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Work at Neuraxpharm

JOIN US

Neuraxpharm is composed of a specialised and motivated team who share values such as creativity and innovation, integrity, solidarity, engagement and team work. 


Because people and products are the cornerstones of our business, we promote innovation through talent acquisition practices that ensure diversity and inclusion. This enables us to develop new ideas through the multiple and diverse ways of thinking of employees from different cultures, with different backgrounds and experiences, who share their unique perspectives in different areas of the business.

What we offer

Our team of professionals is our main strength.

We have a policy of continuous training and professional development which contributes to
the integration of our company and guarantees our employees are prepared to achieve each milestone we set.

We offer a compensation package that, besides a competitive salary, also includes company benefits
and policies designed to make personal and professional lives compatible.

What we are looking for

Neuraxpharm's current situation, in a growth and international expansion stage, 
encourages us to continuously search for new talent.

If you believe that you share our values, if you are interested in joining a company with professional development opportunities...

...Neuraxpharm is counting on you!

Neuraxpharm work

JOB OPENINGS

Talent acquisitions

To join Neuraxpharm means entering a competitive working environment full of goals. Our employees share values such as results orientation, client orientation, teamwork, cooperation and a positive attitude towards continuous learning.

Our current job opportunities are:

# Neuraxpharm Germany: QUALIFIED PERSON


Reporting to the QA Manager, Qualified Person role will act as deputy of the QP to ensure straight through product flow and the team meets all product quality and compliance requirements to enable disposition for each batch. This requires the management of a robust Quality Management System to support a flexible, collaborate, multi-skilled teamwork environment, providing quality support, guidance and expertise on all Quality Assurance and cGMP compliance aspects to ensure the success of transference will be done.

Primary activities/responsibilities as QP deputy:

 Review and approve master batch manufacturing records as well as Annual Product Quality Reviews
 Participation in investigation on critical complaints
 Review quality agreements, change controls and process validation protocols
 Participation in the execution of risk assessments, audits and inspections. Implementation of GMP training courses
 Participate and Comply with the company Quality Management System (QMS) requirements, including ownership as required

We require:

• Bachelor’s Degree in Pharmacy
• +2 years’ experience in Quality Control in a pharmaceutical laboratory 
• Key Competencies: Analytical thinking, Problem solving, Results Driven, Management Skills, Partnership and Cross-functional team leadership
• Fluent and professional German is a must (other languages are valued)
• Location: Langenfeld (Düsseldorf area)

We offer:

• Individual Professional development in a leading European pharmaceutical company with an ambitious international growth strategy
• Permanent contract and Company Benefits

All interested candidates meeting the above requirements should send their CVs quoting the reference “QP”, either by email to: i.daubenbuechel@neuraxpharm.de


Apply now

# Laboratorios Lesvi: TÉCNICO DE DESARROLLO CLÍNICO


En dependencia del Jefe de Desarrollo Clínico, se encargará de la evaluación, diseño, selección de CROs y seguimiento de los estudios clínicos (Fase I.- Bioequivalencias). Al mismo tiempo, se encargará de mantener y revisar archivos de los diferentes estudios, preparar módulos 2 y 5 del dossier de registro y contestar cartas de deficiencias.

Precisamos:
 
  • Licenciado/a Ciencias de la Salud (Farmacia, Biología, Medicina) valorándose formación complementaria de Posgrado en Ensayos Clínicos.
  • Experiencia mínima demostrable en el puesto de 3-5 años, siendo su procedencia de CRO o bien de la industria farmacéutica.
  • Profesional organizado/a, planificado/a, resolutivo/a, con capacidad negociadora, con marcado espíritu de equipo y habilidad para las relaciones interpersonales.
  • Dominio del idioma inglés, ser experto/a usuario/a del software informático habitual, así como conocimientos en otras aplicaciones informáticas.
  • Disponibilidad para viajar.

Ofrecemos:
 
  • Incorporación a un sólido grupo farmacéutico internacional y, a un equipo de I+D dedicado al desarrollo de medicamentos genéricos, con responsabilidades sobre productos y, todas las actividades regulatorias relacionadas con el producto, tanto a nivel internacional como nacional.
  • Formación continuada a cargo de la compañía.
  • Retribución económica en función de la experiencia y valía aportada.
 

Apply now

# Laboratorios Lesvi: CLINICAL SENIOR SCIENTIFIC COORDINATOR



Reporting to the Corporate Clinic Director, will be responsible for coordinating and leading the projects of the company. Being their duties:
 
  • Designing, planning and management Clinical Research projects; determining the resources (including costs, timeliness, general resources) required to complete and objectives and measures upon which CRO’s projects. Develop a schedule for project completion that effectively allocates the resources to the activities.
  • Lead and execute the project according to the project plan. Monitor the progress of the project and adjust as necessary to ensure the successful completion of the project.
  • Analyze, measure and report the results of the department and new proposal (elaborating writing and final project following presentation, technical reports, proposals, SOPs and documentation for IP and FDA filling).

We require:
 
  • Degree in Pharmacy and Master’s/ Postgraduate specialist in Clinical Research.
  • +5 years professional work experience as CRA Senior in pharmaceutical, experience in managing CRA team, project planning and control senior professional is required.
  • Ability to work independently and represent sound strategies is required.
  • Professional with skills as an organization, negotiation and conflict management, independent, cooperative, results oriented, initiative and critical thinking, consistent, training experience and ability for teamwork.
  • Job requires knowledge of the drug development process, being competent in Biopharmaceutics, Pharmacokinetic and Formulation support. Cross-functional and global project team leadership experience preferred.
  • Proficient technology skills (e.g., MS Office software, MS Project, etc.) required.
  • Fluent English/Spanish. Knowledge of other European languages (German, French…) will be valuable.
  • 10% Availability to travel.
 
We offer:
 
  • Join a solid chemical pharmaceutical group specialized in generic medicines, in a growth and international expansion stage.
  • Permanent contract and Company Benefits.
  • Economic conditions will be according to the experience and skills provided.
  • Continues training program.
 
All interested candidates meeting the above requirements should send their CVs quoting the reference “CRA_C”, either by email to: ecosta@neuraxpham.com




Apply now

Send us your cv

If you would like to join the Neuraxpharm team, you can send your CV to jobopening@neuraxpharm.com, indicating the position you would like to fill, or you can fill in the following form:

  • Basic information about Data Protection

  • Entity responsible

  • NEURAXPHARM HOLDCO IBERIA S.L.U. (NEURAXPHARM), under registration number B-87459624, address: Avda. Barcelona, 69, 08970 Sant Joan Despí, Barcelona, Spain Telephone +34 934 759 600 - Email: jobopening@neuraxpharm.com

  • Purpose

  • Processing your application for selection processes.

  • Legitimation

  • Consent of the interested candidate.

  • Recipients

  • Other companies of NEURAXPHARM (neuraxpharm Arzneimittel GmbH, Neuraxpharm Italy S.p.A., Neuraxpharm France S.A.S., Qualigen S.L., Laboratorios Lesvi S.L. and Inke S.A.)

  • Rights

  • Access, rectification, deletion and other rights detailed in the additional information.

  • Additional information

  • You can consult the additional and detailed information on Data Protection in the Privacy Policy of our website http://www.neuraxpharm.com/privacy-policy