Salario: Regulatory Affairs en España

Global ResponsibilityPlan, review, record, edit and answer questions from the work of analysts in the laboratory and, when appropriate, open OOS or deviations and notify Quality Assurance and plan, create tables, studies SAP introducing in climatic chambers and monitor samples of each batch; according to GMP regulations, operating procedures, Methods of Analysis, Good Laboratory Practices, Protocols and guidelines Stability direct superior; so that the results are consistent, to apply actions to correct deviations, duly recorded anomalous results, the study of stability, keeping the team updated and informed and, ultimately, confirm that batches behave like and registered. All this taking into account the safety regulations indicated by the company and the use of personal protective equipment provided depending on the risks of each operation.Specific ResponsibilitiesOrganize, supervise and control the work of the team responsible for the analysis and sampling of stability samples in the required timeframes.Review and approve stability documentation (analytical data).Creation and review of analytical methods and SOP and control that these procedures are properly implemented and followed by staff.Create stability protocol and reports.Ask for stability samples to start the required stability studies.Assure that all activities of the Laboratory follow approved method, SOP, quality guidelines, etc.Investigate the cause of deviations and OOS and propose corrective actions under QA Technicians coordination.Develop no routine activities carried out in the laboratory (including actions arising from deficiencies found in audits, CAPAs, deviations) so they can be finished within the required timeframe.Make order requests in SAP system for reagents, standards and all the materials and services necessary for activities developed in Quality Control Department.Provide technical assistance to analysts.Support Quality Assurance during customer and Authorities inspections of Quality Control Activities.Support Regulatory Affairs in the client or Authorities requests.Provide training of personnel following Quality Control training modules and annual training plan.Coordinate analytical methods implementation in Stability Area for new products stability studies.Review of stability chambers temperature and humidity taking actions if OOS of the parameters is detected.Train the new incorporations in the specific activities and functions of the position in which you are an expert.Competencies/Career levelInnovation, customer orientation, communication, teamwork, adaptability/flexibility, productivity, Self-development, sense of urgency, initiative.AccountabilitiesKPI related to the job.Requirements and personal skillsEducation: University degree in Chemistry or similar.Languages: High level of Spanish and English is necessary.Experience (years/area): Minimum 3-4 years’ experience in the functions mentioned above.Specific Knowledge: Knowledge of GMP and GLP regulationsTravels: Open to travelPersonal skills: good analytical skills, accuracy and reliable.COMMITMENT TO EQUAL OPPORTUNITIESLaboratorios Leon Farma / Farmalan is committed to equal opportunities.We do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

Johnson & Johnson MedTech is one of three successful divisions of the world's leading Johnson & Johnson family of companies.We are making an important contribution to the successful treatment of a wide range of common and chronic diseases with innovative - often pioneering - medical technologies and products.Are you ready to take your regulatory affairs career to the next level? Johnson & Johnson, a globally renowned family of companies committed to transforming healthcare, is currently recruiting for a Regulatory Affairs Leader - LATAM for our MedTech division.In this exciting role, you will have leadership responsibilities for Argentina, Brazil, Colombia, Peru, Ecuador, Panama, Costa Rica, and Mexico.Key Responsibilities.As the Regulatory Affairs Senior Director for Latin America, you will play a pivotal role in driving regulatory excellence across multiple countries.Your responsibilities include.·       Strategic Leadership.Lead our regional Regulatory Affairs teams in Argentina, Brazil, Colombia, Peru, Ecuador, Panama, Costa Rica, and Mexico.Develop and execute regulatory strategies to support and enhance business growth within the MedTech division.·       Visionary Strategy.Define a clear and influential future vision and strategy for regulatory affairs in the LATAM region.Align your strategies with global regulatory requirements and regional business objectives.·       Technological Advancement.Drive the adoption and utilization of cutting-edge technologies to optimize data-driven decision-making and enhance transparency in enterprise systems across Latin America.·       Strategic Planning.Establish short-term and long-term strategic goals, implementation plans, and provide guidance on regional, country, and cultural differences that may impact our business.·       Regulatory Engagement.Proactively shape the external regulatory environment and engage with regulators across Latin America to influence regulatory harmonization.·       Product Approvals.Accelerate product approvals by developing and executing regulatory strategies aligned with business objectives.Ensure product compliance with regulatory requirements and stay vigilant to regulatory changes.