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We are looking for a Regulatory Affairs / Clinical Affairs Specialist with strong experience in pharmaceuticals and medical devices. Descubra exactamente qué habilidades, experiencia y cualificaciones necesitará para tener éxito en este puesto antes de enviar su solicitud a continuación. Your Responsibilities: • Manage regulatory projects in pharmaceuticals and medical devices, • Advise clients on regulatory compliance, product registration, and market access, • Prepare and submit regulatory dossiers to competent authorities, • Monitor regulatory changes and anticipate legislative developments, • Support clients during audits and inspections, • Optimize internal processes related to compliance and quality, • Deliver training and guidance to client teams on regulatory requirements, • Collaborate with multidisciplinary teams to ensure project success Your Qualifications: • Experience in regulatory affairs for pharmaceuticals and medical devices (5-15 years), • Proficiency with industry-specific tools and software, • Academic background in Life Sciences, Pharmacy, Engineering, or related field, • English fluent. French is a plus., • You demonstrate strong analytical and problem-solving skills, • You demonstrate excellent communication skills What You’ll Get From Us: • Be part of a very international and diverse team, • Part-time work from home and work from office, • Ability to work from different offices in different cities and countries, • Long-term career planning as part of periodic performance reviews, • Professional development plans are tailored to each member of the team, • Ability to branch out into other areas such as market access, pricing, statistics, RWE, etc., • Strong opportunity to bring in your ideas and leave your mark on the organization, • Competitive salary and compensation Amaris Consulting is committed to diversity and inclusion. xcskxlj We welcome applications from all qualified individuals, regardless of gender, sexual orientation, race, ethnic origin, beliefs, age, marital status, disability, or any other characteristic.

Amaris is looking for a Data Manager with strong experience in clinical data management for CRO environments. The position focuses on supervising data management activities to ensure the smooth progress and quality of clinical projects. ¿Es este el siguiente paso en su carrera? Descubra si es el candidato adecuado leyendo la descripción completa a continuación. Your Responsibilities • Act as the main point of contact for all data management topics and participate in project/study meetings, • Contribute to the selection of subcontractors by preparing specifications and evaluating proposals, • Participate in study design, including data management sections in protocols and CRF specifications, • Oversee outsourced data management activities, ensuring compliance with cost, timelines, and data quality, • Validate deliverables such as data management plans, validation plans, transfer specifications, eCRF completion guides, and coding instructions, • Test eCRF before production deployment and after each protocol amendment, • Implement targeted quality control of data based on risk assessment, • Monitor progress of data management steps (entry, cleaning, coding, external data transfers, SAE reconciliation, etc.), • Approve SDTM specifications and verify SDTM packages as needed, • Regularly assess subcontractor service quality, establish action plans for deviations, and discuss corrective measures, • Participate in data review meetings and validate associated reports, • Ensure responsibility for database lock and unlock, verifying all prerequisites, • Provide statisticians with data for statistical analysis, • Verify the presence of all data management documentation in the Trial Master File (TMF) Your Qualifications • Experience in clinical data management for CROs (5–10 years), • Proficiency with industry-standard data management tools and software, • Academic background in Life Sciences, Pharmacy, or related field, • English fluent. French is a plus., • You demonstrate strong analytical and problem-solving skills, • You demonstrate excellent communication skills What You’ll Get From Us • An international community bringing together 110+ different nationalities, • An environment where trust has a central place: 70% of our key leaders started their careers at the first level of responsibilities, • A robust training system with our internal Academy and 250+ available modules, • A vibrant workplace that frequently gathers for internal events (afterworks, team buildings, etc.), • At Mantu, sustainability is part of everything we do. You’ll have the opportunity to turn your ideas into action and make a tangible impact. Every day, our teams bring our ESG commitments to life, from reducing our footprint to driving positive change within our communities. Through our WeCare Together program, you’ll be empowered to design and lead projects that create real social or environmental impact, with the company’s full support. Amaris Consulting is proud to be an equal-opportunity workplace. We are committed to promoting diversity within the workforce and creating an inclusive working environment. xcskxlj For this purpose, we welcome applications from all qualified candidates regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.

