Formulation Documentation Coordinator

Enhance your science career with the Formulation Documentation Coordinator role at our Coquitlam location. This hybrid position supports high-quality nutritional product development and involves detailed data and documentation work.

In this 12-month contract role, you will collaborate with cross-functional teams to maintain Master Manufacturing Documents and ensure compliance with Good Manufacturing Practices (GMP). Proficiency in MS Word and Excel is essential for preparing and routing documents, managing change control requests, and supporting data entry across various systems. This is ideal for detail-oriented individuals with a strong scientific background.

Key Responsibilities:

• Build a database for Master Manufacturing Documents

• Prepare and route documents for approval

• Manage Change Control Requests and updates

• Review documentation for accuracy and compliance

• Support document preparation and data entry across systems

Requirements:

• Technical Diploma in Science or Bachelor’s preferred

• Strong MS Word and Excel skills

• Familiarity with Syspro, Asana, or Veeva Vault

• Ability to interpret data into documentation

• Knowledge of GMP is an asset

Leverage your science expertise in documentation and data management within a vibrant formulation team.
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