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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:

# BUSINESS DEVELOPMENT MANAGER

Reporting to the Head of Business Development and Licensing, this position will be responsible for the in-licensing activities of the new products for Neuraxpharm to cover specific and local needs as well as for the Neuraxpharm Group at European level.

Key responsibilities and tasks:
  • Prospection potential suppliers, negotiate external counterparts to execute agreements and monitoring the correct accomplishment of the agreed terms in the established agreements.
  • Achieve the licensing objectives fixed by local affiliates and the Group within the period and planned budget, in order to fulfill the agreed MRP.
  • Optimization of the exiting agreements with the objective of getting better supply conditions and facilitating the harmonization of the supplies within the Group.
  • Identification of new business opportunities for Neuraxpharm.
  • Maximizing the “network” of relation with others companies in the sector, (suppliers, Company Clients, etc..)
  • Share and discuss information as a part of a BD team and collaborate closely with different departments (RA, MKT, Q, Provisioning, Planning and Sales) to guarantee the launch of the product in the right time and correct commercialization.
  • Represents the company in the different forums and events related with the business development.


We require:
 
  • Bachelor’s in Science Degree (Pharmacy, Chemistry, Medicine or similar) and Master in Economics would be valuable.
  • +5 years professional work experience in Licensing in with wide experience Pharmaceutical International Company.
  • Proficient in identifying business opportunities, technical pipeline analysis and benchmark pharmaceutical, Regulatory Affairs, Marketing and Sales knowledge..
  • Senior profile, self-started, motivated, high developed problem-solving skills, diligent, thorough and flexible. He/she should be capable of challenging in a constructive and positive manner, able to listen and influence, pragmatic, adaptable and comfortable with change. Ability for team work and communication skills.
  • Fluent English/Spanish.
 
 
We offer:
 
  • Join a solid chemical pharmaceutical group specialized in generic medicines, which is expanding internationally.
  • Individual professional training for developing his/her professional career.
  • Permanent contract and company benefits.
  • Economic conditions will be according to the experience and skills provided.
  • Ability to travel (30%).
 
All interested candidates meeting the above requirements should send their CVs quoting the reference “ BDM”, by email to: ecosta@neuraxpharm.com



Apply now

# HEAD OF MERGERS AND ACQUISITIONS NEURAXPHARM



Reporting to the Chief Business Development Officer of Neuraxpharm Group, this role is responsible to evaluate and lead potential merger and acquisition projects for the all the Companies and/or products. Leading the inorganic growth of the group in alignment with the overall Business Development strategy. Consequently, he/she will coordinate the corporate and local functions in due diligence activities defining the appropriate framework, evaluation models and timelines to execute the growth strategy.

 
Main responsibilities:
  • Coordinate with Finance team the business case for each potential project
  • Collect and align with the different resources the information needed to fully evaluate the project
  • Refine business cases for stakeholder’s decision making
  • Lead (with no direct mandate) the functions defining clear timelines and responsibilities to ensure execution
  • Establish and strengthen the connection with investment banking and other sources of M&A projects and liaison with the Finance function
  • Liaise with the Country Managers and Group functions in order to ensure the right execution of M&A projects in time and in full

We require:
  • Bachelor’s degree in Economic or similar background.
  • +3 -5 years’ experience in investment and evaluation/consulting context.
  • Life Science or pharmaceutical experience is desirable.
  • Good understanding of corporate investment and due diligence processes.
  • Key Competencies: Cross-functional team leadership is a must as is the ability to lead as project manager within a complex business environment with multiple stakeholders.
  • Fluent and professional English is a must (other languages are valued).
  • Location: Spain (Barcelona area) or Germany (Düsserdolf area).
We offer:
  • Individual professional development in a leading European pharmaceutical company with an ambitious international growth strategy.
  • Permanent contract and Company Benefits.
  • Economic conditions will be according to the experience and skills provided.
 All interested candidates meeting the above requirements should send their CVs quoting the reference “ M&A” by email to ecosta@neuraxpharm.com



Apply now

# Laboratorios Lesvi: TECNICO DE LABORATORIO MICROBIOLOGÍA

En dependencia del Jefe de sección de Microbiología, se integrará en el Dpto. de Control de Calidad, encargándose de redactar y supervisar los análisis, así como garantizar el correcto estado de los equipos, instrumentos y reactivos necesarios para realizar los mismos y para asegurar que los resultados obtenidos son válidos y fiables.

Se precisa:
  • Profesional analítico, organizado, sistemático, entusiasta, con elevado espíritu de equipo y habilidad para el trato con personas.
  • Licenciado en Biología o Farmacia y preferiblemente con master especializado en la Industria Farmacéutica / Microbiología, con experiencia como técnico de microbiología en Control de Calidad de una empresa Farmacéutica
  • Amplios conocimientos de técnicas microbiológicas, valorándose experiencia en productos estériles y asépticos.
  • Se valorará inglés, conocimientos de informática a nivel de usuario, demostrar un elevado interés por la gestión de documentación, elaboración de Bases de Datos y conocimientos de sistemas LIMS.
Se ofrece: 
  • Incorporación a un sólido grupo químico-farmacéutico especializado en medicamentos genéricos, en fase de expansión.
  • Se ofrece incorporación inmediata
  • Contrato indefinido.
  • Horario partido-flexible.
  
