Come join our team

Galenicum is a growing company. We believe that our dedicated team is vital to our current and future success. Our HR department is always looking for new candidates to fill positions in a variety of areas. If you are interested in working with us, please send a cover letter along with your CV to:

recruiting@galenicum.com

PRIVACY POLICY

Galenicum Health, S.L. guarantees that we will treat your data with complete confidentiality. For further information, see our Privacy policy.

BASIC INFORMATION CONCERNING DATA PROTECTION

Data controller:

Galenicum Health, S.L.

Data protection officer:

protecciondedatos@galenicum.com

Purpose:

To manage the relationship with candidates for employment with the company.

Legitimation:

Consent.

Recipients:

Your data shall not be disclosed or communicated to third parties, unless required by legal provisions.

Rights of data subjects:

Of access, rectification, deletion, portability, limitation of processing and of opposition to processing, by sending an email to: protecciondedatos@galenicum.com.

Job Offers

Quality Assurance Expert

Quality Assurance Expert

January 11, 2019

Position in organization:

  • Department: Quality Assurance Expert
  • Reporting to: Quality Assurance Manager
  • Staff in charge: -
  • Location: Esplugues de Llobregat

Education / experience:

  • Degree in Pharmacy
  • Master’s degree in Pharmaceutical Industry.
  • Excellent level of English and Spanish, spoken and written.

Previous experience required:

  • GMP knowledge
  • Minimum 3-4 years experience in GMP environment.
  • Minimum 2 years in QC/QA in a Pharmaceutical manufacturing site, preferably with Qualified Person (QP) release responsabilities.
  • Experience MS Office

Roles and responsibilities:

  •  Release activities, by reviewing CoAs, Manufacturing & Packaging Records (BMR, BPR) and management of documentation related.
  • Proposal and management of corrective actions with focus on continuous improvement.
  • Support in the review of Quality Technical Agreements with customers and suppliers.
  • Management of deviations and customer/ suppliers claims. 
  • Management of changes, incidences and nonconformities.
  • Keep updated on GMP regulations and evaluate the impact within our own Quality System and activities.

Personal Profile:

  • Motivated, disciplined, proactive, dynamic, methodical, organized and decisive.
  • Self-sufficient.
  • Strong analytical and problem solving skills.
  • Strong organizational, planning and time management skills, to achieve project timelines.
  • Highly responsible and capable to work under pressure to meet deadlines.
  • Ability to prioritize multiple tasks
  • Detail oriented and good communication and research skills.
  • Capable of working under your own initiative whilst being a good team player.

Derma Customer Care

Derma Customer Care

January 11, 2019

Position in organization:

  • Department: Derma
  • Reporting to: Derma Back-Office
  • Staff in charge: -
  • Location: Esplugues de Llobregat

Education / experience:

  • CFGS or equivalent in Finance and Business administration
  • Desirable SAP experience
  • Excellent computer skills, advanced in Excel.  

 

Previous experience required:

  • Minimum 1 year performing similar functions in customer service department
  • Experience in the field of pharmaceuticals would be an asset

Roles and responsibilities:

  • Opens customer accounts by recording account information
  • Maintains customer records by updating account information.
  • Resolves product or service problems by clarifying the customer's complaint; determining the cause of the problem; selecting and explaining the best solution to solve the problem; expediting correction or adjustment; following up to ensure resolution.
  • Maintains financial accounts by processing customer adjustments
  • Place orders
  • Invoicing
  • Price control
  • Introducing invoices for the customer and supplier in SAP
  • Protects organization's value by keeping information confidential.
  • Help in other requested tasks of the department
  • Verify that transactions comply with financial policies and procedures.

Personal Profile:

  • Highly responsible, disciplined, proactive, dynamic, methodical and decisive individual.
  • Good customer service and quality focus.
  • Solution driven and multitasking
  • Capable to work under pressure under your own initiative whilst being a good team player.
  • Strong organizational and time management skills.
  • Detailed and goal oriented.
  • High level of accuracy.
  • Ability to work with minimal supervision
  • Excellent interpersonal skills.

Pharmacovigilancia Expert

Pharmacovigilancia Expert

January 11, 2019

Position in organization:

  • Department: Clinical Department
  • Reporting to: Clinical Manager and/or Clinical Head
  • Staff in charge: -
  • Location: Office at Esplugues de Llobregat

Education / experience:

  • Pharmacy or life sciences degree
  • Excellent level of business English, spoken and written.
  • Excellent computer skills, specifically Excel, Word, Outlook and Power Point.

Previous experience required:

  • Relevant experience in Pharmacovigilance on EU level
  • Knowledge of EU Pharmacovigilance legislation and preferably experience with data submission to EudraVigilance.
  • The candidate will have a minimum of 2 years of experience in similar functions.

Roles and responsibilities:

  • Role of the qualified person responsible for pharmacovigilance in the EU (QPPV) based on Guideline on good pharmacovigilance practices (GVP).
  • Establishing and maintaining the MAH’s PV system(s): the entire PV/drug safety functioning of the MAH.
  • Ensuring that Quality Control (QC) and Quality Assurance (QA) mechanisms are in place to keep the MAH in compliance.
  • SOPs and Working Documents covering PV are in place, up-to-date, trained on and actually followed.Metrics & KPIs on expedited and aggregate reporting and other key operational functions are tracked.
  • Ensuring that promises made to the Health Authorities in regard to safety are kept.
  • Ensuring that PV training is done in the drug safety/PV department as well as anywhere (everywhere) else in the company (or vendors, third parties etc.) where safety matters may arise
  • Ensuring that written agreements with other companies (including business partners, vendors, other third parties) are in place regarding safety and oversee their work.
  • Ensure that signal detection and trending mechanisms are in place.
  • Ensuring that all suspected adverse drug reactions ADRs received by the MAH are collected and collated and accessible at one or more points in the EU.
  • Ensuring the continuos evaluation of the benefit/risk analyses of all products.
  • Maintaining an overview of the safety profiles and any emerging safety issues on company products.
  • Have access to and ensure that the Pharmacovigilance System Master File (PSMF) is in place, accurate and up to date.
  • Responsible of the training on PhVig matters required for specific areas.

Personal Profile:

  • Highly responsible, proactive, dynamic, methodical, decisive and organized individual.
  • Excellent oral and written communication and interpersonal skills.
  • Strong analytical frame of mind and problem solving.
  • Capable to work under pressure.
  • Strong organizational and time management skills.