Quality jobs in TorderaCreate job alerts

Are you passionate about fashion, sports and an active lifestyle? In OYSHO, we are looking for a talented Fashion Buyer to join our Activewear department. Our location is in Tordera, (Barcelona) from where you will be able to design collections and set the trends on sportswear for all our stores worlwide. Oysho is a sport and leisure brand committed to innovation, quality and sustainability. We offer a broad range of technical collections designed to deliver peak athletic performance and maximum comfort. Your main functions would be: • To analyse the previous year’s sales and the season’s key trends in order to identify the principal sales requirements., • To work with the design team on the inicial and final product selection, taking into consideration factors such as time, the season’s key trends and sales requirements in accordance with the previous year’s sales., • To define the final buying structure once the product has been selected and the budget has been sent by the management control department for the family and sub-family buying., • To maintain a strong working relationship with suppliers to ensure a co-operative approach is maintained at all times and negotiate best terms (prices and delivery dates)., • To monitor production to ensure compliance with the agreed terms and conditions., • To carry out the sample fittings with the pattern/quality and design teams and to provide the suppliers with feedback in order to adjust and improve the samples., • To maintain a strong awareness of market trends and competitor activity in order to ensure uniqueness and newness on approach to Buying. How do we imagine you? To be successful in this position, you must have a positive attitude, with the ability to adapt quickly in a dynamic environment. Furthermore, you must be able to demonstrate: • Between 3 and 4 years of experience (similar post or retail sector)., • That you have an analytical profile, with negotiation skills and sensitivity for fashion and the product (fabrics, qualities, patterns)., • Higher education qualification in Economics, Business Administration and Management or Business Studies., • High level of English and Spanish. What do you get? Working at Oysho is joining a team where creativity and innovation are our DNA. • The sky is the limit 🚀 : our inner talent is our greatest advantage. You'll have a world of opportunities to grow, learn, and make a difference., • Always Learning: Through TRAIN, our e-learning platform, you will be able to access different training courses, talks and content that will allow you to grow and develop., • International atmosphere: more than 15 nationalities working with you. Real diversity on a day-to-day basis., • Wellbeing: Improve your wellbeing with a variety of services designed to take care of you, from subsidized canteen service with km0 food to medical services and physiotherapy. 🍏, • Easy Move: 🚌 transport from key points in Barcelona, Mataró and Vallès, or parking with chargers for your electric car., • Fit & Fun: gym and directed classes to maintain a balance body and mind., • Fashion for You: enjoy a 25% discount on all our brands., • Relocation: We help you in your move, both nationally and internationally, so that your adaptation is as comfortable as possible. IT'S YOUR TIME! "If you want to take the next step in your career, work in a dynamic environment and bring quality to our collections, this is your place." We are waiting for you!

About Us: As a global life science company, taking care of human, animal and plant life has been our priority for 50 years. Today, we are a world leader in the production of heparin – the primary anticoagulant used to save approximately 100 million lives every year. We have also set the benchmark for the manufacture of APIs and functional ingredients for the pharmaceutical, nutraceutical, veterinary, animal nutrition and agricultural sectors. We work to innovate in human, animal, and plant health. We believe that partnership is the key to success and we support our partners across the healthcare, plant and animal health markets worldwide. About the Role: • Take responsibility for managing the Industrial Manufacturing Control and Instrumentation System, both hardware and software, to ensure proper operation in accordance with corporate safety, quality and environmental standards., • Lead the implementation of the industrial manufacturing control system and take responsibility for its updating and supervision., • Motivate, drive and support change management in new programmes and practices, organisational behaviour, as well as technical solutions related to the processes under your responsibility., • Be responsible for the implementation and continuous improvement of your processes to strengthen the organisation's integrated management system for safety, quality, environment and sustainability., • Take responsibility for the department and manage the process of establishing the main directions and priorities in order to meet tight production deadlines and maintain plant availability, ensuring high levels of safety and quality as required., • Take responsibility for ensuring that engineering and maintenance activities are carried out in a timely manner and within budget, take an active role in obtaining supply contracts and, therefore, in controlling the budget., • Ensure that the organisation is at the forefront of new technologies in operational management. Ensure that Bioibérica's control and instrumentation facilities are state of the art. Responsibilities: • Ensure that all current safety, quality and environmental standards are applied in all activities carried out and ensure that other Bioibérica colleagues, internal and external suppliers involved in these activities also comply with them., • Manage the design, configuration and programming of the automated control system using SCADA Aveva System Platform or Intouch and Rockwell or Siemens PLCs., • Develop and implement control strategies to ensure the efficiency and safety of processes in the pharmaceutical industry., • Manage the integration of SCADA and PLC systems to enable effective communication and precise control of the equipment and processes involved in production., • Oversee the testing and commissioning of automation systems, ensuring their correct operation and compliance with quality, safety and environmental requirements., • Ensure that technical documentation is up to date, including control diagrams, user manuals, and validation procedures., • Comply with pharmaceutical industry standards and regulations, such as Good Manufacturing Practices (GMP) and system validation requirements (GAMP 5 and 21 CFR Part 11)., • Provide technical support and training to end users of automation systems., • Keep your knowledge up to date, both technically and legally, on issues related to GMPs, the environment, quality, occupational risk prevention, and industrial safety., • Maintain order and cleanliness in your workplace and in all areas where you carry out your activities. About You: • Experience working in the pharmaceutical environment and knowledge of the pharmaceutical and chemical business, manufacturing and quality processes (GxP compliance, validation and quality systems management, GMP Annex 11, 21CFR Part 11)., • University degree in Electrical Engineering, Electronic Engineering, Automation Engineering or related field, or CFGM/CFGS in Electrical Engineering., • Desirable: Aveva System Platform, Intouch Wonderware What’s Next: If this sounds like a role that you would be interested in, then we would love to hear from you. Apply with a copy of your CV at the link below. *Please apply with your CV in English where possible We value the support recruitment agencies provide, however we are unable to accept speculative CV’s from agencies we are not already engaged with. Closing Date: 5th January 2026 *Please note, closing dates are subject to change and, at time of high volume of applications, this may be brought forward. Other important information: Equality and diversity at Bioiberica: We value diversity and are committed to an inclusive working environment in which all employees are respected and supported regardless of gender, age, ethnic origin, religion, sexual orientation, disability, or social background. We expressly welcome applications from people with a wide range of perspectives and experiences. Our goal is to ensure equal opportunities and actively combat discrimination – both in the application process and in everyday working life.

