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Sobre la empresa Compañía del sector farmacéutico, especializada en el acondicionado secundario farmacéutico y en la fabricación de productos sanitarios. La empresa trabaja bajo los más altos estándares de calidad y normativa ISO, colaborando con clientes nacionales e internacionales. Qué ofrecemos • Contrato estable e integración en un equipo experto y consolidado., • Entorno técnico en crecimiento, con alto componente normativo., • Formación continua en calidad y procesos farmacéuticos. Descripción del puesto El/la Quality Control (QC) será responsable de garantizar que todos los productos y procesos cumplen con los estándares de calidad internos y normativos antes de su liberación. Se incorporará al laboratorio, trabajando de manera transversal con producción, laboratorio y otros departamentos para asegurar la seguridad, eficacia y trazabilidad de los productos. Se requiere un enfoque práctico de laboratorio, incluyendo recepción y revisión de materias primas y productos, control organoléptico, homologación de proveedores y verificación de especificaciones antes de su uso en producción. Funciones principales • Control organoléptico de productos intermedios y terminados (aspecto, olor, textura y características sensoriales)., • Recepción y control de materias primas y productos, asegurando cumplimiento de especificaciones y normas de calidad., • Realizar inspección, pruebas analíticas y controles organolépticos de productos intermedios y terminados., • Participar en homologación y seguimiento de proveedores, garantizando la calidad de los materiales recibidos., • Registrar y documentar resultados de pruebas, incidencias y acciones correctivas en los sistemas internos., • Detectar no conformidades y colaborar en la implementación de acciones correctivas y preventivas., • Participar en auditorías internas y externas, asegurando la correcta trazabilidad de los productos y procesos., • Apoyar en procesos de mejora continua para optimizar estándares de calidad y procedimientos operativos. REQUISITOS Formación: • Titulación en Ciencias, Farmacia, Biotecnología, Química o similar. Experiencia: • Experiencia previa en control de calidad, laboratorio o procesos farmacéuticos (deseable, no siempre obligatoria)., • Experiencia en entornos normativos y regulados (ISO, GMP) valorable. Conocimientos y habilidades: • Conocimiento de procedimientos de calidad, normativa ISO y control de laboratorio., • Capacidad para realizar control organoléptico de productos y seguimiento de homologación de proveedores., • Manejo de instrumental de laboratorio y técnicas básicas de control de calidad., • Dominio de informática a nivel usuario y herramientas de registro/documentación., • Organización, atención al detalle y rigor en el trabajo diario., • Trabajo en equipo, proactividad y capacidad de comunicación., • Valorable inglés hablado y escrito. Competencias deseadas • Capacidad de análisis y resolución de problemas., • Orientación a mejora continua y aprendizaje en entornos normativos., • Flexibilidad y adaptabilidad a cambios en procedimientos y proyectos.

¿Buscas un puesto estable? ¿Aportas experiencia en calidad en compañías fabricantes de materia prima farmacéutica o producto terminado para farmacia? ¿Te gustaría trabajar en una importante empresa del sector químico farmacéutico, dedicada al desarrollo y fabricación de principios activos, ubicada en Montmeló? Si tu respuesta ha sido positiva, no lo dudes e ¡inscríbete! Se trata de un puesto ESTABLE, e incorporación DIRECTA por empresa. Horario: de lunes a viernes de 8 a 17h. Salario entre 40.000 y 45.000 €/a. Negociable en función del perfil aportado. Tu función principal será colaborar en la optimización y mejora de los sistemas de calidad vigentes, así como los procedimientos generales de calidad implantados en la empresa. Para ello, colaborarás con el Responsable de Garantía de Calidad, realizando entre otras, estas funciones: Revisión de la documentación de fabricación. Investigación, documentación de informes relacionados con las desviaciones críticas. Investigación, documentación de informes relacionados con las reclamaciones de clientes por motivos de calidad. Preparación y realización de autoinspecciones. Preparación y realización de auditorías de clientes o de autoridades regulatorias. Control y seguimiento de la implementación de acciones correctoras. Preparación y revisión de protocolos e informes de validación de proceso o de métodos de limpieza de equipos. Revisión de documentación para la aprobación de proveedores. Revisión de documentación para la aprobación de cambios. Mantenimiento de los programas de calibración de equipos críticos. Evaluación y edición de informes relacionados con los programas de estabilidad. Revisión de calidad de productos. Mantenimiento del estado de formación GMP del personal relevante. Requisitos: Licenciatura en Química, Farmacia, Biología o similar o Ingeniería Química, Técnica o Superior. Experiencia en unidades de calidad de compañías fabricantes de materia prima farmacéutica o producto terminado para farmacia. Buen nivel de inglés.

