Trabajos quality en Parets Del VallèsCrear alertas

Automation Engineer For our Grifols in Parets, we are looking for an Automation Engineer. This is a key hire for the successful implementation of a newly introduced equipment. We are seeking a professional with strong expertise and proven technical leadership skills. Main Requirements: • Minimum of 5 years of experience in industrial automation projects., • Advanced knowledge of Siemens TIA Portal and Siemens AWL Step7., • Hands-on experience with the commissioning of new machines/lines, troubleshooting, and process validation., • Desirable: knowledge of Rockwell and Zenon SCADA systems. Additional Skills (highly valued for this project): • Experience in the integration of equipment within GMP/pharma or other highly regulated environments., • Ability to prepare technical documentation and contribute to qualification processes (IQ/OQ)., • Strong team-player mindset to collaborate across engineering, maintenance, production, and quality teams., • Excellent problem-solving, analytical skills, and ability to liaise with external suppliers. This role will be essential in ensuring the successful start-up, optimization, and validation of the new machine, bringing expertise in both programming and systems integration. 📍 Location: Parets (Barcelona Area) Travelling may not be requiered at the begining but we need flexible travelling according the project is moving on -international-.

About the company: At Noucor we work on providing solutions to improve people's quality of life and contribute to a more sustainable world. We're a Spanish pharmaceutical company based in Barcelona and our business is focused on R+D, licensing, manufacturing, and the supply of pharmaceutical products. We have an extensive knowledge and experience offering quality products and solutions in the health ecosystem. We have an innovative focus with an industrial vocation with a fine chemical plant dedicated to the development and production of active pharmaceutical ingredients, a pharmaceutical plant manufacturing solid and semi-solid forms and a plant exclusively focused on food supplements. With 500 employees, we are present in over 100 markets being Japan, Canada and the EU key markets. Our culture promotes diversity, equality and inclusion and is committed to a new flexible and motivating leadership. We keep on building an organization in which people's experience is a means of engagement, attraction and development of talent, to always make people our focus and priority. Join the Legal Team at Noucor! We’re looking for a Legal Counsel. Are you ambitious and ready to take on a new challenge in a highly complex and responsible environment? If so, keep reading! Your challenges: • Participate in the negotiation of various types of contracts typical of the pharmaceutical industry, including drafting and reviewing confidentiality agreements, service agreements, licensing agreements, co-development, manufacturing and supply agreements, etc., • Provide legal advice to different areas of the company, such as Business Development, Clinical Affairs, Procurement, Regulatory Affairs, Marketing, and others., • Carry out administrative tasks, such as attending notary appointments and filing documents in the repository. What are we looking for? • Education: A degree in Law., • Experience: At least two years of experience in the legal department of a pharmaceutical company or a law firm advising companies in the sector., • Language skills: Professional proficiency in English, both spoken and written, is essential., • Profile: Enthusiasm for working in a multinational and innovative company. Passion for legal matters in international projects. We Offer: 🤩 Work within a great team of professionals with a very good work environment. ⚙️ Innovative work environment focused on continuous improvement. 🚀 Continuous learning and development. 💼 Competitive benefits package and flexible schedule. 📍 Offices in Palau-solità i Plegamans. 💰 Competitive salary. If this sounds like you, don’t miss the chance to embark on this exciting opportunity!