About Us: As a global life science company, taking care of human, animal and plant life has been our priority for 50 years. Today, we are a world leader in the production of heparin – the primary anticoagulant used to save approximately 100 million lives every year. We have also set the benchmark for the manufacture of APIs and functional ingredients for the pharmaceutical, nutraceutical, veterinary, animal nutrition and agricultural sectors. We work to innovate in human, animal, and plant health. We believe that partnership is the key to success and we support our partners across the healthcare, plant and animal health markets worldwide. About the Role: The role will involve resolution of production problems, process optimisation and commissioning of new industrial facilities for the Group. Collaboration with Quality, Safety and Environment in the continuous auditing of processes based on technical knowledge of processes and facilities. Responsibilities: • Carry out operations related to the transfer and optimisation of industrial processes at Bioiberica's national and international plants, ensuring regulatory compliance by recording and evaluating the associated change control., • Collaborate in the preparation of reports derived from the evaluation of change requests, deviations and nonconformities affecting products, processes or equipment., • Collaborate with Engineering in defining user requirements for new production facilities and equipment., • Collaborate in reviewing the specifications of MMPPs, materials, in-process controls, intermediates and APIs produced, ensuring that their content corresponds to the DMF., • Collaborate as a member of the HACCP team in the identification, evaluation and control of significant hazards, ensuring compliance with current food safety regulations., • Participate in the verification and validation of the HACCP plan, ensuring the effectiveness of preventive and corrective measures., • Prepare manufacturing guidelines for new processes or optimisation of existing ones, as well as validation of processes prior to their industrial implementation., • Resolving production problems that require different solutions, collaborating in the monitoring of process optimisation projects, collaborating in the feasibility study of alternative MMPPs, collaborating with other areas of the company at a technical advisory level (commercial, customer service, RRAA)., • Possibility of participating in cross-functional projects that the company, based on your strengths and skills, may consider appropriate for you to participate in. About You: • A degree in Chemistry or Life Sciences, • Strong communication skills, • Fluent in English & Spanish What’s Next: If this sounds like a role that you would be interested in, then we would love to hear from you. Apply with a copy of your CV at the link below. *Please apply with your CV in English where possible We value the support recruitment agencies provide, however we are unable to accept speculative CV’s from agencies we are not already engaged with. Closing Date: 5th January 2026 *Please note, closing dates are subject to change and, at time of high volume of applications, this may be brought forward. Other important information: Equality and diversity at Bioiberica: We value diversity and are committed to an inclusive working environment in which all employees are respected and supported regardless of gender, age, ethnic origin, religion, sexual orientation, disability, or social background. We expressly welcome applications from people with a wide range of perspectives and experiences. Our goal is to ensure equal opportunities and actively combat discrimination – both in the application process and in everyday working life.