COMPULSORY TRAINING • Technical or Higher Engineering in branches such as Mechanical, Industrial, Metallurgy or similar., • Complementary training in maintenance management, occupational risk prevention, customer service and quality is highly valued. REQUIRED EXPERIENCE • 5 to 8 years of experience in supervisor positions or head of technical service, maintenance or after-sales in the industrial/metallurgical sector and/or preferably within the mobile elevating personnel platform sector, • Experience in team management and project coordination., • Experience working with ERP systems (SAP, Oracle, Navision, etc.) and service management tools. LANGUAGES • Spanish level C1 in effective competence., • C1 at Catalan level in effective competition., • Minimum English level B2-C1 – Technical English, • French level B1 or higher (recommended). SKILLS & KNOWLEDGE • Organizational and time and resource management skills., • Communication, organization, and planning skills., • Responsible, organized, dynamic and methodical person., • Leadership and ability to motivate teams., • Ability to train and develop talent within the team, • Customer orientation., • Ability to negotiate and resolve conflicts., • Management of maintenance management software and CRM., • Strategic vision and orientation to results. TRAINING TO BE PROVIDED BY THE COMPANY • Epicor software and/or fulfillment software, • Training in occupational risk prevention in the workplace, • Training in labor processes MAIN FUNCTIONS • Supervision, control and management of the personnel in charge: administrative staff and mechanics, • Assignment of tasks and supervision of the same., • Coordination with the documentation administration department for the invoicing of interventions or management of guarantees., • After-sales service management: coordinating customer service, technical support and incident resolution., • Management and planning of customer portfolio, maintenance contracts, repairs and breakdowns., • Telephone and/or personal customer service., • Permit management, current legal regulations to be complied with, etc..., • Development and implementation of new strategies and procedures to ensure efficient and high-quality technical service: monitoring programs, surveys and continuous improvement actions., • Identify areas for improvement and make data-driven decisions to improve team performance and customer satisfaction. For IPAF trainers only: • Management and planning of IPAF courses., • Provide IPAF training and/or courses., • Coordination with the IPAF federation to update regulations, procedures, etc., • Manage IPAF audits.

REQUIRED TRAINING • Intermediate or Higher Degree in Logistics, • Vocational training in mechanical, metallurgical, or logistics disciplines may also be considered and positively valued, • Additional training in inventory management, procurement, or ERP systems is a plus. REQUIRED EXPERIENCE • 3–5 years of experience in spare parts management, purchasing, or inventory control within the metallurgical or industrial sector., • Proven track record in supplier management, demand planning, and stock optimization., • Experience working with ERP systems (SAP, Oracle, Navision, etc.) and warehouse management tools. LANGUAGES • Spanish level C1 in effective competence., • Catalan level C1 in effective competition., • English minimum level B2-C1. SKILLS & KNOWLEDGE • Organizational and time management skills., • Methodical and detail-oriented person., • Communication, organization and planning skills., • Teamwork and collaboration., • Familiarity with modern storage practices and methods., • Mastery of computer programs + Office suite, databases and inventory systems (assessable), • Order and neatness at work, • Responsible, organized, dynamic and methodical person., • Attention in personal treatment TRAINING TO BE PROVIDED BY THE COMPANY • Epicor software and/or logistics management software, • Workplace occupational risk prevention training, • Job Process Training MAIN FUNCTIONS • Spare parts management, • Monitoring, status and maintenance of references in the system., • Buy/Sell Price and Profit Margin Analysis, • Tracking and control of processed and invoiced customer orders, • Reception, storage and processing of warehouse products (picking, unloading, labelling, storing parcels, machinery, etc...), • Perform inventory controls, orders, and maintain a high level of quality for audits, • Check the stock level, complete daily records, and perform goods procurement, • Delivery note management, • Communicate and cooperate with supervisors and co-workers, • Placing orders with suppliers, • Budget Preparation, • Warranty management with internal and external suppliers, • Supply parts and spare parts to workshop