About Werfen Werfen is a global leader in specialized diagnostics, operating directly in over 30 countries and reaching more than 100 territories worldwide through distributors. We develop, manufacture, and distribute integrated solutions — including systems, reagents, automation, and software — for use primarily in hospitals and clinical laboratories. At Werfen, we are driven by innovation, precision, and collaboration. Our people are at the heart of everything we do, committed to advancing patient care through excellence in science and technology. What You’ll Be Doing: As a Maintenance Technician, you will be responsible for repairing and installing manufacturing and R&D equipment, ensuring all systems operate efficiently and safely. You will perform preventive maintenance according to manufacturer specifications, inspect equipment performance, and diagnose and correct malfunctions or technical issues as needed. Key Responsibilities: • Perform preventative maintenance on the assigned equipment, • Repair all production equipment as needed, • Perform breakdown analysis, • Perform general housekeeping, • Upgrade production lines with new equipment/technology, • Work with outside contractors working on assigned line, • Comply with GMP, safety, and audit standards, • Work independently under limited supervision (self-management), • Documentation of the work orders, • Collaborate on the improvements and optimization of the machines Networking/Key relationships: This position requires cooperation with: • Filling & Packaging Department, • Bulk and Intermediate Manufacturing Departments, • Engineering Minimum Knowledge & Experience required for the position: • Education: • Required: CFGM in maintenance, Mechanics, electronic, electric, or similar. Valuable: Any additional degree higher than that required in the previous section • Experience: • Depending on the type of laboratory to which the technician is going to be placed, specific experience may be required in topics like maintenance, Mechanics, electronic, electric. • Additional Skills/Knowledge • Software: Fluency in Office Tools (Excel & Word), and valuable basic knowledge in SAP., • Language: Fluency in Spanish or Catalan. Basic knowledge of English (reading and, • speaking). Skills & Capabilities: The ideal candidate for this position will exhibit the following skills and competencies: • Ability to maintain, calibrate and use technical equipment with accuracy, • Flexibility in order to work with and provide support for a number of people, • Teamwork, • Attention to detail, • Oral and written communication skills, • Reflects company values through the quality of work and professional relationships.

Desde Claire Joster Recruitment estamos en búsqueda de un/a PRODUCTION SPECIALIST para unirse a una compañía farmacéutica internacional de referencia: Esteve Química. Esteve Química es una empresa líder en el sector farmacéutico en España, con fuerte presencia internacional. Su compromiso con la innovación, la investigación y las alianzas estratégicas la convierten en un referente en la fabricación de ingredientes activos farmacéuticos (APIs) y productos intermedios. Con sede central y centro de I+D en Barcelona, cuenta con plantas de producción en Celrà, Lliçà de Vall y Banyeres del Penedès. La posición está ubicada en la planta de producción de Lliçà de Vall. Tu misión será dar soporte técnico, documental y formativo al Responsable de Producción en aquellas tareas que así se requiera en la planta. Tus principales responsabilidades incluirán: • Proponer soluciones y mejoras industriales de los procesos en la planta de LDV., • Seguimiento y soporte en la puesta en marcha de los nuevos procesos de producción., • Soporte técnico-administrativo al Responsable de Producción., • Soporte en la ejecución de las campañas industriales, teniendo en cuenta la planificación establecida por el Responsable de Producción y los Industrial Process Leaders (IPL)., • Formación del personal de planta de producción en nuevos procesos y operativas. -Participar en la elaboración de HAZOP de los procesos. • Preparación de Quality Risk Assessment de los procesos, entre otros documentos., • Colaborar en los traspasos de procesos desde y hacia otros centros de trabajo nacionales e internacionales., • Dar soporte técnico en auditorías e inspecciones de clientes y autoridades., • Back-up del jefe de turno en su ausencia. -Detectar, proponer e implantar mejoras en los procesos químicos de producción. -Redactar Hojas de fabricación, Hojas de limpieza y toda aquella documentación que proceda. -Preparar controles de cambios. -Preparar desviaciones de proceso. -Preparación y cumplimentación de documentación técnica de instalaciones (Protocolos, Cualificaciones). • Detectar y proponer soluciones a las necesidades de producción en relación a la mejora de equipos/instalaciones, inversiones, formación, Prevención y Medio Ambiente, etc. Requisitos: • Licenciatura en Ciencia Químicas o Ingeniería Química., • Catalán y Castellano., • Inglés nivel B2 (según MRCE)., • Experiencia en puesto similar en planta de producción, preferiblemente en el sector químico-farmacéutico. Formación complementaria en: • Cursos Normativa GMPs para APIs., • Cursos de Prevención y Medioambiente., • Office usuarios. Se ofrece: • Contrato temporal, aproximadamente de 20 semanas., • Beneficios sociales: subsidio de comedor, seguro colectivo, pluses adicionales., • Horario de turno continuo: mañana-tarde-noche, de lunes a viernes., • Salario competitivo. ¿Te interesa o conoces a alguien que encaje? ¡No dudes en compartir o aplicar!

