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Senior Document Controller

$ 6,000 - $ 9,000 / month

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Senior Consultant – Document Controller

Responsibilities:

  • Ensure documentation compliance with Data Integrity and ALCOA++ principles.
  • Review and complete qualification protocols for pharmaceutical systems (e.g., CTUs, BSCs, Autoclaves).
  • Mentor and oversee junior consultants in documentation and protocol reviews.
  • Apply knowledge of qualification tests for pharmaceutical systems.
  • Report any issues encountered during execution to the Project Manager.

Requirements:

  • Extensive experience in CQV activities within the pharmaceutical/biotech industry.
  • Strong understanding of Data Integrity and ALCOA++ principles.
  • Proven experience in quality assurance and documentation review.
  • Expertise in qualifying CTUs and storage systems (e.g., freezers, cold rooms).
  • Technical degree in Engineering, Chemistry, Biotechnology, or related fields.
  • At least 8 years of experience in the pharmaceutical sector.
  • Fluent in English (C1 level or above).
  • Strong teamwork, communication, and leadership skills.
  • Full on-site availability.

(EA Registration: 20C0196)
(R22108971)

Senior Consultant – Document Controller

Responsibilities:

  • Ensure documentation compliance with Data Integrity and ALCOA++ principles.
  • Review and complete qualification protocols for pharmaceutical systems (e.g., CTUs, BSCs, Autoclaves).
  • Mentor and oversee junior consultants in documentation and protocol reviews.
  • Apply knowledge of qualification tests for pharmaceutical systems.
  • Report any issues encountered during execution to the Project Manager.

Requirements:

  • Extensive experience in CQV activities within the pharmaceutical/biotech industry.
  • Strong understanding of Data Integrity and ALCOA++ principles.
  • Proven experience in quality assurance and documentation review.
  • Expertise in qualifying CTUs and storage systems (e.g., freezers, cold rooms).
  • Technical degree in Engineering, Chemistry, Biotechnology, or related fields.
  • At least 8 years of experience in the pharmaceutical sector.
  • Fluent in English (C1 level or above).
  • Strong teamwork, communication, and leadership skills.
  • Full on-site availability.

(EA Registration: 20C0196)
(R22108971)