QA Engineer Process Specialist Location: Granollers, Spain Term: 12 Month Fixed Term Contract About the Role The QA Engineer Process Specialist ensures products and processes meet high standards of quality, reliability, and performance in a manufacturing environment focused on cosmetics or food sectors. This hands-on role involves collaborating with R&D and production teams to industrialise new formulas, control manufacturing processes for liquids and solids, and drive continuous improvement. Responsibilities include conducting industrial tests, setting process parameters, analysing manufacturing risks, implementing GMP systems, and managing sanitary measures to prevent contamination. The Ideal Candidate Experience: • University degree in chemical engineering, laboratory sciences, or quality (higher degree preferred)., • Minimum 23 years in similar QA or process engineering roles, ideally in cosmetics or food (non-pharma)., • Proven hands-on factory experience, comfortable navigating production floors daily. Skills & Attributes: • Strong knowledge of hygienic design, equipment types, pumps, and metrology., • Good English level (B2-C1, test required)., • Field-oriented, collaborative, with expertise in GMP, risk analysis, and process optimisation. Key Responsibilities • Collect formulas, perform industrial tests, monitor processes, and set parameters for factory implementation., • Collaborate with R&D and departments to industrialise new formulas and control liquid/solid manufacturing., • Analyse manufacturing risks, ensure GMP compliance, drive continuous improvement, and maintain sanitary facilities for disinfection. Apply Now This role offers a chance to shape quality processes in a dynamic manufacturing setting, leveraging deep expertise to safeguard product standards. Field-experienced QA specialists with strong technical backgrounds in cosmetics or food production are encouraged to apply.

COMPULSORY TRAINING Technical or Higher Engineering in branches such as Mechanical, Industrial, Metallurgy or similar. Complementary training in maintenance management , occupational risk prevention, customer service and quality is highly valued. REQUIRED EXPERIENCE ~5 to 8 years of experience in supervisor positions or head of technical service, maintenance or after-sales in the industrial/metallurgical sector and/or preferably within the mobile elevating personnel platform sector ~ Experience in team management and project coordination. ~ Experience working with ERP systems (SAP, Oracle, Navision, etc.) and service management tools. LANGUAGES Spanish level C1 in effective competence. C1 at Catalan level in effective competition. Minimum English level B2-C1 – Technical English French level B1 or higher (recommended). SKILLS & KNOWLEDGE Organizational and time and resource management skills. Communication, organization, and planning skills. Responsible, organized, dynamic and methodical person. Leadership and ability to motivate teams. Ability to train and develop talent within the team Customer orientation. Ability to negotiate and resolve conflicts. Management of maintenance management software and CRM. Strategic vision and orientation to results. TRAINING TO BE PROVIDED BY THE COMPANY Epicor software and/or fulfillment software Training in occupational risk prevention in the workplace Training in labor processes MAIN FUNCTIONS Supervision, control and management of the personnel in charge: administrative staff and mechanics Assignment of tasks and supervision of the same. Coordination with the documentation administration department for the invoicing of interventions or management of guarantees. After-sales service management: coordinating customer service, technical support and incident resolution. Management and planning of customer portfolio, maintenance contracts, repairs and breakdowns. Telephone and/or personal customer service. Permit management, current legal regulations to be complied with, etc... Development and implementation of new strategies and procedures to ensure efficient and high-quality technical service: monitoring programs, surveys and continuous improvement actions. Identify areas for improvement and make data-driven decisions to improve team performance and customer satisfaction. For IPAF trainers only : Management and planning of IPAF courses. Provide IPAF training and/or courses. Coordination with the IPAF federation to update regulations, procedures, etc. Manage IPAF audits.

