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Process Validation Specialist

Job Description

Antal International is a multinational headhunting company with more than 130 offices in 35 countries.

Life Science is a team specialized in talented engineering profiles in production, SCM, R&D, construction, quality, design and technical S&M.

 

THE COMPANY

Multinational Medical Devices Manufacturer Company

 

THE ROLE

 

 

Process Validation Specialist

 

Main responsibilities:

 

  • Preparation of validation plans, protocols, reports and procedures of critical process and equipment (PQ/OQ);
  • Managing validation projects;
  • Execution in cooperation with involved departments of equipment and process validation;
  • Filling in validation protocols;
  • Collecting information from involved departments to prepare validation documents;
  • Review and integration in company system protocols and reports from suppliers.
  • Preparation of plans, protocols, reports and procedures of computer system validation;
  • Supporting the coordinator in preparation and updating Validation Master Plan;
  • Performing statistical data analysis.
  • Qualifications, experience, know-how and skills critical for success

 

PERSONAL ATTRIBUTES

 

  • Scientific degree (Biotechnology, Pharmacy, CTF, Chemistry, Engineering);
  • 4 years in process validation regulated industry
  • Technical knowledge:    Biomedical standards, ISO standards,   FDA standards
  • B2 level of English

 

LOCATION: SOUTH OF MILAN

 

Please send your CV to - RIF: LRimmauro@antal.com Process Validation Specialist – Sud di Milano

 
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Contact

Luca Rimmauro
+39 02 80 60 601
Italy