About Us: As a global life science company, taking care of human, animal and plant life has been our priority for 50 years. Today, we are a world leader in the production of heparin – the primary anticoagulant used to save approximately 100 million lives every year. We have also set the benchmark for the manufacture of APIs and functional ingredients for the pharmaceutical, nutraceutical, veterinary, animal nutrition and agricultural sectors. We work to innovate in human, animal, and plant health. We believe that partnership is the key to success and we support our partners across the healthcare, plant and animal health markets worldwide. About the Role: Ensure regulatory compliance and quality in GMP processes, acting as QA and Compliance Manager and as backup for the API QA Technician. Ensure document traceability, correct management of deviations, CAPAs and changes, and provide support in audits, Regulatory Affairs and document release, minimising regulatory risks and ensuring compliance with international standards. Responsibilities: Review of GMP documentation (API technical backup): • Review and approve production spreadsheets, records and controls in accordance with GMP and PNT., • Verify the integrity, traceability and accuracy of critical data (processes, in-process controls, times, equipment)., • Coordinate the investigation, closure and verification of deviations and non-conformities., • Supervise the investigation of OOS/OOT, ensuring immediate action, root cause analysis and action plan., • Prepare, review and control versions of SOPs, technical instructions, spreadsheets and GMP forms., • Keep the document management system up to date in accordance with ICH Q7 and applicable regulations., • Participate in customer complaint investigations, ensuring feedback to the quality system., • Coordinate the change management process on the MasterControl platform., • Prepare and maintain documentation to be provided by QA for regulatory dossiers, site master files, certificates and documentation for authorities., • Ensure compliance with legal requirements for labelling and records., • Provide support in regulatory audits and inspections (EMA, FDA, AEMPS)., • Collaborate in the evaluation and approval of raw materials, critical services and auxiliary materials., • Participate in internal, customer and authority audits., • Prepare evidence, records and corrective action plans., • Prepare APR/PQR reports and management reviews., • Participate in continuous improvement projects., • Be the point of contact for customer enquiries and approvals., • Provide GMP training during onboarding and periodic training sessions., • Be familiar with and apply current regulations on safety, health, occupational risk prevention, quality, the environment and energy efficiency, and ensure compliance with them., • Report any risk situation in accordance with incident/accident management and quality event management procedures. About You: • Degree in Pharmacy, Chemistry, Biotechnology or similar., • Solid knowledge of GMP, ICH Q7, ISO and applicable regulations., • Training in Compliance and Regulatory Affairs is desirable., • Internal Auditor certification in GMP, GLP, GDP, Quality Management Systems (food, feed) is desirable., • Minimum 2 years in QA and Compliance in GMP environments (pharmaceutical, API, chemical)., • Experience in document management, audits, deviations and CAPAs., • Experience in Regulatory Affairs and supplier management is desirable., • Knowledge of the EU, FDA and EAEU regulatory environment and specific international regulations in destination countries. What’s Next: If this sounds like a role that you would be interested in, then we would love to hear from you. Apply with a copy of your CV at the link below. *Please apply with your CV to in English where possible We value the support recruitment agencies provide, however we are unable to accept speculative CV’s from agencies we are not already engaged with. Closing Date: 5th January 2026 *Please note, closing dates are subject to change and, at time of high volume of applications, this may be brought forward. Other important information: Equality and diversity at Bioiberica: We value diversity and are committed to an inclusive working environment in which all employees are respected and supported regardless of gender, age, ethnic origin, religion, sexual orientation, disability, or social background. We expressly welcome applications from people with a wide range of perspectives and experiences. Our goal is to ensure equal opportunities and actively combat discrimination – both in the application process and in everyday working life.

