OFERTAS PARA LIDERAR
TU CARRERA PROFESIONAL
OFERTAS PARA LIDERAR
TU CARRERA PROFESIONAL

Tu éxito, nuestro objetivo.

Encuentra y desarrolla tu talento en las mejores empresas biomédicas de referencia.

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Confidencialidad y Ética con nuestros clientes y candidatos. Eficiencia en los procesos. Es el momento de contar con expertos que te ayuden a encontrar tu siguiente reto profesional. Es tú momento. ¿Empezamos?

DIVERSIFÍCATE Y APROVECHA TUS SKILLS

Formar parte de la base de datos de LIM Global es sumarse a una red global especialista en Life Sciences. Para encontrar un ambiente de trabajo que crea en tu talento. Para conectar los mejores profesionales con empresas extraordinarias. Pasión. Respeto. Confianza. Integridad. Súmate a nosotros.


Nuestras búsquedas tienen en cuenta las características y habilidades de cada candidato. Contamos con más de 20 años de experiencia en encontrar el engranaje perfecto de las necesidades de nuestros candidatos y sus trayectorias profesionales con las estrategias y culturas corporativas de nuestros clientes.

Regional Account Manager
MAD
Madrid

Regional Access Manager Spain

Our client is a successful and fast-growing international specialty pharma company. The corporation has grown into a renowned specialist for rare diseases, intensive care and emergency medicine with the goal to become one of the leading players in their area of expertise in Europe.

To support their successful, fast-growing team the company is now looking for a Regional Access Manager who plays a key part in increasing and maintaining the organization’s customer engagement, building strategic relationships with payers and related market access stakeholders at a regional and local level.

Responsibilities:

  • Define and implement Market Access strategies and tactics for access and retention of the company products at regional level demonstrating their therapeutic, economic and societal value using a deep knowledge of the regional environment.
  • Elaborate and implement Regional Market Access Plans in the main geographical areas for new products as well as for the existing portfolio aligned with the Company Strategy.
  • Identify, map, and prioritize key regional, hospital and local stakeholders and relevant decision makers to ensure timely access to the product.
  • Establish relationships with key stakeholders such as Regional Health Authorities, Medical Societies, Scientific Institutions, Payers and Patient Advocacy groups.
  • Build a solid network of effective and trustful relationships with key accounts/hospitals/decision makers.
  • Provide inputs into the development and support of the product strategy and contribute to develop the appropriate tools for the delivery of the brand value messages to market access stakeholders.
  • Identify and drive projects and collaborations with access stakeholders that improve health outcomes and foster brand awareness.
  • Manage and Coordinate Regional Market Access activities and ensure the alignment with the Company Strategy.
  • Analyze local access issues and opportunities, anticipating changes in the local healthcare landscape.
  • Work collaboratively with the full cross-functional team.
  • Active collaboration and alignment with Sales, Marketing and Medical Affairs operations to ensure the implementation of these plans to the regional markets in full respect of Health Policies, regional laws, rules and guidelines.

 Experience & Qualifications:

  •  Bachelor’s degree in Life Sciences (Pharmacy, Medicine, Biology…) or Economics. MBA, MA & HEOR postgraduate training is highly preferred.
  • 3-5 years of experience as Regional Market Access (RAM).
  • Strong interpersonal skills to build and maintain strong relationships both internally and externally.
  • Experience in strategic planning/contributing to a national business strategy.
  • Strong influencing and negotiation skills, as well as strategic vision.
  • Deep knowledge and understanding of formulary processes, regional and local tenders, and financial drivers.
  • Strong interpersonal skills and ability to operate within numerous networks.
  • Able to work across different levels & types of customer groups to engage key decision makers.
  • Must be able to credibly discuss pharmaceutical product details and be able to synthesize clinical and economic evidence into clear and direct messages with all level stakeholders.
  • Experience in negotiations with regional health authorities and hospital management is preferred.
APPLY
GMP Manufacturing Manager
BIO
Bilbao

A new state-of-the-art, Advanced Therapies Contract Development and Manufacturing Organization (CDMO), located in Bilbao, Spain, is looking for a GMP Manufacturing
Manager.