We’re Hiring: Key Account Manager (Europe) – NeilMed Pharmaceuticals ¿Tiene las siguientes habilidades, experiencia e impulso para tener éxito en este puesto? Descúbralo a continuación. NeilMed Pharmaceuticals is looking for a Key Account Manager (KAM) to join our European team. This role will focus primarily on the Spanish market, managing strategic relationships with pharmacy cooperatives and pharmacy groups, while also providing commercial support across several European markets, including Germany, Italy, France, and Portugal. Key Responsibilities • Develop and manage relationships with pharmacy cooperatives and pharmacy groups in Spain, • Identify growth opportunities and implement commercial strategies to increase distribution and sales, • Support commercial activities in wholesaler in Germany, Italy, France, and Portugal, • Work closely with local distributors and partners to strengthen NeilMed’s presence in each market, • Monitor market trends, competitor activity, and customer needs, • Collaborate with the global team on sales strategy, forecasting, and product positioning Profile • Proven experience as Key Account Manager / Sales Manager in healthcare, pharmacy, OTC, or medical devices, • Strong understanding of the pharmacy channel and distribution networks in Spain, • Experience working with international markets is a plus, • Excellent relationship-building and negotiation skills, • Fluent Spanish and English (additional European languages such as German, French, Italian, or Portuguese are a xcskxlj strong plus), • Ability to work in an international and fast-growing environment What We Offer • Opportunity to join a global leader in nasal care and medical devices, • A strategic role with international exposure, • Competitive compensation package, • Dynamic and collaborative team environment, • If you are interested or know someone who could be a great fit, please feel free to reach out or apply via LinkedIn message.

We are partnering with an international healthcare organisation seeking a Cualquier información adicional que necesite para este trabajo se encuentra en el texto a continuación. Asegúrese de leerla detenidamente y luego envíe su solicitud. Strategic Planning & PMO Director to drive strategic execution across the business. This is a senior leadership role designed to strengthen the company’s strategic planning capabilities and execution model, ensuring that corporate priorities are translated into clear initiatives and delivered with impact across the organisation. About the Role Reporting to the Corporate Services Director , the Strategic Planning & PMO Director will lead both Strategic Planning and PMO, acting as a key partner in shaping, structuring and executing the company’s strategic roadmap. The role combines long-term strategic thinking with strong industrial execution, moving beyond traditional project management to drive organisational alignment, prioritisation and delivery discipline. Key responsibilities include: Leading corporate strategic planning processes and supporting the definition of strategic priorities Translating strategy into a structured and prioritised portfolio of initiatives Governing execution of strategic programmes including NPD, lifecycle management and cross-functional transformation initiatives Ensuring alignment between strategic ambition, operational capabilities and resource allocation Providing executive-level insight and reporting to senior leadership Strengthening project governance, methodologies and execution standards across the organisation Acting as a senior change leader and trusted partner to business leaders Leading and developing the PMO team and overseeing corporate SAP Master Data governance Ensuring initiatives deliver measurable business and organisational value within a regulated healthcare environment Profile We are looking for a senior leader combining strong industry experience with proven ownership of strategic planning and execution . The ideal candidate will bring: Solid industry experience in strategic planning, business transformation, PMO leadership or strategy execution roles Demonstrated experience participating in or leading corporate strategic planning processes Experience operating within complex industrial or healthcare environments Strong ability to bridge strategy definition and operational execution Previous consulting experience is highly valued as complementary exposure, particularly when followed by industry leadership roles Excellent stakeholder management and executive communication skills University degree in Engineering, Life Sciences, Pharmacy, Business Administration or related fields Project Management training or certification is a plus Fluency in English and Spanish Why consider this opportunity This position offers the opportunity to operate at the centre of strategic decision-making within a growing healthcare organisation, influencing both where the company is going and how it gets there. xcskxlj For a confidential discussion, please apply today.

