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Si te apasiona la industria farmacéutica y cuentas con experiencia como analista QC, ¡esta es tu oportunidad! En Inmunotek estamos creciendo y por ello necesitamos incorporar a nuestro departamento de Control de Calidad un/a Analista QC Fisicoquímico en nuestra planta de Alcalá de Henares. Te encargarás de: • Ejecución de técnicas. tales como Karl Fisher, Bradford, ELISA competición, valoraciones potenciométricas, determinación Nitrógeno total, Determinación Carbono orgánico Total, conductividad, SDS-Page, Western Blot., • Comprobar la cualificación y calibración necesaria de los distintos equipos de Control de Calidad, así como asegurar su correcto manejo y mantenimiento., • Cumplimentar la documentación relacionada con el área de Control de Calidad Físico-Químico., • Participar en la redacción de Procedimientos Normalizados de Trabajo (PNTs) en Control de Calidad., • Participar en la mejora continua de los procesos, identificando mejoras en el puesto de trabajo y en los procedimientos. ¿Qué buscamos? • Conocimientos en técnicas básicas de control fisicoquímico., • Destreza en el laboratorio en materia de manejo de pipetas, preparación de reactivos, etc., • Habilidades en el cumplimiento de procedimientos y normativa de Calidad., • Acostumbrado/a a trabajar con Excel, Access., • Conocimientos en LIMS., • Buena capacidad de análisis e interpretación de los resultados obtenidos. ¿Qué ofrecemos? • Contratación temporal., • Condiciones económicas según valía del candidato/a., • Jornada completa de L-V horario de mañana., • Tendrás la oportunidad de trabajar en una empresa consolidada dentro de la industria farmacéutica que te permitirá continuar con tu desarrollo profesional. En Inmunotek trabajamos por crear un entorno laboral más diverso e inclusivo, apostando por el Talento de las Personas, sin centrarnos en etiquetas. Estamos comprometidos con la no discriminación por razón de raza, edad, sexo, estado civil, ideología, nacionalidad, religión, orientación sexual, discapacidad o cualquier otra condición personal. Si lo que has leído hasta ahora encaja contigo, ¡envíanos tu CV que estaremos encantados de conocerte!

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob Description At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner, and safer. We provide our teams with the resources needed to achieve individual career goals while advancing science through research, development, and delivery of life-changing therapies.With clinical trials conducted in over 100 countries and ongoing development of innovative frameworks for clinical research through our PPD portfolio, our work spans laboratory, digital, and decentralized clinical trial services. Your dedication to quality and accuracy will improve health outcomes for communities worldwide.We are seeking an Executive Director, Business Development, to join our Real World Evidence business development team within the Clinical Research Group of Thermo Fisher Scientific.Summary The Executive Director, Business Development, leads a team of business development representatives to secure and retain business for PPD through professional, consultative sales activities targeting sponsors' decision-makers and influencers. The role focuses on positioning PPD as a preferred provider for outsourced work in Health Economics, Market Access, Patient-Centered Research, and Data Analytics.This role involves mentoring staff, developing strategies, and overseeing business development initiatives with authorization goals ranging from $100 million to $500 million based on the region.Responsibilities Lead business development initiatives and develop marketing strategies for growth.Mentor staff in generating new business and expanding existing accounts, including negotiating and closing contracts.Manage client relationships, ensure satisfaction, and address any issues.Establish strategic direction aligned with senior management goals.Develop interpersonal relationships to influence decision-makers within and outside the company.Qualifications Minimum 15+ years of relevant experience, including 10+ years of management responsibility.Proven sales success in RWE, with international experience and account management skills.Strong network of mid- and high-level business contacts.Ability to manage cross-functional teams and develop sales leads.Expertise in Health Economics, Outcomes Research, Market Access, Data Analytics, and Patient-Centered Research.Working Conditions Office environment with travel up to 60% depending on activity and client needs.What We Offer Competitive salary, extensive benefits, flexible working culture, and opportunities for professional growth. Join a global organization committed to making a difference, guided by our core values : Integrity, Intensity, Innovation, and Involvement.Apply today at jobs.Thermofisher.Com .Thermo Fisher Scientific is an equal opportunity employer committed to diversity and inclusion. J-18808-Ljbffr #J-18808-Ljbffr

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. Discover Impactful Work : The (Associate) Medical Director will provide medical support and medical advice for clinical trials and safety evaluation within the Pharmacovigilance department. A day in the Life : • Provide medical leadership to the study teams, including creating clinical trial protocols while implementing the latest scientific information, contribute to site selection, involved in review and approval of study protocols and amendments, Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), protocol deviation decisions and other clinical documents as required for the conduct of clinical trials., • Real-time Medical Monitoring of clinical studies: ensure medical validity of each individual primary endpoint as well as study subject safety, while ensuring medical issues are identified early. Proactively address customer concerns and correct issues in consultation with the Global Medical Indication Lead., • During initial review of protocols, consult with internal groups and support staff regarding procedural and budgetary items and the necessity for change due to any subsequent protocol amendments. Acquire commitment from other functions to close gaps and address issues timely and effectively. Serve as the chief liaison between the sponsor and all PPD, part of Thermo Fisher Scientific internal departments performing the required tasks during all study phases. Educate Investigator sites by delivering protocol-specific lab procedures presentations and demonstrations during investigator meetings. Manage day-to-day activities during the clinical trial to resolve issues and answer queries., • Act as the medical point of contact for all internal and external stakeholders: interact with investigators as needed, answer questions from IRBs and Health Authorities, prepare and present material to the study executive and independent safety committee if applicable; provide medical training to site staff at Investigator meetings; train CRAs in new indications., • Ensure study compliance for all medical aspects by understanding and applying all relevant SOPs and GCP., • Significant experience within the pharmaceutical industry, clinical trials, and pharmaceutical medicine is critically important., • Fluent in spoken and written English., • Understanding and experience with NDA submission process., • Knowledge of regulatory guidelines for adverse event reporting. Thermo Fisher Scientific is an EEO / Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. #J-18808-Ljbffr