Aquellas personas interesadas que reúnan los requisitos exigidos deberán enviar su historial profesional actualizado, indicando la referencia Ana. Mirco a: jobopening@neuraxpharm.com.



Apply now

# Laboratorios Lesvi: TECNICO PARA CONTROL DE CALIDAD FISICO-QUÍMICO

En dependencia del Jefe de sección se integrará en el Dpto. de Control de Calidad, encargándose de redactar y actualizar documentación técnica de acuerdo con la normativa vigente. Transferencia, validación y puesta a punto de métodos analíticos. Dar apoyo técnico a los analistas de Control de Calidad y supervisar los análisis, así como garantizar el correcto estado de los equipos, instrumentos y reactivos necesarios para realizar los mismos y asegurar que los resultados obtenidos son válidos y fiables.


Se precisa:
 
  • Profesional analítico, organizado, sistemático, entusiasta, con elevado espíritu de equipo y habilidad para el trato con personas.
  • Licenciado en Ciencias Químicas o Farmacia y con Master especializado en la Industria Farmacéutica o en Técnicas analistas, con experiencia más de 5 años en el uso de técnicas analistas químico-habituales (HPLC, GC, espectroscópicas).
  • Imprescindible inglés, conocimientos de informática a nivel usuario, demostrar un elevado interés por la gestión de documentación, elaboración Bases de Datos y conocimientos de sistemas LIMS

Se ofrece:
 
  • Incorporación a un sólido grupo químico-farmacéutico especializado en medicamentos genéricos, en fase de expansión.
  • Retribución económica en función de la experiencia y competencias aportadas.
  • Contrato indefinido.
  • Horario partido-flexible.
 
Aquellas personas interesadas que reúnan los requisitos exigidos deberán enviar su historial profesional actualizado, indicando la referencia Tec.Control a: jobopening@neuraxpharm.com.



Apply now

# Laboratorios Lesvi: QA MANAGER and QP (QUALITY PERSON)


Based in Sant Joan Despí, the QA MANAGER Qualified Person will be accountable 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.

QA MANAGER will be an active member within the cross functional Team providing independent quality support, guidance and expertise on all Quality Assurance and cGMP compliance aspects to ensure the success of transference will be done. QP will model the company's leadership behaviors and understand the production principles to drive a culture of continuous improvement building a High-Performance Organization.

Primary activities/responsibilities:
  • IMPROVE AND MAINTAIN Quality Standards: Identifies and resolves problems performs audit, determines systems improvements, define KPI’s and implements change.
  • Meets Quality Assurance Financial Objective by estimating requirements: preparing an annual budget; scheduling and controlling the cost and initiating corrective actions.
  • Manage and Develop a Senior Quality Assurance Team.
  • Develops Quality Assurance Plans by conducting risk analyses: Identifying critical control points and preventive measures, establishing critical limits and monitoring procedures, corrective actions and verification procedures.
  • Validates Quality Process by establishing products specialization and quality attributes: measuring production: documenting evidence, determining operational and performance qualification; writing, updating and approving quality assurance procedures; documentation control, calibration plan; supplier qualification.
  • Ensures Compliance to the filed dossier.
  • Maintains and improves product quality by completing products, company and systems audits; investigating customer complaints, collaboration with other members of management to develop new products and engineering designs, and manufacturing and training methods.
  • Prepares quality documentation and reports by collecting, evaluating and summarizing information and trends including failed processes, stability and organization reputation by accepting ownership for accomplishing new and different requests: exploring opportunities to add value to job accomplishment.
  • Qualified Person: Batch release of marketed batches: tach release for clinical trials; psychotropic official declaration: recall; contact with Health Authorities.



Minimum requirements
:

  • Education: University Degree in Pharmacy
  • +3 years of QP experience, ideally in the release of oral solids, capsules, injectables, sterile and BFS pharmaceutical products
  • Qualified Person under the permanent provisions
  • At least 8 - 10 years’ experience in the pharmaceutical industry to include QA/QC experience
  • Problem solving skills - role holder is required to solve technical issues
  • Management skills - role holder has responsibility for coaching and mentoring other Quality staff
  • Auditing experience and lead auditor trained (preferred)
  • GMP’s excellent knowledge will be a must
  • Proficiency in English

We offer:

 

  • Join a solid chemical and 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

 

All interested candidates meeting the above requirements should send their CVs quoting the reference “QA-Manager” by email to: ecosta@neuraxpharm.com


Apply now

# Inke: COMMERCIAL AREA MANAGER APIs (USA)



Please find the job description on our APIs' affiliate website at the following link:

Apply now

# Inke: COMMERCIAL AREA MANAGER APIs (MIDDLE EAST / SOUTHEAST ASIA)



Please find the job description on our APIs' affiliate website at the following link:

Apply now

# SENIOR SAP PROJECT MANAGER



Reporting to the Group IT Manager, this position will be as a leader the implementation project for the Group and roll-out across Europe: Italy, France, Czech Republic, Hungary, Poland, Slovakia... He/she will be responsible for designing, developing and implementation SAP and IT tools, processes, developing, trainings across the several affiliates in the Company during the group expansion and growth.

