home | archivio posizioni | network 
chi siamo
dove siamo
posizioni aperte
Ricerca nell'archivio delle posizioni

dettaglio posizione


Our customer is an important company, operating in the pharmaceutical field in Ticino area. We are beginning the recruitment process for the following profile:


  • support the design development, procurement, factory acceptance testing, installation, commissioning and qualification of the Facility Utilities systems
  • maintaining the utilities and process equipment once the site is fully GMP.  
  • responsible during the project for the commissioning and qualification of the Industrial Services and Clean Services 
  • maintain and operate the utilities and process equipment 
  • ensure that commissioning and qualification activities are performed according to GEP, GMP, GAMP respecting current technical, environmental and safety norms
  • contribute to project success by managing milestones and respecting defined budget
  • define and ensure that User Requirements are followed in collaboration with key users and participate to procurement process and suppliers selection
  • as maintenance expert, participate to the design development of the biotech process equipment
  • ensure that appropriate project documentation & training is provided at projectís hand over and prepare the spare part inventory at projectís reception
  • develop and implement the overall preventive, corrective and predictive maintenance programs
  • develop maintenance procedures and work instructions for the Facility systems
  • develop the maintenance training program and provide training to operative staff
  • develop, implement and then administrate the Siteís maintenance planning system for tracking maintenance work orders, spare parts and maintenance history of plant equipment
  • ensure that the systems are operated and maintained by strictly following the technical norms, safety rules and GMP regulations
  • keep records of equipment failures and provide needed information and data to the equipment owners
  • manage all technical related issues that will affect the day to day operation of the new plant
  • ensure a complete traceability of the maintenance and qualification activities following the Company's compliance procedures and cGMP rules
  • contribute to the development of Siteís standards
  • ensure that the systems are ready for inspection at all time and provide support during regulatory inspections
  • ensure close collaboration with operation users and QA and contribute to continuous improvement of the systems and processes overall
  • ensure that all procedures and technical documents are updated according to the Site quality documentation systems
  • in collaboration with QA and Manufacturing department, contribute to the harmonization of the commissioning and qualification activities that are planned within the project
  • stay up to date on latest industry standards
  • ensure safe working conditions
  • contribute positively to a strong culture of business integrity and ethics
  • act within compliance and legal requirements as well as within company guidelines
  • technical and/or Engineering educational background preferably in Mechanics, Electricity, Automation
  • 7+ years of experience in the pharma/biotech manufacturing environment 
  • good knowledge of Biotech/Pharma Utilities systems and equipment
  • understanding of electrical standards and local requirements, certifications
  • strong project management skills with good knowledge of Design, Construction activities
  • strong interpersonal and communications skills; written and oral
  • fluent in English and Italian. Knowledge of German is a plus
  • Broad and experiential knowledge of Pharmaceutical Quality, Manufacturing and GMP practices
If your experience fits with the listed requirements please send your application to Mr. Alberto Largader (largader@lwphr.ch) who is in charge for the selection.

No reply will be given to the non-compliant applications. 

posizioni aperte