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dettaglio posizione
12.11.2019

POSIZIONE CHIUSA

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

MAINTENANCE MANAGER

Responsibilities:
  • 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
 Requirements
  • 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. 


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