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Quality Assurance Specialist   

Standort: Schweiz, Tessin, Lugano

Datum: 07/12/2018

Branche: Pharma-Industrie

Funktion: Anderes

Aktivitäten 

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Our client is an international solid, responsible and growing pharmaceutical company based in Ticino.

For this exclusive research, we are looking for a successful candidate to fill the position of:

 

QUALITY ASSURANCE SPECIALIST

 

full time permanent employment in a young working environment and positive culture.

 

Position summary:

This position supports the Corporate Quality Assurance Manager by establishing and maintaining the Corporate Quality System.

 

 

Essential tasks and responsibilities:

  • Analysis and evaluation of monitoring data and key performances indexes in order to insure a continuous improvement of the quality system
  • Complaints management
  • Deviation management
  • Quality investigations and definition of corrective and preventive actions
  • Supplier qualification for finished and semi-finished products, materials, raw materials and their periodic requalification
  • Issuance of Master Batch Records
  • Issuance of validation and qualification protocols and reports
  • Definition of standard operating procedures and GMP-related documentation along with other involved   units/department Managers
  • Definition of training plans for employees along with other involved units/departments Managers
  • Execution of batch record review
  • Involvement in self-inspections
  • Involvement in third parties inspections
  • Issuance of GMP related documents (risk analysis, technical reports, etc.)
  • Change Control

 

Required skills and core competences:

  • Bachelor/Master degree in related technical science (Chemistry, Pharmacy or equivalent)
  • 10 or + years' experience in the Pharmaceutical field, Production or Quality Assurance (experience gained preferably in small-medium Pharmaceuticals)
  • Knowledge of the pharmaceutical industry (expertise in pharmaceutical manufacturing and GMP procedures will be considered an asset)
  • Expertise in sterile injectables
  • Good experience in the use of MS software
  • Fluency in French and English will be considered an asset
  • Strong relational, communication and adaptability skills
  • Ability to work independently and as part of a team
  • 360° commitment to develop expertise on activities requiring high flexibility
  • Able to work independently and as part of a team in order to complete assigned tasks within established deadlines
  • Commitment to continuous improvement

 

Interested candidates should send their CV by email to Cristina Robotti at infoluisoni@luisoni.ch or by post to the address below.

For further information please call the following number: +41 91 911 30 00.
 

We thank all applicants for their interest, but only candidates selected for an interview will be contacted.

MAXIMUM DISCRETION AND PROFESSIONALISM FULLY GUARANTEED.

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Anstellungsart: Dauerhafte Arbeit

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