COMPULSORY TRAINING Technical or Higher Engineering in branches such as Mechanical, Industrial, Metallurgy or similar. Complementary training in maintenance management , occupational risk prevention, customer service and quality is highly valued. REQUIRED EXPERIENCE ~5 to 8 years of experience in supervisor positions or head of technical service, maintenance or after-sales in the industrial/metallurgical sector and/or preferably within the mobile elevating personnel platform sector ~ Experience in team management and project coordination. ~ Experience working with ERP systems (SAP, Oracle, Navision, etc.) and service management tools. LANGUAGES Spanish level C1 in effective competence. C1 at Catalan level in effective competition. Minimum English level B2-C1 – Technical English French level B1 or higher (recommended). SKILLS & KNOWLEDGE Organizational and time and resource management skills. Communication, organization, and planning skills. Responsible, organized, dynamic and methodical person. Leadership and ability to motivate teams. Ability to train and develop talent within the team Customer orientation. Ability to negotiate and resolve conflicts. Management of maintenance management software and CRM. Strategic vision and orientation to results. TRAINING TO BE PROVIDED BY THE COMPANY Epicor software and/or fulfillment software Training in occupational risk prevention in the workplace Training in labor processes MAIN FUNCTIONS Supervision, control and management of the personnel in charge: administrative staff and mechanics Assignment of tasks and supervision of the same. Coordination with the documentation administration department for the invoicing of interventions or management of guarantees. After-sales service management: coordinating customer service, technical support and incident resolution. Management and planning of customer portfolio, maintenance contracts, repairs and breakdowns. Telephone and/or personal customer service. Permit management, current legal regulations to be complied with, etc... Development and implementation of new strategies and procedures to ensure efficient and high-quality technical service: monitoring programs, surveys and continuous improvement actions. Identify areas for improvement and make data-driven decisions to improve team performance and customer satisfaction. For IPAF trainers only : Management and planning of IPAF courses. Provide IPAF training and/or courses. Coordination with the IPAF federation to update regulations, procedures, etc. Manage IPAF audits.

COMPULSORY TRAINING Technical or Higher Engineering in branches such as Mechanical, Industrial, Metallurgy or similar. Complementary training in maintenance management , occupational risk prevention, customer service and quality is highly valued. REQUIRED EXPERIENCE ~5 to 8 years of experience in supervisor positions or head of technical service, maintenance or after-sales in the industrial/metallurgical sector and/or preferably within the mobile elevating personnel platform sector ~ Experience in team management and project coordination. ~ Experience working with ERP systems (SAP, Oracle, Navision, etc.) and service management tools. LANGUAGES Spanish level C1 in effective competence. C1 at Catalan level in effective competition. Minimum English level B2-C1 – Technical English French level B1 or higher (recommended). SKILLS & KNOWLEDGE Organizational and time and resource management skills. Communication, organization, and planning skills. Responsible, organized, dynamic and methodical person. Leadership and ability to motivate teams. Ability to train and develop talent within the team Customer orientation. Ability to negotiate and resolve conflicts. Management of maintenance management software and CRM. Strategic vision and orientation to results. TRAINING TO BE PROVIDED BY THE COMPANY Epicor software and/or fulfillment software Training in occupational risk prevention in the workplace Training in labor processes MAIN FUNCTIONS Supervision, control and management of the personnel in charge: administrative staff and mechanics Assignment of tasks and supervision of the same. Coordination with the documentation administration department for the invoicing of interventions or management of guarantees. After-sales service management: coordinating customer service, technical support and incident resolution. Management and planning of customer portfolio, maintenance contracts, repairs and breakdowns. Telephone and/or personal customer service. Permit management, current legal regulations to be complied with, etc... Development and implementation of new strategies and procedures to ensure efficient and high-quality technical service: monitoring programs, surveys and continuous improvement actions. Identify areas for improvement and make data-driven decisions to improve team performance and customer satisfaction. For IPAF trainers only : Management and planning of IPAF courses. Provide IPAF training and/or courses. Coordination with the IPAF federation to update regulations, procedures, etc. Manage IPAF audits.

COMPULSORY TRAINING Technical or Higher Engineering in branches such as Mechanical, Industrial, Metallurgy or similar.Complementary training in maintenance management , occupational risk prevention, customer service and quality is highly valued.REQUIRED EXPERIENCE ~5 to 8 years of experience

Colabora en la optimización y mejora de los sistemas de calidad, revisando documentación y realizando auditorías.

Participate in the development and maintenance of quality procedures related to complaints, vigilance system and post-market surveillance. You have 2 years of experience in Quality Assurance within pharmaceutical industry and/or medical devices.

