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📢 Are you looking for an opportunity to develop your professional career in a CDMO Quality Control Department? The successful candidate will join 3PBiovian as a Senior Physicochemical Laboratory Technician- Quality Control. 🚀Main responsibilities: • Planning of the laboratory activities. Ensure their compliance and to manage human resources according to the planning and needs of the processes., • Guarantee the accuracy of the results issued by the Laboratory., • Manage, supervise and generate technical documentation associated such as: SOPs and CoAs., • Coordinate the correct state of work equipment according to GMP requirements and technical data sheets., • Manage and investigate OOS and deviations as needed., • Ensure the application of GMP requirements and the correct training of the personnel in charge. 📖 Assesment criteria: • University degree or equivalent in Chemistry, Biochemistry; Biology; Biotechnology or related areas., • Master's degree in Chemistry; Biochemistry; Biology; Biotechnology or related areas., • PhD in related areas is desirable, but not necessary At least 7 years of experience with/ in: • Experience on GMP regulations., • Extensive technical knowledge on analytical biochemical, bioassay and microbiological methods., • Experience in international environments is a plus., • Managing a technical team in a Laboratory. 💊Why 3PBiovian? • You will have 26 paid days off: 23 vacation days + 2 personal days + 1 day off set by the company., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income tax (childcare, health insurance, training, etc.)., • Company benefits club, which allows 3P employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, Fnac, Rituals, El Corte Inglés, etc.)., • Flexible working hours during the week and a reduce work day on Friday of 7h., • Special Summer working day of 7 hours during July and August, as well as 7-hour working days during the first week of September and the last week of December, • 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees., • The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces., • We have a high-impact work environment with flat hierarchies and short decision-making processes., • All new hires who reside outside of Navarra are provided with a relocation service and/or assistance. 💥Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and cGMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human an animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. 🌟It's within us.

📢 Are you looking for an opportunity to develop your professional career in a CDMO Quality Control Department? The successful candidate will join 3PBiovian as a QC Supervisor Technician Physicochemical Laboratory. 🚀Responsibilities: • Ensure GMP activities in the physicochemical laboratory., • Evaluate and review the technical documentation corresponding to the Quality Control of the physicochemical laboratory, as well as the analytical results in routine manufacturing, validation and transfer activities., • Organize and ensure compliance with the weekly program and coordinate human, material and technical resources to ensure its achievement., • Propose process improvements aimed at improving quality, cost, performance, time and safety of workers and the environment., • To train and qualify the analysts to carry out the controls correctly., • Maintain the installations in perfect state of conservation ensuring that they are operated according to the manuals provided by the manufacturer., • Carry out the drafting and supervision of standard operating procedures (SOP's)., • Carry out the resolution of deviations in the laboratory., • Coordinate the release of raw materials and the analysis of intermediates, drug substances and drug products., • Support stability studies agreed with our customers in collaboration with other technicians., • Provide production quality support in case of incidents that may arise., • Approve and close CAPAS (corrective and preventive actions) arising from deviations and applicable efficacy verification., • Check the correct traceability of the materials consumed in the analysis process., • Perform duties as assigned and for which job training has been received. 📖 Assesment criteria: • University Degree or equivalent in Chemistry; Biotechnology; Biology or similar., • Master's degree related to the area of study., • PhD in a related area is valued, but not necessary, • Intermediate level of English (B1 level / First Certificate), • Open to work in shifts. At least 4 years of work experience in/with: • Use of techniques such as HPLC, UV and IR Spectrophotometry, UPLC, Fluorescence, DAD, UV-VIS…, • Experience with recombinant proteins, mAbs, Biosimilar, ADCs (desirable)., • Experience with pharmaceutical regulatory guidelines., • Use of Agilent equipment with Empower 3 software. ❗️❗️Why 3PBiovian? • A permanent and stable position in a competitive growing company., • A competitive time off package with 39 paid days of vacation., • Additionally you will have an extra day off on the 26th of December., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.), • Company benefits club, which allows 3P Biovian employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • ...And so much more! 💥Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and cGMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human an animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. 🌟It's within us.