About Werfen Werfen is a global leader in specialized diagnostics, operating directly in over 30 countries and reaching more than 100 territories worldwide through distributors. We develop, manufacture, and distribute integrated solutions — including systems, reagents, automation, and software — for use primarily in hospitals and clinical laboratories. At Werfen, we are driven by innovation, precision, and collaboration. Our people are at the heart of everything we do, committed to advancing patient care through excellence in science and technology. What You’ll Be Doing: As a Manufacturing Lab Technician, you’ll support the execution of manufacturing processes while ensuring compliance with quality, safety, and environmental standards. You’ll prepare materials, reagents, and equipment, carry out laboratory procedures and tests, record production data, and perform routine maintenance of lab instruments. Key Responsibilities: • Conducts manufacturing processes and laboratory tests according to approved instructions., • Operates a variety of laboratory equipment, • Compiles manufacturing data, performs the required calculations and complete the corresponding manufacturing and testing records., • Maintains a clean, sanitary and well resourced work area in accordance with approved practices and the regulations in place., • Follow strict laboratory, quality, safety and environmental procedures according to regulations in place., • Under the supervision of his manager and with the support -if needed- of other colleagues, can collaborate in the transfer & set up of new processes and systems., • Participates in activities related to continuous improvement, 5S and Lean Six-Sigma Requirements: Education: Vocational training (Ciclo Formativo de Grado Medio or higher) in a science or health-related field. Experience: Previous work in laboratory environments is essential. Experience in cell culture, molecular biology, biochemistry, lab automation, or clinical analyzers will be a plus. Experience in chemical, biological, or health laboratories will be highly valued. Equivalent experience can be considered in place of formal education. Languages: Fluency in Spanish or Catalan and a basic level of English (reading and speaking). IT Skills: Confident user of Microsoft Office (Excel, Word). Basic knowledge of SAP will be considered an advantage. Skills & Competencies: • Strong ability to operate, calibrate, and maintain laboratory equipment accurately., • Attention to detail and precision in daily work., • Team-oriented and flexible, able to support colleagues across different areas., • Good communication skills, both written and verbal., • Commitment to quality, safety, and continuous improvement in all tasks.

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Immunoassay business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. Within a medical device environment, work with the QARA Manager to ensure regulatory compliance and certification of software products. Key Accountabilities Be a key part of a team where you will: • Collaborate in maintaining the quality system documentation processes and procedures adopted by the company., • Investigate and resolve quality issues, implementing corrective and preventive actions to mitigate recurrence., • Coordinate and support the preparation of software technical documents appropriate for regulatory submissions., • Support the regulatory submissions for market authorization for medical device products., • Conduct internal assessments and audits to identify areas for improvement and ensure adherence to established procedures., • Facilitate the approval process for software releases., • Disseminating knowledge about the Quality System and regulatory requirements., • Review Promotional and advertising materials., • Oversee post-market surveillance activities related to medical device products., • Offer guidance and mentorship to QARA team members at lower levels Networking/Key relationships The main relationships within to the Werfen Group are: • QARA Manger, QA Leads, Validation Led, • Factory Lead and Solution Leaders, • Customer, • Application Lifecycle manager (ALM), • Notified Bodies and Competent Authorities for product regulatory compliance., • This position may also require also cooperating with other companies inside Werfen. Minimum Knowledge & Experience required for the position: • Engineer, computer Science or other Technical carrier, or equivalent work experience., • A minimum of 5 years experience in Quality Assurance or Regulatory related, preferably within the Healthcare sector, • Additional Skills/Knowledge:, • Knowledge and experience working with medical device international regulations and related standards (ISO 13485, ISO 14971,..)., • Knowledge and experience working in Medical device software life cycle process (IEC 62304), • Desirable:, • Knowledge and experience working in medical device regulatory submissions (MDR/IVDR,FDA..), • Internal auditor qualification for management systems or knowledge of auditing techniques Skills & Capabilities: The ideal candidate for this position will exhibit the following skills and competencies: • Good level of Technical and Conversional English., • Team player with ability to work independently., • Excellent and effective written and verbal communication skills., • Excellent interpersonal skills, good judgment and analytical skills., • Effective time management and organizational skills What we offer: • A meaningful project that will impact the quality of laboratory software medicine worldwide, • 3 days a week working from home, • Multicultural and friendly team, • Exciting opportunities for professional development., • Ongoing training, • Social benefits: Canteen, nursery check, English training..., • All the benefits according to the chemical agreement Our Purpose: We contribute to the advancement of patient care around the world through innovative specialized diagnostics JOIN US!

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