Participate in the development and maintenance of quality procedures related to complaints, vigilance system and post-market surveillance. You have 2 years of experience in Quality Assurance within pharmaceutical industry and/or medical devices.

Buscas un puesto estable? ¿Aportas experiencia en calidad en compañías fabricantes de materia prima farmacéutica o producto terminado para farmacia? ¿Te gustaría trabajar en una importante empresa del sector químico farmacéutico, dedicada al desarrollo y fabricación de principios activos, u

Descripción del puesto El/la Quality Control (QC) será responsable de garantizar que todos los productos y procesos cumplen con los estándares de calidad internos y normativos antes de su liberación.

The QA Engineer Process Specialist ensures products and processes meet high standards of quality, reliability, and performance in a manufacturing environment focused on cosmetics or food sectors. University degree in chemical engineering, laboratory sciences, or quality (higher degree preferred). Th

Recepción y control de materias primas y productos.Ciencias, Farmacia, Biotecnología, Química o similar.Organización, atención al detalle y rigor.Flexibilidad y adaptabilidad a cambios en procedimientos y proyectos.

QA Engineer Process Specialist Location: Granollers, Spain Term: 12 Month Fixed Term Contract About the Role The QA Engineer Process Specialist ensures products and processes meet high standards of quality, reliability, and performance in a manufacturing environment focused on cosmetics or foo

Recepción y control de materias primas y productos.Ciencias, Farmacia, Biotecnología, Química o similar.Organización, atención al detalle y rigor.Flexibilidad y adaptabilidad a cambios en procedimientos y proyectos.

The QA Engineer Process Specialist ensures products and processes meet high standards of quality, reliability, and performance in a manufacturing environment focused on cosmetics or food sectors. University degree in chemical engineering, laboratory sciences, or quality (higher degree preferred). Th

Buscas un puesto estable? ¿Aportas experiencia en calidad en compañías fabricantes de materia prima farmacéutica o producto terminado para farmacia? ¿Te gustaría trabajar en una importante empresa del sector químico farmacéutico, dedicada al desarrollo y fabricación de principios activos, u

Provide feedback concerning the quality of the application. If you're ready to be at the forefront of change, have a passion for Quality, and thrive in an innovative environment, we'd love to hear from you.

Buscas un puesto estable? ¿Aportas experiencia en calidad en compañías fabricantes de materia prima farmacéutica o producto terminado para farmacia? ¿Te gustaría trabajar en una importante empresa del sector químico farmacéutico, dedicada al desarrollo y fabricación de principios activos, u

Descripción del puesto El/la Quality Control (QC) será responsable de garantizar que todos los productos y procesos cumplen con los estándares de calidad internos y normativos antes de su liberación.

Buscas un puesto estable? ¿Aportas experiencia en calidad en compañías fabricantes de materia prima farmacéutica o producto terminado para farmacia? ¿Te gustaría trabajar en una importante empresa del sector químico farmacéutico, dedicada al desarrollo y fabricación de principios activos, u

Recepción y control de materias primas y productos.Ciencias, Farmacia, Biotecnología, Química o similar.Organización, atención al detalle y rigor.Flexibilidad y adaptabilidad a cambios en procedimientos y proyectos.

Buscas un puesto estable? ¿Aportas experiencia en calidad en compañías fabricantes de materia prima farmacéutica o producto terminado para farmacia? ¿Te gustaría trabajar en una importante empresa del sector químico farmacéutico, dedicada al desarrollo y fabricación de principios activos, u

Qué ofrecemos Contrato estable.Funciones principales Control organoléptico.Recepción y control de materias primas y productos.Ciencias, Farmacia, Biotecnología, Química o similar.Experiencia: Experiencia previa en.Conocimientos y habilidades: Conocimiento de.Organización, atención al detalle

Buscas un puesto estable? ¿Aportas experiencia en calidad en compañías fabricantes de materia prima farmacéutica o producto terminado para farmacia? ¿Te gustaría trabajar en una importante empresa del sector químico farmacéutico, dedicada al desarrollo y fabricación de principios activos, u

