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LESVI job offers

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As part of Neuraxpharm, Lesvi 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 experience, 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 equipped to achieve each milestone we set.

We offer a compensation package that, besides a competitive salary, also includes company benefits
and policies designed to foster a healthy work/life balance.

What we are looking for

The Groups's current growth and international expansion, 
is encouraging us to continuously search for new talent.

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

...Neuraxpharm is counting on you!

Pharma job openings

JOB OPENINGS

Talent acquisition

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

Our current job opportunities are:

# 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




# 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



# 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).




# OPERARIO/A 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 un candidato/a 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).




Send us your CV

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

  • Basic information about Data Protection

  • Entity responsible

  • LABORATORIOS LESVI S.L., under registration number B-08165789, 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.

  • Legal grounds

  • Consent of the interested candidate.

  • Recipients

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

  • Rights

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

  • Additional information

  • You can consult the additional and detailed information concerning Data Protection contained within our Privacy Policy via our website https://www.lesvi.com/privacy-policy