Our client, a spin-off from the University of La Coruña (UdC) has developed a novel handheld bioprinting device (“biopen”) and a complementary photosensitive bioink for in situ regeneration of oral soft and hard tissues. They are looking for a CEO with successful commercial and fund-raising experience. Beyond these most important managerial areas, the CEO needs to have knowledge and capacity to accomplish regulatory and administration issues. Asegúrese de leer la descripción completa a continuación y, si confía en que cumple todos los requisitos, envíe su solicitud de inmediato. Key Duties and Responsibilities: • Design and implementation of a sound business plan for Newco, including financial projections and funding needs., • Commercial & Business development responsibilities and organic growth., • Securing private funding (Seed & Series A round) and other non-dilutive financing options., • Strategic planning to maximize the creation of value and risk-manage challenges and opportunities., • Communicating, on behalf of the company, with stakeholders such as partners, investors, and potential clients., • Maintaining awareness of the competitive market landscape, expansion opportunities, industry developments, etc. Qualifications, Knowledge, and Experience: • Solid experience in commercial & managerial positions (C-level would be valued), part of it acquired in international companies., • A university degree in science (chemistry, biology, pharmacy) or business administration.; PhD degree and/or MBA would be valued., • Experience in oral markets and with oral products would be highly valued., • Working experience in the life science companies and interactions with venture capital investors in relation to financing rounds (Seed and Series A)., • Administration and Management — Knowledge of business and management principles involved in strategic planning, resource allocation, human resources modelling, leadership technique, production methods, and coordination of people and resources. Skills and Abilities - The successful candidate will/must: • Have strong commercial, problem-solving and analytical skills as well as self-confidence and versatility., • Have excellent leadership and interpersonal skills., • Be willing and able to be “hands on”., • Read, write, and speak English fluently. xcskxlj We are looking for a Part-Time CEO; the position can be remote with trips to La Coruña when necessary.

About Us: Todas las habilidades, cualificaciones y experiencia relevantes que necesitará un candidato seleccionado se enumeran en la siguiente descripción. 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: This role will deliver the assigned R&D projects with defined quality, time and cost. In addition, you will provide the necessary technical support for the products currently on the market. Responsibilities: • Lead or participate in project teams focused on developing new products or improving existing ones., • Design development plans for research projects, defining objectives, methodologies, and timelines., • Plan, supervise, and execute internal experimental work, ensuring the correct application of protocols, the proper use of resources, and the quality of the results obtained., • Plan, execute and monitor studies in collaboration with external centres, ensuring technical and operational consistency., • Apply statistical and bioinformatic tools for the analysis of experimental data, interpretation of results and evidence-based decision-making., • Ensure the delivery of projects on time, on budget and with the required quality., • Scientifically evaluate new ideas and research proposals., • Manage technical knowledge with internal and external experts., • Communicate R&D project results to the business units involved., • Provide scientific and technical training, both internally and externally., • Review technical documentation and resolve scientific queries from the team or other areas., • Participate in relevant scientific conferences, seminars and events. About You: • Minimum 2 years' experience in R&D., • Degree in Chemistry, Biotechnology or Pharmacy, or demonstrable equivalent experience., • Fluent English., • Postgraduate degree in project management 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 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: 2nd April 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. xcskxlj Our goal is to ensure equal opportunities and actively combat discrimination – both in the application process and in everyday working life.