Maximice sus posibilidades de que su candidatura sea seleccionada asegurándose de que su CV y sus habilidades se ajustan al perfil.Recepción y control de materias primas y productos.Ciencias, Farmacia, Biotecnología, Química o similar.Organización, atención al detalle y rigor.Flexibilidad y ad

Somos la firma global de talento: Selección, headhunting, formación y consultoría de Eurofirms Group.En Claire Joster creemos en el talento único de cada persona y sabemos que la diversidad aporta valor a los equipos, impulsando organizaciones más innovadoras, creativas y eficientes.Por eso, co

Role Responsibilities: Assist Test Engineer to carry out all the test and de-bug related activities Perform hands-on assembly & disassembly of testing equipment/device so that testing activities is in accordance to work instructions, test procedures and work schedule Review and clarify test requirem

Responsibilities: Perform quality control analysis on essential oils and aroma chemicals Carry out chemical tests according to internal specifications and industry standars Conduct organoleptic evaluations (taste and smell analysis) Operate and interpret results using GC-FID and GC-MS instruments P

Quality Controller a l'àrea de Producció. Col·laboració directa amb Quality Manager, enginyeria i producció.

BioSystems diseña, desarrolla, fabrica y comercializa soluciones analíticas, creando tanto pruebas de reactivos como instrumentación analítica para laboratorios de diagnóstico in vitro (IVD), así como para fines industriales.Nuestro objetivo es mejorar la salud y el bienestar en todo el mundo.

Quality & Regulatory Affairs Manager – Sector OTC (Barcelona). Desde LHH Life Sciences estamos seleccionando un/a Quality & Regulatory Affairs Manager para Multinacional líder en sector OTC, ubicada en Barcelona.

Participating in quality assurance projects as writing procedures and work instructions. You’ve gained experience in a pharmaceutical GxP environment (Engineering, Maintenance, Validations, Production, or Quality Assurance). For over 20 years, Rephine has been at the forefront of improving manufac

Empresa industrial referente internacional en su sector en plena fase de expansión precisa incorporar un/a Quality & Environment Manager.

Solutia Life Sciences (división de reclutamiento de Solutia) se especializa en perfiles técnicos y mandos intermedios en los sectores farmacéutico, biotecnológico y de dispositivos médicos.Desde Solutia Life Sciences buscamos un líder apasionado por la calidad y las personas para asumir el rol

We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. Quality Control (QC) Technician – Biologics - Morning Shift 6am-2pm. Design, supervise, and execute qua

Create and standardize quality control and reporting across projects. Act as a point of contact for quality validation, ensuring that final deliverables meet both technical and functional excellence standards. ML project quality assurance, focusing on functional, performance, and automation testing.

Strong command of GMP/GDP regulations and Quality Management Systems. In this role, you will be the primary Quality point of contact for. Act as the Quality Lead for assigned molecules and finished dosage forms (FDFs), overseeing lifecycle changes, API source updates, and manufacturing process optim

A fantastic opportunity for Quality Control Engineer to join fast-growing deep-tech company, who provide hyper-efficient software to global companies across finance, energy, manufacturing and cybersecurity to gain an edge with quantum computing and artificial intelligence. Evaluate system quality un

Quality Controller a l'àrea de Producció. Col·laboració directa amb Quality Manager, enginyeria i producció.

Create and standardize quality control and reporting across projects. Act as a point of contact for quality validation, ensuring that final deliverables meet both technical and functional excellence standards. ML project quality assurance, focusing on functional, performance, and automation testing.

Quality & Regulatory Affairs Manager – Sector OTC (Barcelona). Desde LHH Life Sciences estamos seleccionando un/a Quality & Regulatory Affairs Manager para Multinacional líder en sector OTC, ubicada en Barcelona.

Empresa industrial referente internacional en su sector en plena fase de expansión precisa incorporar un/a Quality & Environment Manager.

Quality Control (QC) Technician – Biologics - Morning Shift 6am-2pm. Design, supervise, and execute quality control studies for biological products, with a strong focus on. Provide direction and supervision to technical staff, ensuring high-quality experimental execution and compliance with regula

As a member of the Quality Department, you will collaborate closely with all teams and departments at Mediktor, supporting them in meeting regulatory and quality requirements. Participate in internal and external audits to verify adherence to quality standards. Partner with teams to integrate and up