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

Job Offers

R&D QA Internship

R&D QA Internship

July 28, 2017

Position in organization:

 

  • Department: R&D
  • Reporting to: PM Manager
  • Staff in charge: -
  • Location: Esplugues de Llobregat 

Education / experience:

  • Degree in life sciences, preferably in Pharmacy or Chemistry
  • Master’s degree in Chemical or Pharmaceutical Industry
  • Excellent level of scientific English and Spanish, spoken and written.

Previous experience required:

  • Valuable  experience in similar functions in GMP environment
  • Knowledge of GMP.
  • Experience MS Office

Roles and responsibilities:

  • Proposal and management of corrective actions with focus on continuous improvement.
  • Innovation and Risk assessment plans.
  • Managing of all activities of the department: review procedures, guidelines BMR, BPR, CoA etc.
  • Management of deviations, complaints, incidents and investigations
  • Management of Change control and follow up of implementation of actions for internal procedures
  • Management and revision of change controls from CMOs
  • Management of the risk and preventive action system
  • Data storage
  • Review of on-going stabilities of the R&D department
  • Search and propose new partners to work with in the international market.
  • Analyze and propose in the development of new pharmaceutical processes.
  • Research new pharmaceutical routes.

 

Personal Profile:

  • Self-sufficient.
  • Strong analytical skills and problem solving.
  • Highly responsible and capable to work under pressure to meet deadlines.
  • Ability to prioritize multiple tasks
  • Good team player.
  • Strong organizational, planning and time management skills, to achieve project timelines.
  • Detail oriented and good communication and research skills.
  • Motivated, proactive, dynamic, methodical, organized and decisive.
  • Passionated to  grow in QA and R&D department 

Procurement Senior Technician

Procurement Senior Technician

July 24, 2017

Position in organization:

  • Department: Supply Chain 
  • Reporting to: Supply Chain Head
  • Staff in charge: -
  • Location: Barcelona headquarter

 

Education / experience:

  • University degree in Engineering, Economics or Business. 
  • High level of English and Spanish
  • Excellent knowledge of computer sicence, we will value knowledge in Navision and/ or      SAP. For this, the office tools are basic ( advanced excel). 
  • Valuable knowledge in transportation management, foreign trade and experience with suppliers  from China and/ or India. 

 

Previous experience required:

  • Minimum 4 years of experience in similar functions, ideally in the pharmaceutical sector. 

Roles and responsibilities:

  • Ensure the availability  of products to guarantee deliveries to customers and the stock   level.
  • Evaluate and define the security stock of products to buy, ensure the good provision of    the company. 
  • Manage and follow purchase orders through the ERP and is contantly in contact with   suppliers. 
  • Informe internal customer about the order status and update the ERP system with latest and real information. 
  • Prepare transportation and import documentation for products of international suppliers. 
  • Reporting

Personal Profile:

  • Highly responsible, strategic, proactive, dynamic, methodical, decisive and organized individual.
  • Excellent oral and written communication and interpersonal skills.
  • Teamwork and customer orientation, interaction and communication with internal departaments and external suppliers ( mainly China and India). 
  • Strong analytical frame of mind, knows the priorities  of the company and proposes improvements actions. 
  • Capable to work under pressure under your own initiative whilst being a good team player.
  • Strong organizational and time management skills.
  • Detailed oriented 
  • Ability to plan and negotiate, to make materials available on time and to follow retail purchases.

Validation and Transfer Internship

Validation and Transfer Internship

July 24, 2017

Position in organization:

  • Department: R&D 
  • Reporting to: Laboratory Manager
  • Staff in charge: -
  • Location: Esplugues de Ll.

 

Education / experience:

  • Degree in Chemistry
  • Preferably Master’s degree in Analytical Chemistry or Pharmaceutical Industry.
  • Excellent level of scientific and business English, spoken, reading and written.

Roles and responsibilities:

  • Writing Protocols & Reports of analytical validation of new analytical methods for active pharmaceutical ingredient and finished dosage forms.
  • Writing Protocols & Reports of transfers analytical methods between different Sites for active pharmaceutical ingredient and finished dosage forms.
  • Management and review of the documentation provide by CRO’s and CMO’s in reference to the analytical validations & transfers activities.
  • Management of all the material (such standards, samples of finish product, HPLC Columns,etc) needed to complete the activities. (Validations or Transfers)
  • Follow-up of all the tasks that are carrying out.
  • Collect external product methods of analysis current version and edit Galenicum MoA’s.
  • Act as an interlocutor between the transferring laboratory and receiving laboratory.
  • Writing of technical reports and SOP’s (Standards Operating Procedures).
  • Propose improvement flows for the department.
  • Technically guide the staff of whom in charge and provide answers and support to allow them to generate valuable results.
  • Responsibility to replies to deficiency letters.
  • Motivational skills to allow your team to achieve better results with time.
  • Be focused on accomplishing the company goals

Personal Profile:

  • Self-sufficient, critical, disciplined, confident, hard working, creative, motivated, proactive, dynamic, methodical, organized and decisive.
  • Highly responsible and capable to work under pressure to meet deadlines.
  • Excellent organizational, planning and time management skills, to achieve project timelines.
  • Detail oriented professional with good communication skills.
  • Ability to absorb, digest and related detailed scientific, quality and regulatory information.
  • Supportive and able to build effective working relationships throughout the organization.
  • Ability to prioritize multiple tasks and execute projects on time in a fast-paced environment.
  • Ability to use and generate documentation in English.
  • Ability to increase technical knowledge and apply new skills.
  • Availability to travel
  • Strong analytical skills and problem solving.