Role AbbVie Inc. is seeking an Occupational Therapy Technician (F/H/X) for its Martillac location. This position supports the delivery of therapeutic services, working closely with clients as they pursue better health and well-being. What You Will Do Assist occupational therapists in daily activities and therapy sessions Support clients during their rehabilitation process Help maintain therapy equipment and prepare materials for sessions Who Should Apply This role suits individuals interested in starting a healthcare career and making a difference in patient outcomes. Previous experience is not required, but a genuine interest in patient care is important.

Join AbbVie as a Quality Control Supervisor where you will play a crucial role in maintaining the highest standards of quality and compliance within our laboratory environment. In this position, you will oversee quality control operations, ensuring adherence to regulatory standards and internal policies. Your keen attention to detail and leadership will guide your team in executing testing procedures and validating results. This is an exciting opportunity to contribute to our mission of improving patient outcomes through innovative solutions.

AbbVie is seeking a dedicated Quality Control Supervisor to join our dynamic team in Martillac. This role is ideal for individuals looking to start their career in the pharmaceutical industry. As a Quality Control Supervisor, you will play a crucial role in ensuring that our products meet the highest quality standards. Your responsibilities will include supervising quality control processes, conducting inspections, and collaborating with cross-functional teams to maintain compliance with regulatory requirements.

As the Senior Customs Compliance Analyst for France, you will play a vital and strategic role within our team, ensuring adherence to international trade laws and local regulations while enhancing operational efficiency and reducing tariff and non-tariff barriers. This position will primarily focus on our Martillac site, while also providing support to another key site in France (Pringy) and other EU locations as needed, with tactical and compliance activities.Leveraging your expertise and collaborating with various cross-functional teams, you will aid in optimizing trade compliance operations, enhancing decision-making processes, and mitigating risks. Your contributions will be critical in shaping the future of our trade compliance function and supporting AbbVie's mission to improve the lives of individuals globally.Key Responsibilities:Establish and maintain local import and export operational procedures.Engage with local site management and other internal/external partners to ensure all import/export transactions comply with EU customs legislation.Act as the primary contact with customs and any other government agencies to respond to audit and inspection requests. Provide support for external reviews and audits to minimize any negative impact on the business.Manage daily import/export operations and resolve daily customs-related issues that may cause border delays.Oversee trade financial and operational indicators and analysis, developing solutions/strategies for issues or opportunities.Conduct training and share knowledge to enhance business acumen and operational performance while ensuring compliance with import/export regulations.Collaborate with our customs broker and support the management of the relationship and performance in France.Evaluate and initiate import/export customs management projects and/or any Special Trade Programs aimed at improving efficiency or reducing costs (e.g., customs processing).Monitor and align with relevant GTC partners regarding regulatory and legislative changes in trade compliance that could impact our manufacturing operations, alerting appropriate internal parties to potential business impacts.Support the site when licenses/permits/authorizations from other government agencies are required for import and export activities.

Rejoignez notre équipe de production en tant que Technicien Purification, où vous intégrerez l'équipe DSP dédiée à la purification de protéines recombinantes, essentielles pour la production à grande échelle dans un environnement GMP.Vos missions incluront :Préparation des activités de purification, incluant la qualification des équipements et la vérification de la disponibilité des matériaux nécessaires.Rédaction des recettes de fabrication : saisie des paramètres de production dans un système informatisé pour garantir une exécution optimale.Gestion de la zone de production : organisation, nettoyage et respect des bonnes pratiques de fabrication.Réalisation des activités de purification : installation des kits de production en single-use et conduite des opérations DSP.Mise en œuvre des techniques de purification, y compris chromatographie, filtration et dialyse.Suivi rigoureux des activités, incluant la traçabilité et la compilation des données.Ce poste se déroulera en rotation (matin/après-midi) sous la supervision du chef d'équipe DSP.

Join AbbVie as a Technicien USP (F/H/X) in Martillac, where you will play a crucial role in ensuring the efficiency and effectiveness of our production processes. You will be part of a dynamic team dedicated to advancing healthcare through innovative solutions.