Document Management Specialist

2 semanas atrás


Curitiba, Paraná, Brasil Validation & Engineering Group Tempo inteiro

Join our team at Validation & Engineering Group and become a part of a leading services supplier providing solutions for various industries.

Document Control Specialist

As a key member of our team, you will be responsible for designing and revising procedures (SOPs), writing new procedures or performing changes to existing ones as per schedule. You will also develop or review procedures according to established requirements, corporate policies, and regulations.

Key Responsibilities:

  • Design and revise procedures (SOPs)
  • Write new procedures or perform changes to existing ones
  • Develop or review procedures according to established requirements, corporate policies, and regulations

Requirements:

  • Bachelor's degree in science or business administration disciplines
  • 2-5 years of experience in the pharmaceutical industry
  • Experience in Learning and Development processes and management of standard operating procedures in a GMP facility
  • Must be fully bilingual (English / Spanish)

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