·       Budget Management.Take responsibility for detailed Regulatory Affairs budget planning and control.Manage projects and regulatory activities within timelines and budget requirements, while communicating the financial implications of regulatory activities on business results.·       Acquisitions and Divestitures.Support key acquisitions and divestitures by providing comprehensive regulatory assessments and the necessary expertise and resources.·       Collaborative Partnerships.Establish close and collaborative partnerships with business and functional stakeholders in the Latin American region, defining interdependencies and priorities.·       Cross-Functional Projects.Collaborate with Quality and Supply Chain teams on related projects to drive change management, labeling, cost improvement, and transformation projects, while providing timely regulatory assessments.·       Talent Development.Build a diverse and capable regulatory workforce, emphasizing the importance of recognizing and embracing cultural differences.Create a sustainable talent pipeline through recruitment, retention, and development strategies.·       Regulatory Excellence.Support the development of a regulatory sustainable model, focusing on process excellence, effective tools, systems, and efficiency improvements.·       Global and Regional Leadership.Act as an active member of the global regulatory affairs leadership team, advising on global strategy, regional impact, and priorities.Collaborate with business sector regulatory affairs and functional leaders to execute the global regulatory affairs strategy.This is a unique opportunity to lead regulatory affairs efforts across multiple countries in Latin America, making a significant impact on the healthcare industry in the region.If you are a dynamic and forward-thinking regulatory affairs professional with a passion for leadership and a desire to shape the future of healthcare through innovation and excellence, we invite you to join our team at Johnson & Johnson.Qualifications ·       A Bachelor's degree or higher is a must.We highly value advanced degrees and education in fields such as medicine, engineering, science, or law.·       You should bring a wealth of experience in a regulated industry, especially in management positions where you've successfully led teams.·       Medical device experience is preferred.Global franchise / business unit RA experience supporting an OUS market with diversity of experience – i..sector, company, function, product.·       Regulatory compliance risk evaluation and balanced decision making ·       Experience leading diverse teams in a matrix environment, cultural awareness, Talent Management in competitive markets ·       Large budget cost center management and business planning in a complex financial model ·       Regional or multi market experience with Regulatory Affairs, including Emerging market ·       Senior leadership experience is required, especially interacting with senior leaders and influencing strategy and decision making at senior levels ·       Demonstrated track record of formulating regional regulatory strategies that align with business deliverables is required.·       Experiences and leadership in working with external industry groups and International organizations is a plus; Outreach, influencing, negotiation, shaping, collaboration with Health authorities or industry trade groups ·       Strong English language (spoken and written) capability; other languages of regional countries are welcomed (Spanish/Portuguese) ·       Live the credo in a way that creates a trusting, collaboratively and ethical work environment ·       Strong Leadership Skills in Alignment with J&J Leadership Imperatives.Connect, Shape, Grow In this role, strong leadership is essential, aligning with the J&J Leadership Imperatives.·       Connect.Cultivate external relationships with regulators while fostering collaboration internally with the Franchise, Policy, and Central regulatory organizations, as well as other functions.·       Shape.Anticipate and influence regulatory changes to maximize patient access to innovative Franchise technologies.·       Lead.Acquire and develop a diverse team of talented regulatory professionals and communicate transparently and constructively.·       Deliver.Mobilize and inspire an accountable team to achieve results, ensuring on-time registrations with a global and enterprise-wide mindset while balancing strategic and short-term goals.If you possess these qualifications and are ready to make a significant impact in the field of regulatory affairs, we encourage you to explore this exciting opportunity with Johnson & Johnson.Join us in our mission to connect, shape, and grow in the pursuit of a healthier world for all.Johnson & Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.Employees may be eligible to participate in Company employee benefit programs such as health insurance, savings plan, pension plan, disability plan, long-term incentive, vacation pay, sick time, holiday pay, and work, personal and family time off in accordance with the terms of the applicable plans.Additional information can be found through the link below.  For additional general information on Company benefits, please go to.-  https://www.areers.nj.om/employee-benefits

