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Work at Neuraxpharm


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


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): PATENT ADVISOR

Reporting directly to the IP Manager, he/she will be responsible for providing IP opinion and legal advice on Neuraxpharm’s products to the project members to ensure freedom to operate and protection of Neuraxpharm’s intellectual property rights.

IP specialist main duties will imply the drafting and prosecution of patent applications, providing patent infringement risk opinions, technical and legal expert advice to the company.

We require:

  • BSc/ MSc/ PhD in Chemistry or Pharmacy or similar.
  • Specific technical knowledge in Patents. It will be significantly valued to have the qualification of "European Patent Attorney"
  • +3 years’ experience as an Intellectual Property senior team member in the Pharmaceutical Industry.
  • Proven experience in drawing/filing patents and elaborating patentability and infringement patent reports, searching scientific-technical patent data information in professional online databases.
  • Full command of English. Knowledge of German/ Spanish language will be a plus.

We offer:

  • Immediate hire position, incorporation in a first level international company, being part of a dynamic and innovative professional team.
  • Economic conditions will be according to experience and skills provided.
  • Unlimited period contract.

All interested candidates meeting the above requirements should send their CVs with telephone contact details and quoting the reference “Ref. IP Specialist”, either by email to: ecosta@neuraxpharm.com

Apply now


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: 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


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

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