Chemgineering is an international Consulting and Engineering service provider located in Switzerland, Germany, Austria, Spain, Mexico, Poland and Serbia. We specialize in creating efficient workflows and realizing high tech projects in various areas of the life science industries like Pharma, Biotech, Fine Chemicals, Medical Devices, Food and Consumer Care and Cosmetics.

tick ES - Senior Consultant Qualification & Validation (m/f/d)



Location: Barcelona

 

Your tasks

Tasks: technical

  • Planning, execution and coordination of engineering project-specific qualification and validation activities according to current GMP regulations
  • Preparation of high-level qualification & validation documents
  • Execution of GxP risk analyses
  • Preparation of test plans and reports (DQ, IQ, OQ, PQ as well as for CSV-Aspects in these kind of projects)
  • Qualification coordination (interface between technical engineers, customers and suppliers)
  • Execution of qualifications (DQ, IQ, OQ, PQ as well as for CSV-Aspects in these kind of projects)
  • Support in the technical training of the Qualification & Validation department

Tasks: business development

  • Build a department for Q&V services, autonomous but integrated with the rest of the company’s service portfolio
  • Assume responsibility for the commercial results of the department
  • Sell Q&V services to customers based on a network of customer contacts 
  • Preparation of proposals and cost calculation for customers
  • Integration of operations with other company departments and with engineering project managers when required
  • Grow the technical delivery team in line with turnover growth
  • Grow the knowledge for the Q&V area of expertise within the team
  • Coordinate the introduction of technical and standards, in alignment with Q&V teams in other parts of the Group

 

Requirements

To be successful in this position you need

  • Completed studies in a technical or scientific field (e.g. studies in pharmacy, chemistry, process engineering, food technology or comparable / training as industrial foreman FR pharmacy, FR chemistry or comparable / preferably also only with several years of professional experience as a pharmaceutical technician, chemical technician or shift supervisor in the field of production or packaging of pharmaceuticals/medical products)
  • Professional experience (>= 5 years) in the pharmaceutical/medical device industry with expert knowledge in the area of qualification/validation
  • Familiar and confident handling of current GMP regulations
  • Willingness to travel regularly in Spain and also in Central Europe (also for longer periods, up to 5 days/week)
  • Very good / Native Spanish language, English in high level written and spoken, German would be an advantage
  • Ability to work in a team as well as independently and in a structured manner 
  • Strong assertiveness is a plus

If you are looking for an opportunity to participate in major international projects and develop a successful career in an international company, we are looking forward to your application!  

 

 

Any more questions?
Please ask:

Ms Tanja Hermann
career@chemgineering.com

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