our clientWe are currently seeking a Medical Affairs Publications Administrator for our client, a prominent Big Pharma company. The Global Medical Communications team is in search of an expert in Veeva Vault platforms who is dedicated to assisting team members in efficiently managing Medical Affairs publication deadlines.The person in this role will be responsible for submitting Medical Affairs scientific publications developed by the North America and International Medical Directors for medical and regulatory review and approval in top 12 countries and as required other nominated markets. These include new publications and existing publications that need to be repurposed/adapted for other countries. Additionally, the contractor will track international & local publication statuses (expiration dates, renewal of assets, distribution platforms) to ensure the meeting of submission deadlines. Lastly, contractor will be assisting with the dissemination process of these assets in our client Medical Affairs digital platforms for HCPs.your functions- Collaborates with North America and International Medical Directors to submit new and/or repurposed medical affairs assets for review and approval for all regions and ensures accurate submission details are captured for medical and regulatory approvals.- Collaborates with cross-functional colleagues in medical, regulatory, and legal to support the review and submission process in top 12 countries and as required other nominated markets.- Manages the company's medical asset library and tracking for assets from top 12 countries in partnership with the Medical Affairs Digital Platforms Manager and International Medical Communications Manager.- Manages medical affairs asset library and inputs metadata into platform to create website URLs in partnership with Global Medical Insights team.position requisitesFormación: GradoIdiomas: Inglés: C1Conocimientos: publicacionesExperiencia: 1 año- Bachelor¿s Degree or equivalent combination of experience of education and relevant experience- Previous experience in Medical Affairs or Ophthalmology/Optometry a plus - 1-4 years of relevant experiencewhy with Randstad?Because we have thousands of job offers in our portal.Because we work with the best companies offering you the best jobs.Because we assure you all the legal guarantees in your hiring.Because we guarantee a close follow-up after your incorporation, because we want you to be satisfied.Because we put at your disposal our advanced technology so that you can sign your contracts and access your labor documentation in a single click.Because we always count on you.Enroll in this offer, you will be part of the Randstad candidate database for future employment opportunities.Register now and find the job you are looking for!#weareSRCRandstad promotes equal employment opportunities through diverse and inclusive teams. Therefore, in our processes, we guarantee the inclusion of all people regardless of their personal condition, gender, sexual orientation, ethnicity, culture, age, religion or disability.#netZeroCommitmentRandstad encourages you to reduce your environmental impact to make your environment a better place for everyone. Our commitment to the Science Based Targets (SBTi) initiative, whose targets are based on science, drives Randstad ambition to be Net Zero by 2050.

At Johnson & Johnson, we believe health is everything.Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.nj.om/.  Janssen Research & Development, L.., a member of the Johnson & Johnson Family of Companies, is recruiting for a Director/Senior Director, Clinical Rseearch Physician for Late Development Oncology.  The preferred location for this position is Spring House, PA, but consideration could be given to other locations.Up to 25% travel may be required.Janssen Research and Development, L..., a member of Johnson & Johnson's Family of Companies, is recruiting for a Medical Director/Senior Medical Director-Clinical Research-Prostate.  They will be a member of a matrix team dedicated to the implementation of clinical research studies that are part of a global compound development program.  Responsibilities include.Directs Managers and/or senior individual contributors in a matrix environment, and is accountable for meaningful career development conversations and regular coaching and feedback.Leads execution of research programs for an area of clinical development to meet research objectives, support product development, and manage reports.Acts as the clinical functional head for providing active scientific contributions to a cross-department compound development team.Works in close partnership with the Compound Development Team (CDTL) and project management, global regulatory affairs, clinical pharmacology, health economics, and the disease area leader to share information.Acts as a liaison between the company and the clinical investigators, evaluates scientific information, and creates new ideas to assist in identifying new research opportunities.Develops the strategy and content for scientific communications for assigned compound through close partnership with the compound global medical affairs leader.Serves as the clinical leader for product evaluation and develops the strategy and the content for regulatory documents.Works with senior clinical staff, establishes credible relationships with external stakeholders such as