📢 Are you looking for an opportunity to develop your professional career in a CDMO Analytical Methods Development Department? The successful candidate will join 3PBiovian as an AMD Physicochemical Laboratory Technician. 🚀Responsibilities: • Coordinate developments, implementations, qualifications and transfers of physicochemical analytical methods and n this activity includes the design of experiments, review of documentation and associated data and the generation of protocols, reports and / or presentations required., • Supervise the execution of sample analyses carried out in the laboratory, as well as the review and communication of the results obtained., • Develop standard operating procedures related to analytical methods, as well as other procedures related to the operation of the area., • Prepare protocols, reports, as well as final reports of stability studies, forced degradation studies, characterization of reference materials, re-testing of reference materials, investigations and other non-GMP studies that are not included in the above descriptions., • Manage stability studies, sample and sample location control, analysis times and execution of analytical runs., • Participate in technical meetings., • Maintain fluid communication with the departments involved., • Participate in the proposal of operational improvements oriented to the quality and efficiency of the work., • To write the transfer protocols of the Physical-Chemical methods., • Technical responsibility for the activities developed within the framework of the projects assigned to them. 📖 Assesment criteria: • University degree or equivalent in related areas: Biochemistry; Biology; Biotechnology; Chemistry, etc., • Valuable but not necessary Master's Degree related to the area (Chemistry; Biochemistry; Biotechnology; Biology, etc.)., • Valuable but not necessary Phd with specialization in Biotechnology., • Advanced level of English Level, C1 / Advanced. Language certificate not required; placement test will be administered., • Open to work in shifts. Between 3 and 4 years of experience in: • Pharmaceutical, biopharmaceutical, biotechnological sector or research centers., • Analytical techniques such as: HPLC; UPLC; Fluorescence; DAD; UV - VIS, UV Detection; PDA/dad; ELSD/CAD/MS., • Experience with recombinant proteins, mAbs, Biosimilar, ADCs., • Participation in analytical method development design., • Method validations (valuable)., • Handling of Agilent equipment with Empower 3., • Supervision and coordination of personnel., • Participation in technical meetings with customers., • Valuable knowledge in GMP regulations and in the qualification/validation of analytical methods. 💊Why 3PBiovian? • A permanent and stable position in a competitive growing company., • A competitive time off package with 39 paid days of vacation., • Additionally you will have an extra day off on the 26th of December., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.), • Company benefits club, which allows 3P Biovian employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • ...And so much more! 💥Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and cGMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human an animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. 🌟It's within us.

📢We are looking for a results-driven, innovative, and motivated Head of Business Development to join our Business Development team. 🚀Main Responsibilities: As a Head of Business Development, your responsibilities will include: • Identify and contact potential clients, as well as detect and define their needs., • Conduct continuous market analysis, including potential clients, key players, and competitors., • Prepare commercial offers., • Negotiate the presented proposals until the signing of the LOI or Contract, playing a leading role in advanced negotiations., • Coordinate with the technical team to develop proposals, including technical scope and project timeline definition., • Plan, guide, control, and supervise the business development activities of the assigned team., • Monitor team performance and achievement of results., • Collaborate with the Marketing Department on advertising strategies targeting the market and clients., • Attend client visits to 3PBIOVIAN facilities, trade fairs, or client locations, as well as provide support in the preparation of trade fairs and conferences. 📚Assessment Criteria: • Education: Bachelor's degree in Biological Sciences, Biochemistry, Biotechnology, Pharmacy, Chemical Engineering, or Chemistry. A Master's in Business Administration or a related field is desirable. A PhD in Biological Sciences, Biochemistry, Biotechnology, Pharmacy, or Chemistry would be a plus., • Languages: Fluent in Spanish and English. Knowledge of additional languages is an advantage., • Experience: 6+ years of experience in a similar position in CDMO companies within the Biopharmaceutical sector. 💊Why 3PBiovian? • You will have 26 paid days off: 23 vacation days + 2 personal days + 1 day off set by the company., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income tax (childcare, health insurance, training, etc.)., • Company benefits club, which allows 3P employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, Fnac, Rituals, El Corte Inglés, etc.)., • Flexible working hours during the week and a reduce work day on Friday of 7h., • Special Summer working day of 7 hours during July and August, as well as 7-hour working days during the first week of September and the last week of December, • 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees., • The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces., • We have a high-impact work environment with flat hierarchies and short decision-making processes., • All new hires who reside outside of Navarra are provided with a relocation service and/or assistance. 💥Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and cGMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human an animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. 🌟It's within us.