Are you passionate about fashion, sports and an active lifestyle? In OYSHO, we are looking for a talented Senior Designer to join our Activewear Department. Our location is in Tordera, (Barcelona) from where you will be able to design collections and set the trends on sportswear for all our stores worlwide. Oysho is a sport and leisure brand committed to innovation, quality and sustainability. We offer a broad range of technical collections designed to deliver peak athletic performance and maximum comfort. Your main functions would be: • Interpreting concept & researching trends in favor of main collection assuring the visibility of OYSHO DNA in each garment., • Solid understanding of fabrics, details, trims, fit and construction., • Work closely with other members of Activewear team on creating and developing new collections, garments, concepts and patterns from brainstorming the ideas to the final product., • Draw the technical files for our suppliers to ensure that quality, construction, and fit are aligned with brand needs. How do we imagine you? To be successful in this position, you must have a positive attitude, with the ability to adapt quickly in a dynamic environment. Furthermore, you must be able to demonstrate: • 5+ years of professional experience in a similar position in an international environment., • Be aware of trends, brands, designers, catwalks: be a passionate fashion and sports lover., • Excellent communication skills with the ability to adapt to a fast-paced ever-changing environment., • The ability to demonstrate outstanding creative instincts and a distinct point of view., • Very good/ fluent knowledge of English. What do you get? Working at Oysho is joining a team where creativity and innovation are our DNA. • The sky is the limit 🚀 : our inner talent is our greatest advantage. You'll have a world of opportunities to grow, learn, and make a difference., • Always Learning: Through TRAIN, our e-learning platform, you will be able to access different training courses, talks and content that will allow you to grow and develop., • International atmosphere: more than 15 nationalities working with you. Real diversity on a day-to-day basis., • Wellbeing: Improve your wellbeing with a variety of services designed to take care of you, from subsidized canteen service with km0 food to medical services and physiotherapy. 🍏, • Easy Move: 🚌 transport from key points in Barcelona, Mataró and Vallès, or parking with chargers for your electric car., • Fit & Fun: gym and directed classes to maintain a balance body and mind., • Fashion for You: enjoy a 25% discount on all our brands., • Relocation: We help you in your move, both nationally and internationally, so that your adaptation is as comfortable as possible. IT'S YOUR TIME! "If you want to take the next step in your career, work in a dynamic environment and bring quality to our collections, this is your place." We are waiting for you!

About Us: As a global life science company, taking care of human, animal and plant life has been our priority for 50 years. Today, we are a world leader in the production of heparin – the primary anticoagulant used to save approximately 100 million lives every year. We have also set the benchmark for the manufacture of APIs and functional ingredients for the pharmaceutical, nutraceutical, veterinary, animal nutrition and agricultural sectors. We work to innovate in human, animal, and plant health. We believe that partnership is the key to success and we support our partners across the healthcare, plant and animal health markets worldwide. About the Role: Ensure the proper administrative management of the Quality Assurance (QA) area, ensuring compliance with GMP requirements and applicable regulations, through the organisation, control and archiving of critical documentation, support in audits and coordination with other areas. Responsibilities: Document management and record control: • Create, review and update Standard Operating Procedures (SOPs)., • Control versions and ensure the correct distribution of current documents., • File physical and digital documentation in compliance with traceability requirements., • Record quality events in the system., • Follow up on actions arising from events (AI) and ensure compliance with deadlines., • Prepare periodic reports on quality indicators., • Monitor the release status of batches to ensure on-time deliveries to customers., • Coordinate with Production, Logistics and Customer Service to ensure availability., • Act as the QA liaison with the areas involved in order tracking., • Manage QA team schedules and meetings., • Prepare minutes and reports of quality-related meetings., • Maintain staff training records in the document management system (MasterControl)., • Coordinate the scheduling of courses and internal assessments related to the Quality area (GMP/HACCP/HALAL/GMP+, etc.)., • Prepare documentation required by authorities and auditors., • Organise evidence and records to facilitate review., • Know and apply current standards for safety, health, occupational risk prevention, quality, environment, energy efficiency, and ensure compliance., • Degree in Pharmacy, Chemistry, Biotechnology or similar., • Solid knowledge of GMP regulations and quality management systems., • Additional training in document management and compliance is desirable. What’s Next: If this sounds like a role that you would be interested in, then we would love to hear from you. Apply with a copy of your CV at the link below. *Please apply with your CV to in English where possible We value the support recruitment agencies provide, however we are unable to accept speculative CV’s from agencies we are not already engaged with. Closing Date: 5th January 2026 *Please note, closing dates are subject to change and, at time of high volume of applications, this may be brought forward. Other important information: Equality and diversity at Bioiberica: We value diversity and are committed to an inclusive working environment in which all employees are respected and supported regardless of gender, age, ethnic origin, religion, sexual orientation, disability, or social background. We expressly welcome applications from people with a wide range of perspectives and experiences. Our goal is to ensure equal opportunities and actively combat discrimination – both in the application process and in everyday working life.