opinion leaders and regulators, and provides substantial expertise in drug development (including experience with IND and NDA submissions).Able to manage study start-up, and directs and guides study team in study execution, data cleaning, medical review, database lock, managing health authority responses.May provide determination of pathology diagnosis and act as a signatory to primary and peer review pathology reports.Develops a goal-oriented clinical development team.Responsible for managing operational aspects of their teams (e.., budget, performance, and compliance), as well as implementing workforce and succession plans to meet business needs.Proactively creates a purpose driven environment by aligning Johnson & Johnson’s Credo and Leadership Imperatives with the strategies and goals of the team and enterprise.Qualifications An MD is required; Advanced degree (PhD) is a plus.  ·       A minimum of 2 years of oncology clinical research experience in clinical development within pharmaceutical industry or equivalent experience in academic or large regional hospital is required.  ·       Knowledge of Good Clinical Practices and regulatory requirements for the conduct of high quality oncology clinical trials is required.  ·       Experience in protocol development, medical review, oversight of study conduct, running trials, data quality and safety are strongly preferred.  ·       Working knowledge of the use of Microsoft suite of software products including Excel and Word is required.  ·       Fluent in written and spoken English with excellent communication skills is required.The anticipated base pay range for this position is $ to $.Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.ERADICATE CANCER

At Johnson & Johnson, we use technology and the power of teamwork to discover new ways to prevent and overcome the world’s the most significant healthcare challenges.Our Corporate, Consumer Health, Medical Devices, and Pharmaceutical teams leverage data, real-world insights, and creative minds to make life-changing healthcare products and medicines.We're disrupting outdated healthcare ecosystems and infusing them with transformative ideas to help people thrive throughout every stage of their lives.With a reach of more than a billion people every day, there’s no limit to the impact you can make here.Are you ready to re-imagine healthcare?   Here, your career breakthroughs will change the future of health, in all the best ways.And you’ll change, too.You’ll be inspired, and you’ll inspire people across the world to change how they care for themselves and those they love.Amplify your impact.Join us!   Johnson & Johnson is recruiting for a Summer Intern, located in Jacksonville, FL (hybrid).  Regulatory Affairs Opportunities.  Regulatory affairs is a profession developed from the desire of governments to protect public health by controlling the safety and efficacy of products in areas including pharmaceuticals, medical devices and consumer products among others, and by the companies responsible for the discovery, testing, manufacture and marketing of these products wanting to ensure that they supply products that are safe and make a worthwhile contribution to public health and welfare.  Key Responsibilities.  Experiences Include.  Assist in the compilation of requirements for global regulatory submissions of our products.  Support the acquisition and management of files to meet applicable regulations   Attend project team meetings with RA lead to assist in strategic discussions to hone team collaboration skillset   Learn regulatory affairs competencies to ensure product registration lifecycle processes compliance   Evaluate current processes and propose opportunities for efficiencies/improvements   Data analytics from regulatory information management systems (RIM) and reports / dashboards /presentations development.  US and Global Regulatory Policies Understanding and Shaping activities.  Qualifications Education.  Currently enrolled full-time and have completed at least 2 years in an undergraduate program, or enrolled full-time in a graduate program (M.., M.., Ph..or M..), pursuing a degree majoring in a scientific, technology, engineering, business or law related field.Examples include, biomedical, biochemical, civil, mechanical, or electrical engineering, data analytics/applied statistics, quantitative modeling in biology, pharmacy, pharmaceutical sciences, life sciences, medical / scientific writing or public health administration.  Candidate must be legally authorized to work in the United States and not require sponsorship for employment visa status (e.., H1-B status) now or in the future.  Experience and Skills.  Required.  Available to work full-time (40 hours per week) during Summer .  Candidates need to be proficient with Microsoft Office, Word, Excel (including a high proficiency with generating pivot tables and graphs), and Power Point, and have strong oral and written communication skills.  Additional technical competencies in SharePoint, Teams and other information technology systems are highly desirable.  Able to work individually, as well as, part of a group, with curiosity and flexibility.  Possess a “can do” approach, and courage to speak your voice and suggest innovative ideas.  Assignment location will be hybrid on-site in Jacksonville, Fl.  Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. 

