Specialist Consultants
in the Medical Devices Sector

Actualmente estoy buscando a un Área Mánager para una compañía consolidada en IVD en el territorio nacional.

Como responsable de la área y con productos de calidad que reforzarán tu reputación con los clientes establecidos y por hacer serás el encargado de hacer una venta totalmente científica y asesorativa en la que podrás dinamizar tu perfil y adquirir un skillset muy relevante para tu futuro profesional

Siendo una de las compañías líderes a nivel mundial en el sector del diagnóstico tendrás la oportunidad de trabajar con los mejores profesionales del sector y beneficiarte de un excelente crecimiento profesional.

La persona ideal para el puesto debe tener: Minimo de 2 años de experiencia como Product Specialist/ Ventas, idealmente en Cataluña y con productos de Genetica/NGS

• Titulación relevante en ciencias de la salud - PHD seria una ventaja
• Ingles fluido hablado y escrito.
• Disponibilidad para viajar a nivel internacional

Si crees que eres la persona que buscamos y quieres saber mas sobre esta oportunidad, conacta conmigo ahora!

Si esta oportunidad es de su interés, envíe su CV (en formato Word) a Aitor Melia a la siguiente dirección de correo electrónico: [email protected]

Debido al alto número de postulaciones recibidas a diario, pido disculpas por adelantado al no poder garantizar una respuesta a todos los candidatos. Tenga en cuenta que, al estar especializado en el reclutamiento para puestos de ventas y desarrollo de mercado, soy el punto de contacto para informarse sobre estos puestos en el mercado.
Si esta oferta no le interesa, pero conoce a alguien que estaría interesado en esta oportunidad, no dude en ponerse en contacto conmigo, ya que podría beneficiarse de un vale de Amazon ofrecido como una señal de agradecimiento si el perfil sugerido es contratado por nuestro cliente.

Además, puede visitar nuestro sitio web en http://www.nonstop-devices.com para a más ofertas laborales en la industria.
NonStop es uno de los principales proveedores de atención médica del mundo, con una tasa de crecimiento anual de más del 30%. Somos miembros orgullosos de APSCo, una organización dedicada a la garantía de la calidad de los servicios en el mundo del reclutamiento a nivel mundial. Para tener una idea clara del alcance de nuestros servicios, visite nuestra página web o también mi perfil de LinkedIn: https://www.linkedin.com/in/aitormeliasales/

Perfect chance for someone to move to the UK prior to Brexit and continue your development in a fast growing and developing company.

The company is happy to provide relevant training to the right individual but is looking for someone who is ready to learn and take on the new responsibilities. If you are an experienced manager this would be also a lovely place to work with a close-knit team and a nice green location.

You will be in charge of QA in a Medical Devices company so please make sure you have the following experience prior to applying:

* 2-5 years QA experience within a Medical Devices company
* Experience, ability or willingness to manage teams, you will be able to get the necessary training
* Auditing, QMS and CAPA experience

Very good opportunities for your career so apply now to discuss further!

This role is only open to candidates who are eligible to live and work in Europe so please only apply if you meet the visa requirement.

Please send your CV in the Word format to Oksana Kolesnichenko or recommend this role to someone who is looking for an interesting job opportunity and get rewarded for it: [email protected], Tel No: 02035191775| Int Ext: 3176

Please bear in mind that the company doesn't offer visa sponsorship so please apply only if you are eligible to work in the UK.

NonStop is dedicated to raising the standard of ethical recruitment and comprises a number of brands, each having their own niche sector focus.

A medical device company is seeking a homebased QA/RA Officer. From the comforts of your home, you will be able to add to the quality and ensure the regulatory standards of this multi-national company. Your role will be broad as it involves QA and RA which will help keep you interested in your work. They manufacture niche products which are minimally invasive so there is a need for the products and they can help with improving the quality of life of end users.

Your work will include maintaining QMS, CAPA, technical files, ensuring regulatory vigilance, assessing suppliers, and staff training. As the role includes both QA and RA aspects, you will be a key member of the team in making sure the company adhere to new regulations.

You have:

• 3 years in medical device QA and 2 years in medical device RA
• Knowledge of ISO 13485, MDR, and international standards/regulations
• Experience with technical files and CAPA
• Fluency in English
• Permission to work in the EU

If this sounds like the right opportunity for you please apply here or send your CV to me, Zachary Grossman, on the NonStop Consulting website or my LinkedIn. If this role would be great for someone you know please feel free to forward it to them.