Are you a dynamic, creative, and passionate fashion lover ready to take your first step in the industry? If you’re eager to learn, excited about design, and want to experience the fast-paced world of retail, this is your perfect opportunity to kickstart your career with Oysho! We are looking for a Junior Assistant Designer to join our Knitwear Department in Tordera (Barcelona), where you’ll contribute to shaping our global sportswear collections and setting new trends for stores worldwide. This position is part of the Oysho Talent Program, a one-year opportunity designed for recent graduates to gain hands-on experience in one of our key creative areas. Main Responsibilities • Assist in trend research and runway analysis to identify emerging styles and market opportunities., • Support in sourcing and developing new fabrics and materials, helping drive innovation and sustainability., • Create and maintain technical sheets to support the production process and communication with suppliers., • Follow up on sample development, ensuring design accuracy, fit, and quality standards. About You To thrive in this role, you should bring energy, curiosity, and a strong sense of style. You are: • A recent graduate (within the past 3 years) in Fashion Design or a related field., • Passionate about fashion, sports, and trends, with strong awareness of brands, designers, and catwalks., • A team player with strong communication skills and fluency in English (other languages are a plus)., • Creative, detail-oriented, and eager to grow in a dynamic, international environment. What do you get? Working at Oysho is joining a team where creativity and innovation are our DNA. • The sky is the limit 🚀 : our inner talent is our greatest advantage. You'll have a world of opportunities to grow, learn, and make a difference., • Always Learning: Through TRAIN, our e-learning platform, you will be able to access different training courses, talks and content that will allow you to grow and develop., • International atmosphere: more than 15 nationalities working with you. Real diversity on a day-to-day basis., • Wellbeing: Improve your wellbeing with a variety of services designed to take care of you, from subsidized canteen service with km0 food to medical services and physiotherapy. 🍏, • Easy Move: 🚌 transport from key points in Barcelona, Mataró and Vallès, or parking with chargers for your electric car., • Fit & Fun: gym and directed classes to maintain a balance body and mind., • Fashion for You: enjoy a 25% discount on all our brands., • Relocation: We help you in your move, both nationally and internationally, so that your adaptation is as comfortable as possible. IT'S YOUR TIME! "If you want to take the next step in your career, work in a dynamic environment and bring quality to our collections, this is your place." We are waiting for you!

Are you a dynamic, creative, and passionate fashion lover ready to take your first step in the industry? If you’re eager to learn, excited about design, and want to experience the fast-paced world of retail, this is your perfect opportunity to kickstart your career with Oysho ! We are looking for a Junior Assistant Designer to join our Knitwear Department in Tordera (Barcelona), where you’ll contribute to shaping our global sportswear collections and setting new trends for stores worldwide. This position is part of the Oysho Talent Program , a one-year opportunity designed for recent graduates to gain hands-on experience in one of our key creative areas. Main Responsibilities Assist in trend research and runway analysis to identify emerging styles and market opportunities. Support in sourcing and developing new fabrics and materials , helping drive innovation and sustainability. Create and maintain technical sheets to support the production process and communication with suppliers. Follow up on sample development , ensuring design accuracy, fit, and quality standards. About You To thrive in this role, you should bring energy, curiosity, and a strong sense of style. You are: A recent graduate (within the past 3 years) in Fashion Design or a related field. Passionate about fashion, sports, and trends , with strong awareness of brands, designers, and catwalks. A team player with strong communication skills and fluency in English (other languages are a plus). Creative, detail-oriented, and eager to grow in a dynamic, international environment. What do you get? Working at Oysho is joining a team where creativity and innovation are our DNA. ~ The sky is the limit

As a global life science company, taking care of human, animal and plant life has been our priority for 50 years. Today, we are a world leader in the production of heparin – the primary anticoagulant used to save approximately 100 million lives every year. We have also set the benchmark for the manufacture of APIs and functional ingredients for the pharmaceutical, nutraceutical, veterinary, animal nutrition and agricultural sectors. We work to innovate in human, animal, and plant health. We believe that partnership is the key to success and we support our partners across the healthcare, plant and animal health markets worldwide. Ensure regulatory compliance and quality in GMP processes, acting as QA and Compliance Manager and as backup for the API QA Technician. Review and approve production spreadsheets, records and controls in accordance with GMP and PNT. Verify the integrity, traceability and accuracy of critical data (processes, in-process controls, times, equipment). Supervise the investigation of OOS/OOT, ensuring immediate action, root cause analysis and action plan. Document management system and quality assurance (API technical backup): Prepare, review and control versions of SOPs, technical instructions, spreadsheets and GMP forms. Participate in customer complaint investigations, ensuring feedback to the quality system. Develop and control quality indicators and participate in management reviews. Assess potential impacts on quality and safety, validate regulatory compliance, and document execution and closure. Prepare and maintain documentation to be provided by QA for regulatory dossiers, site master files, certificates and documentation for authorities. Ensure compliance with legal requirements for labelling and records. Maintain up-to-date records of supplier approval and monitoring. Quality management system monitoring: Participate in continuous improvement projects. Coordinate with purchasing and the QA Supplier Manager to ensure supply reliability. Quality training and culture: Provide GMP training during onboarding and periodic training sessions. Promote a culture of quality through awareness-raising activities. Be familiar with and apply current regulations on safety, health, occupational risk prevention, quality, the environment and energy efficiency, and ensure compliance with them. Report any risk situation in accordance with incident/accident management and quality event management procedures. Training in Compliance and Regulatory Affairs is desirable. Internal Auditor certification in GMP, GLP, GDP, Quality Management Systems (food, feed) is desirable. Minimum 2 years in QA and Compliance in GMP environments (pharmaceutical, API, chemical). com in English where possible We value diversity and are committed to an inclusive working environment in which all employees are respected and supported regardless of gender, age, ethnic origin, religion, sexual orientation, disability, or social background.