Importante empresa multinacional del sector agroquímico ubicada en Murcia, está en búsqueda de un/a Regulatory Affairs junior.Esta posición desempeñará un papel crucial liderando y facilitando el proceso de registro de productos fitosanitarios, contribuyendo al cumplimiento normativo y la evaluación de riesgos ambientales asociados con productos de protección vegetal.Responsabilidades.Gestión de Dossiers Técnicos/as.Coordinar la preparación y presentación de dossiers técnicos/as, con especial énfasis en la sección de ecotoxicología, para respaldar la registración de productos de protección vegetal.Cumplimiento Normativo.Asegurarse de que todos los productos cumplen con las regulaciones y normativas en vigor en la Unión Europea, prestando especial atención a los aspectos de ecotoxicología.Interacción con Autoridades Regulatorias.Colaborar activamente con agencias reguladoras, responder a sus consultas y garantizar la aprobación oportuna de los registros.Evaluación de Riesgos Ambientales.Realizar evaluaciones detalladas de los riesgos ambientales asociados con los productos fitosanitarios, abordando posibles impactos en organismos no objetivo y en diversos ecosistemas.Colaboración Interdisciplinaria.Trabajar estrechamente con equipos multidisciplinarios, incluyendo científicos, toxicólogos/as y expertos/as en medio ambiente, para recopilar datos relevantes y garantizar la calidad de la información presentada.Actualización Normativa.Mantenerse informado sobre los cambios en las regulaciones y normativas, ajustando estrategias regulatorias en consecuencia.Requisitos Estamos en búsqueda de un/a profesional con formación en biología, agronomía u áreas relacionadas que esté interesado/a en adentrarse en el campo de Regulatory Affairs.Se requiere un nivel avanzado de inglés como requisito indispensable.Beneficios Posibilidad de combinar trabajo en oficina con teletrabajo.Modalidad freelance.Salario.€ /año

WeGrow is a dynamic, successful international specialty fertilizer marketer focused on quality and reliability. The company distributes a complete spectrum of water-soluble fertilizers and correctors and nitrogen inhibitors. Its logistics, production and distribution assets give it a competitive advantage. WeGrow’s identity is based on entrepreneurship, flat hierarchy and an exceptional team culture. WeGrow is seeking a highly motivated and detail-oriented individual to join the team as an International Regulatory Affairs Manager. In this role, you will be responsible for navigating the complex landscape of local and international trade regulations, preparing and maintaining the technical and safety documentation of the company´s product portfolio and obtaining import licenses, permits, in coordination with the Commercial Team and Legal Department to ensure compliance with regulatory and customs requirements in various countries. Key Responsibilities:Regulatory Research and Cross-functional Collaboration:Conduct thorough research on import regulations, licensing requirements, and customs procedures in target countries.Collaborate with cross-functional teams, including commercial and sales team, supply chain, legal, and finance, to ensure alignment with international trade regulations and commercial license requirements.License and Permit Acquisition:Initiate and manage the application process for import licenses and permits in accordance with local regulations.Collaborate with suppliers, customers, government agencies, customs authorities, and other relevant bodies to issue and provide the required dossiers and documents needed to obtain necessary license/permit approvals.Documentation and Record Keeping:Prepare and maintain accurate documentation for import licenses, permits, and customs compliance.Develop and maintain a comprehensive record-keeping system to ensure compliance with auditing standards. Prepare and maintain all labels, TDS and MSDS according to local and international regulations for the company´s product portfolio. Continuous Monitoring:Stay abreast of changes in international trade regulations and update internal stakeholders accordingly.Present regular reports to internal teams to keep the organization informed about changes in regulations and their potential impact. Qualifications:Bachelor’s degree in life sciences, environmental sciences, or related field Proven experience in quality control and/or quality assurance and/or international trade import/export regulations and obtaining licenses/permitsExcellent analytical, problem-solving, and communication skillsProficient in English and Spanish Personal Attributes: Detail-oriented with a strong commitment to accuracyAbility to work independently and collaboratively in a fast-paced environmentStrong organizational and time-management skillsAdaptability to evolving regulatory environmentsEthical and principled approach to international trade practices

