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Regulatory Affairs Specialist

1 semana atrás


Loures, Lisboa, Portugal TN Portugal Tempo inteiro
Job Description
  • We are looking for a Quality Assurance Specialist to join our team in TN Portugal.
  • The ideal candidate will have a university degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences or a similar scientific field and at least 3 years of experience in a QA GMP environment within the Pharmaceutical Industry.

The Quality Assurance Specialist will be responsible for ensuring cGMP compliance in all activities and systems related to projects and products execution.

Key responsibilities include implementing policies, procedures and methods to evaluate and continuously improve the quality of products and operations throughout the product lifecycle.