As a global life science company, taking care of human, animal and plant life has been our priority for 50 years. Today, we are a world leader in the production of heparin – the primary anticoagulant used to save approximately 100 million lives every year. We have also set the benchmark for the manufacture of APIs and functional ingredients for the pharmaceutical, nutraceutical, veterinary, animal nutrition and agricultural sectors. We work to innovate in human, animal, and plant health. We believe that partnership is the key to success and we support our partners across the healthcare, plant and animal health markets worldwide. Ensure regulatory compliance and quality in GMP processes, acting as QA and Compliance Manager and as backup for the API QA Technician. Review and approve production spreadsheets, records and controls in accordance with GMP and PNT. Verify the integrity, traceability and accuracy of critical data (processes, in-process controls, times, equipment). Supervise the investigation of OOS/OOT, ensuring immediate action, root cause analysis and action plan. Document management system and quality assurance (API technical backup): Prepare, review and control versions of SOPs, technical instructions, spreadsheets and GMP forms. Participate in customer complaint investigations, ensuring feedback to the quality system. Develop and control quality indicators and participate in management reviews. Assess potential impacts on quality and safety, validate regulatory compliance, and document execution and closure. Prepare and maintain documentation to be provided by QA for regulatory dossiers, site master files, certificates and documentation for authorities. Ensure compliance with legal requirements for labelling and records. Maintain up-to-date records of supplier approval and monitoring. Quality management system monitoring: Participate in continuous improvement projects. Coordinate with purchasing and the QA Supplier Manager to ensure supply reliability. Quality training and culture: Provide GMP training during onboarding and periodic training sessions. Promote a culture of quality through awareness-raising activities. Be familiar with and apply current regulations on safety, health, occupational risk prevention, quality, the environment and energy efficiency, and ensure compliance with them. Report any risk situation in accordance with incident/accident management and quality event management procedures. Training in Compliance and Regulatory Affairs is desirable. Internal Auditor certification in GMP, GLP, GDP, Quality Management Systems (food, feed) is desirable. Minimum 2 years in QA and Compliance in GMP environments (pharmaceutical, API, chemical). com in English where possible We value diversity and are committed to an inclusive working environment in which all employees are respected and supported regardless of gender, age, ethnic origin, religion, sexual orientation, disability, or social background.

As a global life science company, taking care of human, animal and plant life has been our priority for 50 years. Today, we are a world leader in the production of heparin – the primary anticoagulant used to save approximately 100 million lives every year. We have also set the benchmark for the manufacture of APIs and functional ingredients for the pharmaceutical, nutraceutical, veterinary, animal nutrition and agricultural sectors. We work to innovate in human, animal, and plant health. We believe that partnership is the key to success and we support our partners across the healthcare, plant and animal health markets worldwide. Ensure regulatory compliance and quality in GMP processes, acting as QA and Compliance Manager and as backup for the API QA Technician. Review and approve production spreadsheets, records and controls in accordance with GMP and PNT. Verify the integrity, traceability and accuracy of critical data (processes, in-process controls, times, equipment). Supervise the investigation of OOS/OOT, ensuring immediate action, root cause analysis and action plan. Document management system and quality assurance (API technical backup): Prepare, review and control versions of SOPs, technical instructions, spreadsheets and GMP forms. Participate in customer complaint investigations, ensuring feedback to the quality system. Develop and control quality indicators and participate in management reviews. Assess potential impacts on quality and safety, validate regulatory compliance, and document execution and closure. Prepare and maintain documentation to be provided by QA for regulatory dossiers, site master files, certificates and documentation for authorities. Ensure compliance with legal requirements for labelling and records. Maintain up-to-date records of supplier approval and monitoring. Quality management system monitoring: Participate in continuous improvement projects. Coordinate with purchasing and the QA Supplier Manager to ensure supply reliability. Quality training and culture: Provide GMP training during onboarding and periodic training sessions. Promote a culture of quality through awareness-raising activities. Be familiar with and apply current regulations on safety, health, occupational risk prevention, quality, the environment and energy efficiency, and ensure compliance with them. Report any risk situation in accordance with incident/accident management and quality event management procedures. Training in Compliance and Regulatory Affairs is desirable. Internal Auditor certification in GMP, GLP, GDP, Quality Management Systems (food, feed) is desirable. Minimum 2 years in QA and Compliance in GMP environments (pharmaceutical, API, chemical). com in English where possible We value diversity and are committed to an inclusive working environment in which all employees are respected and supported regardless of gender, age, ethnic origin, religion, sexual orientation, disability, or social background.