¿Tienes experiencia previa como Regulatory Affairs Specialist?, ¿tienes experiencia en enfrentar y resolver desafíos regulatorios en un entorno dinámico?, ¿estás acostumbrado a asesorar sobre la clasificación adecuada de ingredientes y productos en función a las regulaciones vigentes? ¡Tenemos una propuesta para ti!Desde Eladiet, precisamos un Regulatory Affairs Specialist para nuestro Departamento de Regulatorio.¿Quiénes somos?Somos una empresa familiar ubicada en El Papiol (Barcelona) en la que, tras 35 años de apasionante trabajo, más de 140 personas colaboran a diario en el desarrollo de complementos alimenticios naturales, innovadores y eficaces.¿Cuáles serán tus funciones?Asegurar el cumplimiento de los requisitos legales vigentes aplicables a los productos y a la empresa.Custodiar y actualizar la documentación regulatoria (proveedores, autoridades sanitarias y entidades certificadoras, etc).Dar soporte regulatorio en la fabricación de productos para terceros desde el desarrollo hasta la fabricación y post comercialización.Solicitud de certificados de registros sanitarios, certificados APPCC, etc.Contribuir a la mejora continua de procesos y herramientas de trabajo aplicables al departamento.¿Qué esperamos de ti?Graduado/a en Farmacia con máster en la industria farmacéutica y parafarmacéutica o similar.Experiencia mínima de 3 años como técnico de registros en industria farmacéutica o similar.Nivel de inglés avanzado.¿Por qué Eladiet?Formarás parte de una empresa líder de un sector a fin al farmacéutico. A la vanguardia en la gestión de personas con talento.Trabajaras con un equipo joven y dinámico, en una empresa puntera en tecnología.Dispondrás de flexibilidad horaria desde el primer día.Disfrutarás de nuestras oficinas Open Space, rodeadas de naturaleza y diseño.Te ofreceremos formación On Boarding y continuada, además de clases de inglés totalmente gratuitas.¿Más beneficios? ¡Por supuesto!También de café gratuito todos los días.Disfrutarás de una sala con futbolín.¿Te atreves a aceptar nuestro reto?, ¡inscríbete, queremos conocerte!Conócenos mejor en:www.eladiet.comInstagram: @eladiet_#vivirnaturalmente

Proceso de selección continuo.FuncionesDo you have experience in supervising, preparing, and implementing protocols/reports for technology transfers? Are you looking for a new professional challenge?At Grupo Crit, we're looking for you!Global responsabilitiesMonitor, prepare and implement protocols/reports for technology transfers, manufacturing guides and provisioning orders, batches registration, industrial lots, working guidelines, documentation and reports and Standard Operational Procedures for Transfer; according to GMP regulations, SOPs, the Pharmacopeia of the various world regions and the guidelines of the manager; in order to ensure the correct execution and updating of the processes at an industrial level.The position involves coordinating and overseeing various aspects of product development and manufacturing within the pharmaceutical industry:1. Production Scaling: Supervise the transition of new development products from pilot to industrial scale, in collaboration with Formulation Development and Production teams.2. Product Scaling: Manage the pilot and industrial scaling-up of developed products.3. Formula and Process Improvement: Coordinate improvements in formulas or processes for existing products.4. Manufacturing Issue Resolution5. Customer Collaboration: Liaise with internal and external customers to address product transfer requirements.6. Regulatory Compliance: Manage documentation for pharmaceutical registration, ensuring compliance with governmental and legislative requirements.7. Batch Monitoring: Monitor batch production and registration processes, analyzing parameters and results, and preparing reports for Production and Quality Assurance departments.8. Technology Transfer9. Procedure Development10. Quality Assurance: Open and close change controls, deviations, or investigations as needed, ensuring compliance with quality standards.11. Interdepartmental Collaboration: Work with other departments to address project-related tasks promptly and effectively.RequisitosRequirementsEducation: Degree in Pharmacy. Master’s Degree in the pharmaceutical fieldLanguages: Fluent Spanish and English, knowledge of other languages will be an asset.Experience (years/area): +3 years of experience in a similar position, in formulation, production o tech transfer in the pharma industry.Specific Knowledge: GMP, GLP, ICH and FDA regulations and Tech Transfer procedures. Knowledge of formulation development (equipment and production processes), Regulatory affairs knowledge. Solid products knowledge.