Key responsibilities and tasks:
  • Primary focus on leading implementation SAP project and roll-out in the new companies of the group (define, follow and supervise the consultant implementation in each country)
  • Processing, reviewing of information and monitoring of the activities to be carried out by the external consultancy that carries out the implementation
  • First level of company SAP integration Help Desk is a part of this role and support new key users
  • The ability to define needs and conduct on training, reviewing manuals documentation
  • Assist in systems and process improvement projects
  • Assist in the development and implementation of new SAP policies within the Group
  • She/he will be integrated in the IT team and will have close collaboration with internal and external company SAP team

We require: 

  • Bachelor’s Degree in Engineering, in Computer Science, IT or equivalent
  • +5 years professional work experience in Big Four Company’s as Senior Consultant with wide experience in SAP integration in several companies or a corporate SAP Project Manager in an international company
  • Proficient in SAP (SAP SD-MM Expert in Material Management. Experience implementation: Sales/Purchase Order Management, Sales/Purchase Master data Management, Delivery Order Management, Complaint and returns, Billing, Pricing, COPA integration with SD (Account determination), SD/FI MM/FI Integration and Sales Purchase Organization structure) are required
  • Pharmaceutical sector and reporting tools would be valuable
  • Senior profile, self-started, motivated, high developed problem-solving skills, diligent, thorough and flexible. He/She should be capable of challenging in a constructive and positive manner, able to listen and influence, pragmatic, adaptable and comfortable with change. Ability for team work and communication skills
  • Fluent English/Spanish
  

We offer: 

  • Join a solid chemical pharmaceutical group specialized in generic medicines, which is expanding internationally
  • Individual professional training for developing his/her professional career
  • Permanent contract and Company Benefits
  • Economic conditions will be according to the experience and skills provided
  • Base located in in our offices at Invent Farma (Barcelona, Spain)
  • Ability to travel (+30%)

 

All interested candidates meeting the above requirements should send their CVs quoting the reference “ SAP PM”, either by email to: ecosta@neuraxpham.com or by fax at +34 93 373 60 67.



Apply now

# 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

# Laboratorios Lesvi: OPERARIAS DE ENVASADO (Turno intensivo tarde) Temporal 6 meses



En dependencia del encargado de turno, se integrará en un equipo llevando a cabo las principales tareas de la sección de envasado, en el Departamento de Producción. 

Su cometido se centrará principalmente en el trabajo en maquinas automáticas: emblistadora, stocar, encartonadora…


Buscamos candidatas con:


• Formación de Ciclo Formativo de Grado Superior en Fabricación de Productos Farmacéuticos, Análisis y Control, FPI o II Química o similar. (No se descartarán candidaturas por formación)
• Experiencia demostrable entre 3 y 5 años en la fabricación y/o envasado de productos farmacéuticos

Ofrecemos:

• Incorporación inmediata a un sólido grupo químico-farmacéutico especializado en medicamentos genéricos, en fase de expansión
• Formación continuada a cargo de la Compañía
• Contrato: temporal de 6 meses


Aquellas personas interesadas que reúnan los requisitos exigidos deberán enviar su historial profesional actualizado, indicando la referencia: 
"O. Envasado" jobopening@neuraxpharm.com o bien a Neuraxpharm Holdco Iberia, S.L.U., Avda. Barcelona 69, 08970 Sant Joan Despí (Barcelona).


Apply now

# Laboratorios Lesvi: OPERARIO/A FABRICACIÓN DE SÓLIDOS (Turno tarde/noche - contrato 1 año)


En dependencia del Encargado de turno, se integrará en un equipo llevando a cabo las principales tareas de realizar mezclas, compresión, estuchado y control de proceso de las formas sólidas, de acuerdo con las Guías de Fabricación y instrucciones del departamento.


Buscamos candidatos/as con:

• Formación de Ciclo formativo de Grado Superior en Fabricación de Productos Farmacéuticos

• Personas con experiencia mínima de dos años en fabricación de formas sólidas, con experiencia en maquinaria de Sólidos en mezclas, granulación y compresión (lecho fluido, granuladora, máquinas de comprimir, dosificadora de cápsulas y/o bombos de recubrimiento) del sector farmacéutico


Ofrecemos:

• Incorporación inmediata a un sólido grupo químico-farmacéutico especializado en medicamentos genéricos, en fase de expansión

• Retribución económica en función de la experiencia y competencias aportadas

• Horario intensivo tarde/noche. Contrato: 1 año



Aquellas personas interesadas que reúnan los requisitos exigidos deberán enviar su Curriculum Vitae, indicando la referencia "Operario Sólidos" a: jobopening@neuraxpharm.com o bien a Neuraxpharm Holdco Iberia, S.L.U., Avda. Barcelona 69, 08970 Sant Joan Despí (Barcelona).


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:

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  • 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

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  • 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.)

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