Or, if this does not sound like the right role for you, but you are a Quality Assurance or Regulatory Affairs professional within the Medical Device or Pharma industry, please feel free to get in touch and find out about other relevant opportunities we may have.

Our client has their own development and export of a diverse portfolio of consumer health care products like pharmaceuticals, food supplements and medical devices. They deliver the products internationally but the head quarter is still in Belgium which means you are close to the main decision makers and therefore know about future plans and be able to bring your ideas.

Some products of this pharmaceutical company will be classified as medical devices because of the change in classification according to the MDR and therefore they are looking for a Regulatory Officer who can help them to obtain CE-marking and to become compliant to ISO 13485. The manager will give you space to be independent, but is still close if you have questions.

Profile:

- Bachelor or Master Degree in life sciences or engineering or equivalent by experience

- First experience in Regulatory Affairs or Quality Assurance for the medical device industry

- Good knowledge of ISO 13485

- Fluent level of Dutch and English

This company has flexible working hours and allows some home based work so you can improve your work-life balance. Even better, they have quite a short working week but still give a lot of extra holidays that you can spend with friends or family!

If this job appeals to you please apply here or send your CV to me, Annelies De Baere, on the NonStop Recruitment website. If you are not available but you know someone that would be interested, please forward this to them and help the people in your network.

NonStop is one of the largest and fastest growing specialised life-sciences & Med-tech recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licences for all EU8 countries. Please visit our website for a full list of the niche markets we cover.

In the current crisis, it is probably not easy to find the regulatory job you were looking for and there are maybe also less options available, but do not worry I got an opportunity as Junior Regulatory Officer for a medical device company where you can not only gain more experience in the regulatory field but also have the opportunity to support interesting projects such as MDR and rebranding.

This international medical device company provides better quality devices that are also more cost-efficient so you will support the registration activities to put these devices on the EMEA market. This role is quite operational but because you are involved in projects you need to use your organisational skills to reach the set time-lines. They confirmed that you can start this position immediately so you do not have to wait to develop yourself and will get more financial stability.

Profile:

• Bachelor or Master Degree in Science or equivalent by experience
• First experience in Regulatory Affairs is preferred, if not related experience in the medical device or pharmaceutical industry is also accepted
• Project management skills
• IT savvy
• Fluent level of English

If this job appeals to you please apply here or send your CV to me, Annelies De Baere, on the NonStop Recruitment website or my Linkedin. If you are not available but you know someone that would be interested, please forward this to them and help the people in your network.

NonStop is one of the largest and fastest growing specialised life-sciences & Med-tech recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licences for all EU8 countries. Please visit our website for a full list of the niche markets we cover.

Vous êtes autonome pour déposer des dossiers de marquage CE, et apte à adapter la conformité d'une gamme de dispositifs médicaux au nouveau règlement MDR ?

Je vous propose de prendre les rennes du département Qualité & Réglementaires d'une jeune entreprise Bretonne en plein essor. Vous souhaitez un poste à responsabilité dans une structure à taille humaine, qui vous permettra d'évoluer de manière autonome tout en développant vos compétences ?

Je vous propose de gagner en qualité de vie en intégrant cette entreprise en plein essor qui vous donnera l'occasion de travailler en équipe et de vous impliquer dans un projet ayant du sens et un réel intérêt pour la qualité de soin des patients.

En tant que Responsable Qualité & Affaires Règlementaires, vos missions seront les suivantes :

- Préparer et rédiger les dossiers techniques, et vous assurer de leur conformité avec la nouvelle réglementation.

- Être l'interlocuteur privilégié des organismes notifiés.

- Planifier le marquage CE et l'enregistrement des produits à l'export.

- Modeler le système qualité du groupe selon les besoins préalablement déterminés.

Si vous êtes :

- Titulaire d'un Bac +5 en Ingénierie ou Affaires Réglementaires.

- Vous avez au minimum 4 ans d'expérience sur un poste similaire.

- Vous maîtrisez l'anglais.

- Vous maîtrisez les normes applicables aux dispositifs médicaux.

- Vous avez des Connaissances en QMS.

Alors lancez-vous ! Donnez un nouveau tournant à votre carrière.

Contactez Hoel Goasguen, recruteur spécialisé en affaires réglementaires

[email protected] ou au 01.76.75.33.40 +extension 3210

Si vous ne faites malheureusement pas partie des chanceux qui peuvent prétendre à cette opportunité, parlez-en autour de vous !