Life Sciences & Healthcare

Our Expertise

At Antal, we have specialist recruiters around the world that can support your career or business within the Life Sciences & Healthcare industry.

Our teams of experts work across a variety of roles, providing the highest quality recruitment services for business’s in Medical Devices, Pharmaceuticals and Cosmetics – among other areas in Life Sciences & Healthcare.

If you are a candidate, find jobs in Life Sciences & Healthcare using our Job Search and discover the next step in your career.

We also work across various disciplines, so if you’re a professional in Sales, IT, Accounting, Engineering, Operations or any other discipline, you may find the perfect position for you across any of our eight industries on our job board.

If you’re a client, you can use our Office Search to find an Antal Office that can provide you with the best available talent for your business. Our services include RPO Consultancy, Permanent, Contract and Executive Recruitment.

 

 

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Regional Sales Manager:

Antal selecciona : Sales Manager Un@ responsable de ventas que estará a cargo del desarrollo de negocio en la zona asignada (Castilla y León y Galicia Gracias por contactar con ANTAL

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Technical Project Manager - South Milan

Technical Project Manager - South Milan

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Directeur R&D Dispositifs Médicaux

Vous êtes un Directeur R&D créatif dans le secteur de la Santé / des Dispositifs Médicaux, orienté Business Development, possédez un savoir-faire en matière de normes relatives aux DM, des compétences en leadership, Rejoignez B.Braun en qualité de Directeur R&D sur son site de Poitiers - Cadre de vie agréable – Excellentes conditions de travail.

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QA Compliance Specialist

£40000.00 - £45000.00 per annum

IT Compliance Analyst - fixed term 12 month contract opportunity, working for a global Pharma organisation who offers competitive salary and excellent benefits.Quality Assurance Develop and maintain the quality management system to assure compliance with GMP and GDPPlan, implement and perform internal quality auditsMonitor and report on product non-conformitiesManage and maintain systems for change control, deviation and CAPAManage and maintain a system for product complaint handling ensuring timely completion and reporting. If necessary, assist in any product recallCollect, collate and compile data for periodic product quality reviews, including preparation of reportsAssist in conducting external/supplier audits as requiredReview batch release documentation and coordinate correction of any errorsAssist in maintaining the system for document control, so that the current local and regional SOP systems are managed both in hard copy and electronicallyMaintain documentation archiving systemsPrepare and maintain GMP documentation such as standard operating proceduresConduct training sessions on QA systems as requiredContribute to Global Quality goals, projects and initiativesProcessing of Product Returns forms including usage decisionQuality Control Provide support in the planning and scheduling of laboratory testingInitiate follow-up action on out of specification materialsLiaise with contractors and the laboratory on sample quantities and sampling frequencyEnsure stability testing is performed in accordance with the requirements of the marketing authorisationsRegulatory Provide support and advice relating to the manufacturing and technical content of the Company's product licences and submissionsEnsure that the requirements and conditions of the Company's product licences and submissions are reflected in the manufacturing, technical, and testing processes and procedures. Parkside Recruitment Ltd is acting as an Employment Business in relation to this vacancy. Parkside Recruitment is an Equal Opportunities Employer.

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Gerente de Investigación Medica

25,000

Conocimientos en: Investigación y en Monitoreo Clínico. Manejo de las Buenas Prácticas Clínicas. Conocimientos Amplios en Farmacovigilancia. Manejo de Guías ICH. Manejo de Bioestadística. Manejo de Base de Datos. Manejo de Personal. Normatividad Local e Internacional. Amplio conocimiento en la Metodología de la Investigación en ensayos clínicos. Administración de recursos financieros de los proyectos a su cargo. Manejo de Proyectos. Implementación de "Plan de Manejo de Riesgos" en Investigación Clínica. Preparación e Implementación de Auditorias a los Proyectos a su cargo. Supervisión de la Calidad de Estudios Clínicos en la Investigación Clínica.

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Representante Médico

Licenciatura a fín a odontología o áreas médicas (concluida o trunca). Contar con disponibilidad de horario y de viaje (INDISPENSABLE). Excelente presentación y excelente actitud. Contar con automóvil propio en buenas condiciones (INDISPENSABLE). CON o SIN experiencia. Conocimiento en el manejo de auditorías (deseable). Indispensable vivir en la Ciudad de México. Contar con conocimientos en AUDITH FARMA, prescripta, reporte de visita médica, análisis ATV, IMS,y conocimiento del mercado (deseable).

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Jefe de Proyecto

Salario Competitivo

• Planear, coordinar y expeditar las tareas necesarias para el desarrollo y lanzamiento de nuevos productos. • Definir y controlar el presupuesto requerido para el desarrollo y lanzamiento de nuevos productos. • Acordar con las Direcciones involucradas la asignación de recursos de sus áreas para integrar los equipos de trabajo necesarios para el desarrollo y lanzamiento de nuevos productos. • Apoyar en el establecimiento de herramientas y cultura de gestión de proyectos.

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Market Access

110,000MXN + PSL

Market Access Manager

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Gerente de Distrito

30,000 + Comm + PSL

Gerente de Distrito

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Associate Director, Public Affairs

Car allowance plus stock

Our client is a bio-pharmaceutical company with therapeutic in HIV/AIDS, liver diseases, cancer and inflammation.They are looking for an Associate Director to deliver strategic branded and unbranded communication programs and patient advocacy engagement as it enters rheumatology. The role reports in to the US and works closely with cross-functional and Public Affairs colleagues at the global and country levels.Job duties include:Setting the communications strategy for markets outside of the US.Shaping the product launch communications and advocacy engagement plans.Working in partnership to drive alignment across company communicationsCommunicating data and regulatory milestonesDesigning and implementing disease awarenessDeveloping compelling materials to support external communications, including key messages, Q&A documents, press releases, presentations, videos, social media content, etc.Responding to media requests and coordinating interviews with spokespeople and opinion leader spokespeople, as appropriateDeveloping/strengthening relationships with a wide variety of community advocates, media and other influential organisationsContinuously scanning the environments to proactively identify and manage issuesCoordinating with cross-functional colleagues to ensure alignment and collaboration in strategic priorities and messaging across different stakeholdersManaging agency partners Knowledge, Experience and SkillsGlobal or pan-EU experience in product PR, media and advocacy within the pharmaceutical sectorDemonstrated experience in media relations (traditional and social), issues management; knowledge of healthcare and industry media and reporting trendsExperience of working within the inflammation therapy area is highly desired but not essentialExperience managing multiple projects (timelines, budgets, priorities) simultaneously; flexibility and results-oriented focus are essentialAbility to interact with senior management and high-profile experts appropriately, with confidence and easeAbility to understand and accurately communicate complex scienceAbility to give formal presentations to internal and external audiences of various sizesExperience working successfully with patient organisationsParkside Recruitment Ltd is acting as an Employment Agency in relation to this vacancy. Parkside Recruitment is an Equal Opportunities Employer.

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