Production Operator - Material Sampling

Join AbbVie, a global biopharmaceutical company, as a Production Operator specializing in Material Sampling. In this dynamic role, you will be responsible for ensuring the quality and integrity of our materials used in the manufacturing process. Collaborate with a dedicated team to maintain high standards and contribute to our mission of delivering innovativ…

Join AbbVie, a global biopharmaceutical company committed to discovering and delivering innovative medicines. As a Production Operator specializing in Material Sampling, you will play a pivotal role in our manufacturing process by ensuring the quality and integrity of materials used in production. This position offers a unique opportunity to contribute to life-changing therapies while working in a dynamic and collaborative environment.

Join AbbVie, a global biopharmaceutical company, as a Production Operator specializing in material sampling. In this role, you will be responsible for the effective sampling of materials to ensure the highest quality standards in our production processes. Your contribution will be crucial in maintaining our commitment to excellence in product safety and efficacy.

Join AbbVie, a global biopharmaceutical leader, as a Production Operator specializing in material sampling. In this dynamic role, you will be instrumental in ensuring the quality and efficiency of our production processes. Your responsibilities will include conducting material sampling, performing quality checks, and collaborating with team members to uphold our commitment to excellence.

AbbVie is seeking a Production Flow Operator (PFO) to join its team in Martillac. This entry-level role plays a key part in supporting daily manufacturing activities by tracking and managing how materials and products move through each stage of production. The work directly contributes to maintaining efficient operations and upholding product quality standards. Key responsibilities Monitor production lines and processes to ensure smooth operation Manage the flow of materials and finished products through various manufacturing stages Assist in meeting established quality and efficiency targets Who will thrive in this role This position is well suited for individuals beginning a career in the pharmaceutical sector. Prior production experience is not required. Success in this role depends on strong attention to detail and a reliable work ethic.

AbbVie Inc. seeks a Production Flow Operator (PFO) (F/H/X) for its Martillac facility. This position plays a key part in daily production, assisting with tasks that keep manufacturing running smoothly. Role overview The Production Flow Operator supports routine operations on the manufacturing floor. Work centers on helping production teams meet daily targets and ensuring processes remain efficient. Career development This entry-level role is designed for those interested in developing a career in the pharmaceutical industry. It provides hands-on experience in a regulated production environment.

Join our Quality Control team at AbbVie, where you will be instrumental in ensuring the quality of raw materials used in our production processes. Under the guidance of the Microbiology and Raw Materials QC Manager, you will perform sampling and analysis in a highly regulated environment adhering to GMP (Good Manufacturing Practices) standards.Key Responsibilities:1. Sampling of Raw MaterialsPrepare sampling campaigns and conduct sampling of raw materials and gases.Ensure the supply of consumables for the sampling area.Contribute to maintaining the overall cleanliness and organization of the sampling area.Assist in tracking materials internally or with subcontractors, including verifying Certificates of Analysis (CoA).Coordinate with the logistics team for the preparation and shipment of raw materials for analytical subcontracting.2. Participation in Material ReleaseCarry out the release of consumables in SAP according to established procedures.Support activities related to sample management, including sample identification verification and periodic inventory participation.Open deviations (exception reports) related to material release activities.Notify Quality Assurance and/or management of any blocking issues or non-compliance.3. Conduct QC Analyses on Raw MaterialsPerform identification analyses for specific raw materials.Verify laboratory data (logbook and double-check raw data).Ensure analyses are performed on qualified and calibrated equipment.Draft standard operating procedures, user manuals, and analytical protocols.Contribute to maintaining the overall appearance of the laboratory.4. Monitoring, Documentation, and QualityMaintain rigorous traceability in analytical documents and quality systems.Open non-compliance events in the dedicated software and participate in laboratory investigations related to performed analyses.5. Work Schedule and OrganizationWork in rotating shifts: morning and afternoon.