🚀 About us Viscofan is the world leader in the production and distribution of casings for the meat industry. With operations in more than 110 countries and a team of over 5,500 people, we combine industrial excellence and innovation to lead both the food and biotechnology markets. Join our global team as a Product Marketing Manager in our Nutra Medical Business Unit, where you'll play a pivotal role in shaping the future of health solutions across nutraceuticals, pharmaceuticals, and biomaterials. Your mission will be to lead the full lifecycle of health-related products—from development to market launch—ensuring strategic positioning, regulatory compliance, and commercial success. You will act as a key connector between R&D, production, regulatory, and commercial teams, driving innovation and growth in a highly regulated and competitive industry. Key responsibilities: • Manage product portfolio and lifecycle, adapting to market and regulatory changes, • Define product strategy: positioning, segmentation, value proposition, competitive differentiation, • Conduct market research and competitive intelligence in nutraceuticals and biomaterials, • Collaborate with cross-functional teams (R&D, QA, Regulatory, Production, Marketing) for product development, • Create scientific marketing materials: technical sheets, clinical evidence, white papers, • Execute marketing mix strategies (online/offline), including digital campaigns, events, and PR, • Support sales teams with training, tools, and demand generation initiatives, • Represent the company at trade shows, congresses, and product launches, • Build relationships with KOLs and technical stakeholders, • Manage marketing budgets and justify investments Qualifications and key competencies: • Bachelor’s degree in Health Sciences, Pharmacy, Biotechnology, Biology, chemistry (combined with Marketing studies background) or Marketing Bachelor´s degree (combined with technical/scientific background), • Minimum 10 years’ experience in product marketing within health-related industries (nutraceuticals, supplements, medical devices, pharma), • Strong knowledge of health regulations, claims, GMP, and certifications (FDA, EFSA, ANMAT), • Fluency in English and Spanish. German is a plus. Technical expertise in: • Market analysis tools (quantitative & qualitative), • CRM, marketing automation, SEO/SEM, BI tools, e-learning platforms, • Product innovation methodologies (Agile, Stage Gate), • Functional ingredients, APIs, biomaterials (collagen, biopolymers, delivery systems), • Formulation of supplements, drugs, and medical devices, • Business models: B2B, B2C, pharmacy channel, e-commerce, export 🌍 Why Join Viscofan? • Contribute to impactful projects with a global footprint., • Be part of a committed, international team working on innovation and continuous improvement., • Develop your career in a stable, growing company that invests in people and technology., • Enjoy a collaborative, down-to-earth work environment with clear purpose and long-term vision. At Viscofan, we believe in building a diverse, inclusive, and empowered team. We welcome professionals who bring vision, execution, and leadership to the table.

Are you looking for an opportunity to develop your professional career in a CDMO Analytical Methods Development Department? The successful candidate will join 3 PBiovian as an AMD Physicochemical Laboratory Technician. Responsibilities: Coordinate developments, implementations, qualifications and transfers of physicochemical analytical methods and n this activity includes the design of experiments, review of documentation and associated data and the generation of protocols, reports and / or presentations required. Supervise the execution of sample analyses carried out in the laboratory, as well as the review and communication of the results obtained. Develop standard operating procedures related to analytical methods, as well as other procedures related to the operation of the area. Prepare protocols, reports, as well as final reports of stability studies, forced degradation studies, characterization of reference materials, re-testing of reference materials, investigations and other non-GMP studies that are not included in the above descriptions. Manage stability studies, sample and sample location control, analysis times and execution of analytical runs. Participate in technical meetings. Maintain fluid communication with the departments involved. Participate in the proposal of operational improvements oriented to the quality and efficiency of the work. To write the transfer protocols of the Physical-Chemical methods. Technical responsibility for the activities developed within the framework of the projects assigned to them. Assesment criteria: University degree or equivalent in related areas: Biochemistry; Biology; Biotechnology; Chemistry, etc. Valuable but not necessary Master's Degree related to the area (Chemistry; Biochemistry; Biotechnology; Biology, etc.). Valuable but not necessary Phd with specialization in Biotechnology. Advanced level of English Level, C1 / Advanced. Language certificate not required; placement test will be administered. Open to work in shifts. Between 3 and 4 years of experience in: Pharmaceutical, biopharmaceutical, biotechnological sector or research centers. Analytical techniques such as: HPLC; UPLC; Fluorescence; DAD; UV - VIS, UV Detection; PDA/dad; ELSD/CAD/MS. Experience with recombinant proteins, m Abs, Biosimilar, ADCs. Participation in analytical method development design. Method validations (valuable). Handling of Agilent equipment with Empower 3. Supervision and coordination of personnel. Participation in technical meetings with customers. Valuable knowledge in GMP regulations and in the qualification/validation of analytical methods. Why 3 PBiovian? A permanent and stable position in a competitive growing company. A competitive time off package with 39 paid days of vacation. Additionally you will have an extra day off on the 26th of December. Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.) Company benefits club, which allows 3 P Biovian employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.) All new hires who reside outside Navarra are provided with a relocation service and/or assistance. ... And so much more! Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and c GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human an animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. It's within us.

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Coordinador y líder de proyectos e-commerce, gestionando equipos multidisciplinarios y asegurando la comunicación a nivel ejecutivo.

The Role: Data Delivery Manager.

Buscamos repartidores nocturnos para entregar pedidos a domicilio, ofreciendo un salario fijo mensual y oportunidades de crecimiento profesional.

The Role: Data Delivery Managerreports to Head of Toolchain ManagementAs a Data Delivery Manager, you’ll take ownership of all data records within the Digital Profile Factory (DPF) and define master data sources, ensuring accuracy and consistency across systems. At G+D Mobile Security, a world lea