Key duties /Responsibilities:

  • Manage, develop, and lead a team of skilled professionals.
  • Manage the GMP manufacturing facility to meet established delivery schedules and the company's stringent quality standards.
  • Support a culture of operational excellence where teamwork and active problem solving lead to continuous improvement throughout the organization.
  • Ensure that team activities, equipment, facilities, and personnel are operated and maintained in a state of compliance with appropriate requirements.
  • Defend his/her area of responsibility in regulatory or customer audits.

Minimum Qualifications:

  • University degree.
  • 8-10 years of experience in a pharmaceutical/biotechnology GMP environment.
  • 3+ years of experience supervising a team in a bio/pharmaceutical cGMP operating environment.
  • Expertise in one or more of the following areas: chromatography (ÄKTA process systems), tangential flow filtration or sterile filtration.
  • Experience in commercial scale cGMP operations, deviation handling, GMP change control and validation.
  • Familiarity with advanced therapy products is a plus.
  • Experience in defending and managing audits, including those conducted by regulatory agencies such as EMA and FDA, as well as customer-initiated audits.
  • Flexible enough to adapt to a growing organization and diverse client needs.
  • Proven ability to innovate and drive continuous improvement.
  • Ability to build and lead high performing teams and be a strong team player.
  • Strong organizational skills.
  • Ability to solve practical problems and deal with a variety of variables.
  • Good communication skills.
  • Fluent in English and Spanish.

We offer:

  • Join a new CDMO with a unique, disruptive technology in a high-growth market.
  • Help build a high-performance organization.
  • Initiate and optimize GMP manufacturing activities.
APPLY
Drug Discovery Director
PNA
Pamplona

Cima is a translational research institute of the University of Navarra, based in Pamplona, Spain.
Selected candidate would lead a team, with the goal to discover new molecules, against novel targets or mechanisms of action discovered by Cima, to become therapeutic agents that might
address unmet medical needs.

Main Responsibilities:

  • Participate in the Steering Committee, responsible for the internal scouting process to identify projects with small molecules, with potential for early development and
    optimization.
  • Coordinate the full drug discovery process, once a new target or mechanism of action has been discovered, until a new family of molecules has been patented.
  • Confirmation of the validity, in vitro and in vivo, in terms of efficacy and safety of the new molecules and targets or mechanisms of action of clinical interest.
  • The selected professional will be directly responsible for the design of the families of target molecules.
  • Will participate in the coordination of all the teams and tasks involved in the drug discovery process, such as:
    a. Obtaining and expressing target proteins.
    b. Biochemical and biophysical assays between targets and ligands.
    c. Design of the families of molecules.
    d. Computational studies, including studies with artificial intelligence.
    e. Supervision of the CRO in charge of the synthesis of molecules.
    f. Management of all regulatory preclinical, PK-PD, ADMET studies.
    g. IP coordination.
  • Lead the drug design process.

Required Qualifications & Experience:

  • Participate in the BD and IP committees.
  • Ph.D. in chemistry or pharmacy with postdoctoral training in medicinal chemistry.
  • 10+ years of drug discovery experience.
  • 6+ years of drug design experience and should have detailed knowledge of the drug discovery process.
  • Additional experience in computational and AI studies will be an asset.
  • Track record of patented molecules.
  • Ability to work cross-functionally with a variety of departments, functions and stakeholders.
  • Strong persuasion and negotiation skills.
  • Effective communication of project status, science, and strategy to a variety of internal and external audiences.
  • Fluency in English is a must, Spanish is preferred.
APPLY
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+20
AÑOS DE EXPERIENCIA
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Y UNA RED DE PROFESIONAL
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