Solid Packaging Technician

• Degree in Engineering and/or similar or Health Sciences such as Pharmacy or Chemistry.
• Minimum 2-3 years of experience in a similar position within the pharmaceutical sector.

• Fluent level of English, both oral and written, is essential, equivalent to First Certificate or higher.

• Deep knowledge of GxP regulations is highly valued.

• Training in continuous improvement tools.

• Knowledge of management tools such as TW, ManGo, HR4You Learning, or equivalent systems.

• Communication, collaboration, and teamwork skills.

Apply your Magic with us

Are you ready to explore, break barriers, and discover much more? We know you have big plans. We do too; innovating with science and technology to enrich people's lives with solutions in Healthcare, Life Science, and Electronics is what passions our colleagues around the world. Together, we dream big and share the enthusiasm for caring for a great diversity of people, customers, patients, and the planet. That is why we are always looking for curious minds who imagine the never-before-seen with us.

United as one for patients: our goal in Healthcare is to help create, improve, and extend lives. We develop intelligent treatments, devices, and innovative technologies in therapeutic fields such as oncology, neurology, and fertility. Our teams collaborate across 6 continents with passion and relentless curiosity, aiming to support patients at every stage of their lives. Joining our Healthcare team means becoming part of a diverse, inclusive, and flexible work culture that offers fantastic opportunities for personal and professional growth around the world.

• Ensure the correct application of legal regulations regarding the manufacture of pharmaceutical specialties, in accordance with established procedures regarding quality, GMP environment, safety, and the environment.

• Manage aspects linked to product quality, including deviations, change controls, equipment and cleaning validations, process controls, statistical sampling (AQL), and any other actions derived from process incidents.

• Under the supervision of the person responsible for the department and in coordination with the Quality area, ensure the continuity of processes safely, documenting actions when appropriate in the Quality management module.

• Supervise and analyze the monitoring of area indicators to contribute to the achievement of established objectives.

• Manage and communicate the information necessary to facilitate decision-making and the implementation of corrective actions that guarantee the optimal functioning of the department.

• Act as a liaison point between the team and the department management, channeling needs, proposals, and concerns from both parties.

• Diagnose and resolve incidents related to machinery, product, materials, or processes that may affect productivity or product quality.

• Review batch documentation after production and before the final review by Quality Assurance.

• Register the necessary batch data in the computer systems for continuous monitoring.

• Train and support the work team, facilitating their training and development for the correct performance of the tasks and responsibilities associated with the position.

• Monitor the daily activity of the team to ensure compliance with the quality and productivity standards established by the department.

• Under the supervision of the person responsible for the department and within their scope of action, manage and resolve incidents related to team members.

• Prepare the documentation necessary for the correct functioning of the department and for the adequate manufacture of products (procedures, cleaning methods, manufacturing guides, machinery instructions, among others), as well as provide the corresponding training to the personnel involved.

• Supervise and keep the training matrix of the area personnel up to date.

• Collaborate from a technical perspective in continuous improvement initiatives, providing proposals that contribute to the permanent evolution and optimization of the area.

• Participate in and lead continuous improvement projects, included in the area's TIP or cross-functional site scope, when required.

• Perform technical supervision tasks and participate in the acquisition of equipment, formats, or auxiliary materials, managing the associated documentation (purchase requests, among others) and performing the corresponding follow-up until their commissioning.

• Perform technical supervision of the area's formats when necessary, including the management of the associated database, verifying their correct status and promoting, when appropriate, the acquisition of new formats.

The person holding this position will collaborate cross-functionally with the Quality, Safety, Warehouse, Engineering, Purchasing, Supply Chain, and Pharmaceutical Technology areas as necessary for the performance of their responsibilities.

Permanent contract

Location: Mollet del Vallès.

• Orientation toward the needs and expectations of internal and external customers (Collaboration / Determination).

• Capacity for collaboration within the team and throughout the organization (Collaboration).

• Active contribution to the innovation of processes, services, and products, promoting sustainable improvements in the work environment (Innovation).

• Willingness to contribute to the achievement of ambitious objectives, driving continuous performance improvement through clear communication, results orientation, and constructive feedback (Results orientation).

• Capacity to identify opportunities for simplification and improvement of processes and work routines within their scope of responsibility (Innovation).

• Interest in continuous learning and professional development through the assumption of responsibilities and participation in additional initiatives (Commitment).