As a global life science company, taking care of human, animal and plant life has been our priority for 50 years. Today, we are a world leader in the production of heparin – the primary anticoagulant used to save approximately 100 million lives every year. We have also set the benchmark for the manufacture of APIs and functional ingredients for the pharmaceutical, nutraceutical, veterinary, animal nutrition and agricultural sectors. We work to innovate in human, animal, and plant health. We believe that partnership is the key to success and we support our partners across the healthcare, plant and animal health markets worldwide. Ensure regulatory compliance and quality in GMP processes, acting as QA and Compliance Manager and as backup for the API QA Technician. Review and approve production spreadsheets, records and controls in accordance with GMP and PNT. Verify the integrity, traceability and accuracy of critical data (processes, in-process controls, times, equipment). Supervise the investigation of OOS/OOT, ensuring immediate action, root cause analysis and action plan. Document management system and quality assurance (API technical backup): Prepare, review and control versions of SOPs, technical instructions, spreadsheets and GMP forms. Participate in customer complaint investigations, ensuring feedback to the quality system. Develop and control quality indicators and participate in management reviews. Assess potential impacts on quality and safety, validate regulatory compliance, and document execution and closure. Prepare and maintain documentation to be provided by QA for regulatory dossiers, site master files, certificates and documentation for authorities. Ensure compliance with legal requirements for labelling and records. Maintain up-to-date records of supplier approval and monitoring. Quality management system monitoring: Participate in continuous improvement projects. Coordinate with purchasing and the QA Supplier Manager to ensure supply reliability. Quality training and culture: Provide GMP training during onboarding and periodic training sessions. Promote a culture of quality through awareness-raising activities. Be familiar with and apply current regulations on safety, health, occupational risk prevention, quality, the environment and energy efficiency, and ensure compliance with them. Report any risk situation in accordance with incident/accident management and quality event management procedures. Training in Compliance and Regulatory Affairs is desirable. Internal Auditor certification in GMP, GLP, GDP, Quality Management Systems (food, feed) is desirable. Minimum 2 years in QA and Compliance in GMP environments (pharmaceutical, API, chemical). com in English where possible We value diversity and are committed to an inclusive working environment in which all employees are respected and supported regardless of gender, age, ethnic origin, religion, sexual orientation, disability, or social background.

Des de Quality Temporal, estamos buscando personal para importante empresa del sector téxtil ubicado en Massanes.El trabajo consiste en lo siguiente:.Extraer piezas de la maquina y colocarlas en jaulas.Uso de la maquinaria adhesiva y laminado (.Tratamiento y acabado de diferentes tejidos de telas.R

Be familiar with and apply current regulations on safety, health, occupational risk prevention, quality, the environment and energy efficiency, and ensure compliance with them. Internal Auditor certification in GMP, GLP, GDP, Quality Management Systems (food, feed) is desirable. Equality and diversi

Junior Quality Engineer/Quality Technician". Support supplier quality management, including audits, evaluations, and establishing quality agreements. Develop, implement, and maintain quality control processes for manufacturing and maintaining machines.

Report any risk situation in accordance with incident/accident management and quality event management procedures. Equality and diversity at Bioiberica:. Document management system and quality assurance (API technical backup):.

Scientist for Biologics Quality Control. The design, supervision and execution of quality control studies of Biological Products including. Knowlegde of electrophoretic techniques, Western-Blot and ELISAs and Quality Control of Proteins will be a plus.

Prepare minutes and reports of quality-related meetings. Communicate any risk situation in accordance with incident/accident management and quality event management procedures. Equality and diversity at Bioiberica:.

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

Be familiar with and apply current regulations on safety, health, occupational risk prevention, quality, the environment and energy efficiency, and ensure compliance with them. Report any risk situation in accordance with incident/accident management and quality event management procedures. Internal

Experiencia en QA, Quality Systems o QA Operations dentro del sector farma. Conocimientos sólidos en GMP y manejo de Quality Events (deviations, CAPAs, CCs). ALTENSpain #LifeSciences #QualityAssurance #GMP #QAJobs #Pharma.

Quality management system monitoring: Participate in continuous improvement projects. Quality training and culture: Provide GMP training during onboarding and periodic training sessions. Document management system and quality assurance (API technical backup): Prepare, review and control versions of

In this role, you’ll be pivotal in ensuring compliance with Good Manufacturing Practices (GMP) through the validation of facilities, equipment, and processes as well as through the preparation of Quality Systems. Participating in quality assurance projects as writing procedures and work instructio

Support in quality processes: Record quality events in the system. Prepare periodic reports on quality indicators. Prepare minutes and reports of quality-related meetings.