About ¿Interesado en saber más sobre este trabajo? Desplácese hacia abajo y descubra qué habilidades, experiencia y cualificaciones académicas se necesitan. ANA B ION We are ANA B ION , an international biotech company dedicated to helping people live longer and healthier lives. Our strong portfolio spans effective, safe, and affordable solutions in Life Sciences, including innovative treatments, biosimilars, and gene therapies for oncology, autoimmune disorders, and rare diseases such as SMA and hemophilia. About the Role We are seeking a Global Regulatory Affairs Manager who will play a pivotal role in advancing our international portfolio (spanning high‑technology biological products) across markets in Asia, Africa, the Middle East, Latin America, and Europe. In this role, you will lead and coordinate global regulatory activities, from strategy development to the preparation and submission of dossiers for multiple regions. You will work closely with regulatory authorities, partners, and cross‑functional teams, ensuring timely approvals, efficient life‑cycle management, and full compliance with diverse international requirements. This position is ideal for an experienced regulatory leader who thrives in a dynamic, multicultural environment and is ready to take ownership of complex global processes while guiding and empowering a distributed regulatory team. Responsibilities: Manage a team of at least 10 RAMs across various international regions (Asia, Africa, the Middle East, Latin America) to ensure the execution of international product registration processes for ANA B ION's portfolio in foreign markets. Oversee the preparation and submission of registration dossiers in foreign countries across Asia, Africa, the Middle East, Latin America, and Europe. This includes initial registrations, dossier updates, registration renewals, pharmaceutical expertise submissions, and responses to additional inquiries from regulatory authorities and partners. Work includes handling registration dossiers for high‑technology biological medicinal products. Develop regulatory strategies for the department’s registration projects in accordance with legislative and internal timelines, and maintain valid marketing authorizations for medicinal products in Asia, Africa, the Middle East, Latin America, and Europe. Interact with regulatory authorities in Asia, Africa, the Middle East, Latin America, and Europe, as well as with partners and contractors within the framework of contractual registration activities. Develop the department’s budget and monitor its execution. Oversee the accuracy and completeness of information related to all departmental registration processes within the company’s internal systems. Draft and coordinate regulatory legal acts within the company’s legislative initiatives and participate in regulatory working groups. Professional Knowledge and Skills: Higher education in Law or Pharmacy. 5+ years of experience in a senior regulatory leadership role with full responsibility for international registration processes. Proven expertise in building, managing, and optimizing regulatory workflows across multiple international markets. Strong understanding of international regulatory frameworks and requirements for the registration and development of biological products. Hands‑on experience with preparation, submission, and maintenance of registration dossiers, including initial registrations, variations, renewals, and responses to authority inquiries. Experience working with biological / high‑technology medicinal products and corresponding regulatory dossiers. Ability to oversee regulatory strategy development, ensuring compliance with legislative timelines and diverse regional regulations. Fluency in English at Advanced level (C1). Competencies and Soft Skills: Strong leadership and people‑management skills, including experience overseeing teams of regulatory professionals across multiple countries. Excellent cross‑cultural communication and the ability to collaborate effectively with stakeholders in varied geographic and regulatory environments. High degree of organizational and project‑management skills, capable of coordinating multiple parallel submissions and timelines. Strategic mindset with the ability to make informed decisions, anticipate regulatory risks, and proactively adjust strategies. Strong attention to detail combined with the ability to navigate complex regulatory documentation and requirements. Ability to manage external interactions confidently, including regulatory authorities, partners, and contractors. Problem‑solving orientation and resilience in navigating evolving regulatory environments. Commitment to ensuring compliance, quality, and operational excellence in all regulatory processes. What We Offer: Access to global expertise, international cross‑functional collaboration, and long‑term career development within ANA B ION . A results‑driven environment where strong performance is recognized and rewarded. The opportunity to play a meaningful role in building an ambitious, fast‑growing global biotechnology company. xcskxlj A competitive compensation package with performance‑based bonuses.

Do you want to be part of a team with a real impact on global health? ¿Es este su próximo empleo? Descúbralo leyendo la descripción completa a continuación y no dude en enviar su candidatura. At Noucor , a chemical and pharmaceutical company, we offer you the opportunity to lead projects that reach more than 100 countries worldwide . We are currently looking for a Clinical R&D Quality Assurance Technician to join Noucor’s Quality team. Main Tasks: • Ensure that all processes related to clinical trials are performed in compliance with GCP (Good Clinical Practice) and applicable quality standards., • Provide QA support to clinical trial activities, including documentation review and quality oversight of internal teams and external partners (CROs, service providers)., • Evaluate and manage quality issues, deviations, CAPAs, change controls and complaints related to Clinical Trials., • Support quality activities related to Investigational Medicinal Products (IMPs) in collaboration with Pharmaceutical Development and Analytical Development., • Degree in Pharmacy, Chemistry, Biology, or similar., • Fluent in English and Spanish., • Experience in Good Clinical Practices (GCP); knowledge of GMP requirements for IMPs in clinical trials (formerly Annex 13)., • Good command of MS Office., • High willingness to learn and take on new challenges and responsibilities. xsgfvud