Validation Senior Specialist- Liquir Sterile Production - North Poland

*** Location: North Poland ***

*** Open to relocators ***

*** Fluent Polish Required **

Responsibilities:

  • Conducting qualification and validation of manufacturing equipment, systems, processes for Liquid Sterile Production area by planning and coordinating relevant activities.
  • Preparation and reviewing of procedures and qualification and validation documents
  • Implementation of risk based approach to the validation activities
  • Participation in projects related to production and quality processes
  • Taking part in changes implementation and investigation of deviations
  • Cooperation with external entities related to the implementation of qualification / validation strategy of projects in accordance to current regulations, guidelines and trends in the field of GMP
  • Ability to share knowledge, conducting training and workshops related to validation activities and processes

Qualifications

  • Bachelors/Master’s degree in chemistry, pharma, biotechnology, Life and Science or another closely related discipline;
  • Several years of experience in pharmaceutical environment;
  • Pharmaceutical product knowledge of GMP requirements and pharmaceutical law
  • Knowledge of technology for the production of the pharmacuetical industry
  • Knowledge the issues of commissioning/validation
  • Fluent in English and Polish, both verbal and written.
  • Ability to solve problems and make decisions independently