Furthermore, you are part of the EMEA Quality Assurance and Regulatory affairs team, for this region you will be responsible for collecting clinical data from surgeons to assist the HQ in the US with clinical surveillance. In this role you will report directly to the Sr Director Quality Assurance an

Promote a culture of quality through awareness-raising activities. Be familiar with and apply current regulations on safety, health, occupational risk prevention, quality, the environment and energy efficiency, and ensure compliance with them. Report any risk situation in accordance with incident/ac

Girona | 🔄 Contrato 1 año | 🧬 Sector Farmacéutico.Grupo Synergie, estamos colaborando con una organización del sector farmacéutico y biotecnológico, ubicada en el área de Girona, en la búsqueda de un/a.Si te motiva trabajar en un entorno.Formarás parte del equipo de Calidad, dando sopo

Assess potential impacts on quality and safety, validate regulatory compliance, and document execution and closure. Quality management system monitoring: Prepare APR/PQR reports and management reviews. Promote a culture of quality through awareness-raising activities.

Scientist for Biologics Quality Control. The design, supervision and execution of quality control studies of Biological Products including. Knowlegde of electrophoretic techniques, Western-Blot and ELISAs and Quality Control of Proteins will be a plus.

Develop and control quality indicators and participate in management reviews. Assess potential impacts on quality and safety, validate regulatory compliance, and document execution and closure. Promote a culture of quality through awareness-raising activities.

Quality Control Engineer (AI & LLM Services). 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 artif

Asegurar el cumplimiento de requisitos GxP y estándares de Quality Compliance. Experiencia en QA, Quality Systems o QA Operations dentro del sector farma. Conocimientos sólidos en GMP y manejo de Quality Events (deviations, CAPAs, CCs).

Document management system and quality assurance (API technical backup):- Prepare, review and control versions of SOPs, technical instructions, spreadsheets and GMP forms. Participate in customer complaint investigations, ensuring feedback to the quality system. Develop and control quality indicator

Junior Quality Engineer/Quality Technician". Support supplier quality management, including audits, evaluations, and establishing quality agreements. Quality Engineer will work from Barcelona, Spain.

Ensure quality and compliance in GMP processes, managing deviations, CAPAs, and supporting audits in a pharmaceutical environment.

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.

A Quantum Computing & AI software company based in Zaragoza are seeking to bolster their team with a Quality Control engineer. Assess system quality across diverse operating conditions, validating scalability, latency, and data integrity against project expectations. Develop standardized quality-con

Measurement and reporting of Quality KPIs and metrics for the manufacturing area of responsibility. Perform Quality Training to all personnel at Biokit. Standards: Knowledge of Quality standards.

As our Quality Control Engineer, you will be the critical guardian of quality for our high-performance, AI-driven solutions and LLM services. As a Quality Control Engineer, you will:. Evaluate system quality for scalability, latency, and data integrity.

In this role, you’ll be pivotal in ensuring compliance with Good Manufacturing Practices (GMP) through the validation of facilities, equipment, and processes as well as through the preparation of Quality Systems. Participating in quality assurance projects as writing procedures and work instructio

Guarantee the quality and operational reliability of AI solutions across multiple deployments. Establish and standardize quality control processes and reporting across all projects. Serve as a key point of contact for quality validation, ensuring final deliverables meet the highest technical and fun

Ready to lead quality at the infrastructure level of travel?.

This person will foster an organizational culture where quality is a shared value, anticipating risks and generating a positive impact, and will integrate the quality strategy with sustainability to reinforce our position as a benchmark in health, nutrition, and trust. Quality & Food Safety Director

Monitor and report on Quality Management System performance and support quality risk assessments. Continuously assess CDMO/service provider processes and recommend quality and operational improvements. Negotiate and manage Quality Agreements with Suppliers, CDMOs, and other third parties.

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

Buscas una oportunidad estable con potencial de crecimiento en la industria de la automoción?.Nos encantaría conocerte y contarte nuestro proyecto!.Somos una empresa especializada en la fabricación de componentes para vehículos eléctricos, híbridos y de combustión interna.En esta posición, l

As a quality engineer, you will be responsible for achieving quality & productivity performance targets while fostering a customer-focused quality culture. Are you a quality engineer, looking for your next role in Barcelona? We have an excellent opportunity for our client, an engineering manufacture

This position oversees the Quality Control, Quality Assurance, and Regulatory Affairs functions, ensuring that operations, systems, and products consistently meet applicable GxP and global regulatory requirements. The Director of Quality and Regulatory Affairs will play a central role in defining an