Join our Quality Control team at AbbVie, where you will play a crucial role under the guidance of the Microbiology and Raw Materials Quality Control Manager. Your primary responsibilities will include sampling and analyzing raw materials utilized in our production processes. You will thrive in a high-quality environment adhering to GMP standards.Key Responsibilities1. Sampling of Raw MaterialsPrepare sampling campaigns and perform sampling of raw materials and gases.Ensure the supply of necessary consumables for the sampling area.Contribute to maintaining the overall appearance of the sampling area.Assist in monitoring raw materials internally or with subcontractors, including verification of Certificates of Analysis (CoA).Liaise with the logistics team to facilitate the preparation and shipment of raw materials for analytical subcontracting.2. Participation in Material ReleaseExecute the release of consumables using SAP in compliance with current procedures.Support activities related to the management of the sample library (sample identification verification, participation in periodic inventories, etc.).Open deviations (exception reports) related to material release activities.Notify Quality Assurance and/or management about any blocking points or non-conformities.3. Conduct Quality Control Analyses on Raw MaterialsPerform identification analyses on specific raw materials.Verify laboratory data (logbook / double-check raw data).Ensure that analyses are conducted on qualified and calibrated equipment.Draft operational procedures, user manuals, and analytical protocols.Participate in maintaining the overall appearance of the laboratory.4. Tracking, Documentation, and QualityMaintain rigorous traceability on analytical documents and quality systems.Open non-conformity events in the designated software and conduct/participate in laboratory investigations related to the analyses performed.5. Schedule and OrganizationWork in a morning/afternoon shift rotation.

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 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.

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 as a Technician in Bio Production, where you will play a pivotal role in our biopharmaceutical manufacturing processes. You will be responsible for ensuring the quality and efficiency of our production lines while adhering to strict safety and regulatory standards. Your expertise will contribute to the development of life-saving medications that make a difference in patients' lives.

Join our dynamic production team at AbbVie, where you will play a crucial role in the preparation of culture media and buffer solutions (PMT) required for the large-scale production of recombinant proteins for client projects under GMP conditions.Your key responsibilities include:Preparing for PMT activities:Ensuring the qualified status of equipment and verifying operational needs before launching activities according to the defined schedule.Managing line clearance, organizing, and maintaining the production area in compliance with Good Manufacturing Practices (GMP) and internal procedures.Executing PMT activities:Weighing raw materials needed for culture media and buffer preparations.Preparing culture media and buffer solutions in a controlled atmosphere environment (Class D).Conducting sterilizing filtration of the preparations.Maintaining traceability of completed activities in relation to the batch records.Initiating deviations when necessary.Maintaining the production area.Monitoring PMT production activities:Reviewing work documentation and conducting post-activity reviews.Compiling data and participating in technical investigations and continuous improvements.This role will involve rotating shifts (morning/afternoon) and is based in Martillac (33), available as a permanent contract (CDI) as soon as possible (35 hours per week).

Join our dedicated production team at AbbVie, where you'll play a critical role in preparing culture medium and buffer solutions (PMT) essential for the large-scale production of recombinant proteins for client projects under GMP conditions.Your key responsibilities will include:Preparation for PMT activities:Verification of equipment qualifications and operational needs prior to activity commencement as per the established schedule.Line clearance, organization, and maintenance of the production area in compliance with GMP and internal procedures.Execution of PMT activities:Weighing of raw materials necessary for the preparation of culture media and buffers.Preparing culture and buffer solutions in a controlled atmosphere area (Class D).Performing sterilizing filtration of preparations.Ensuring traceability of activities related to the batch record.Reporting deviations as necessary.Maintaining the production area.Monitoring PMT production activities:Reviewing work instructions and post-activity reviews.Data compilation and participation in technical investigations and continuous improvement initiatives.This position involves working in shifts (morning/afternoon) and is located in Martillac (33), available as a permanent contract (35 hours/week) as soon as possible.