Senior Process Engineer

Barcelona Permanente Ver descripción del puesto
We are seeking a Senior Process&Project Engineer to join a pharmaceutical manufacturing facility located in Vallès Occidental. The role involves supporting aseptic filling operations (technical support, optimization, improvement and projects).

Added 08/08/2025

  • International pharmaceutical company with a new plant in the area of Barcelona
  • Project with high impact in the company and visibility

¿Dónde vas a trabajar?

Are you ready to take part in building something new from the ground up? A well-established and internationally expanding pharmaceutical company is setting up a manufacturing and R&D facility in Vallès Occidental (Barcelona) - and we're looking for a Senior Process&Project Engineer to play a key role in this journey.

The new site will operate as a Contract Manufacturing Organization (CMO), specializing in aseptic filling of generic and biosimilar products. In addition, the company will conduct R&D activities and manage technology transfer and FDF imports into EU markets from third countries.

Descripción

🌟 What You'll Be Doing:

  • Provide technical expertise and support for aseptic filling operations, including process troubleshooting, optimization, and improvement initiatives.
  • Provide technical support and expertise for aseptic filling operations, including vial and prefilled syringes filling, isolators, lyophilization, capping and packaging.
  • Perform data gathering, root cause analysis, and performance trending to develop appropriate process control changes for complex issues.
  • Prioritize and implement process change requirements based on the critical project needs.
  • Lead change management system for process changes or new processes and equipment.
  • Collaborate with cross-functional teams, including manufacturing, quality, and validation, to develop and implement process improvements, ensuring optimized and efficient manufacturing operations, as well as compliance with regulatory requirements and industry best practices.
  • Perform product complaint assessments and or investigations, and other related post-market surveillance activities.
  • Identify and resolve technical issues related to equipment, processes, and quality deviations.
  • Conduct process investigations and root cause analyses to identify and address deviations, non-conformances, and other process-related issues, implementing corrective and preventive actions as necessary.
  • Develop and implement process control strategies to improve product quality, yield, and efficiency.
  • Collaborate with cross-functional teams to develop and implement process improvements, ensuring optimized and efficient manufacturing operations.
  • Utilize Lean Production System elements and methods to continuously improve Engineering tactical business processes and procedures.
  • Participate in process validation activities, including protocol development, execution, and report writing.
  • Support equipment qualification and commissioning activities for new manufacturing equipment or processes.
  • Participate in technology transfer activities from development to commercial manufacturing, ensuring successful scale-up and process validation.
  • Support regulatory inspections and audits by providing technical expertise and documentation.
  • Foster an environment that encourages continuous learning. Maintain expertise as necessary to stay abreast of technical and industry advancements, and best practices related to aseptic processing.
  • Provide technical training and guidance to manufacturing personnel on aseptic techniques, equipment operation, and process controls.

¿A quién buscamos (H/M/D)?

🎓 What We're Looking For:

  • Bachelor's degree in Chemical or Mechanical Engineering, or a related field.
  • Minimum of 5 years of experience in aseptic manufacturing operations in the pharmaceutical industry
  • Strong knowledge of aseptic processing principles. Equipment and utilities, cGMP regulations, and regulatory requirements (e.g., FDA, EMA).
  • Experience with aseptic filling equipment and processes, such as isolators, filling machines, lyophilizers, and sterilization.
  • Experience with aseptic formulation and cleaning processes , equipment and utitilities needed such as vessels, autoclaves, visual inspection.packaging
  • Proficient in data analysis and statistical tools for process monitoring and optimization.
  • Excellent problem-solving and troubleshooting skills, with the ability to identify root causes and implement effective corrective actions.
  • Strong communication and collaboration skills, with the ability to work effectively in a cross-functional team environment.
  • Detail-oriented, with a commitment to ensuring compliance and delivering high-quality results.

¿Cuáles son tus beneficios?

🎁 What We Offer:

  • A unique opportunity to be part of the launch and growth of a brand-new pharmaceutical facility in Spain.
  • Collaboration with experienced professionals and strategic partners across Europe's pharmaceutical industry.
  • Competitive salary, aligned with your skills and experience.
  • Fixed contract.
Ver más ofertas de empleo
Belen Castaño
Indicar número de referencia para la oferta
JN-082025-6808867

Resumen de empleo

Sector
Ingenieros
Sub Sector
Gestión de Proyectos
Añadir industria
Industrial / Manufacturing
Localización
Barcelona
Tipo de Contracto
Permanent
Nombre del consultor
Belen Castaño
Número de referencia
JN-082025-6808867

En Michael Page creemos en la diversidad e inclusión. Defendemos la igualdad de oportunidades sin discriminar por género, raza, edad, religión ni orientación sexual o por cualquier otro aspecto que pudiera ser considerado excluyente.