North York, Ontario
Documentation Specialist II (Pharmaceutical Manufacturing/Quality)
4 months contract
Leading pharmaceutical company
Track and review change control documentation.
Assist with the editing of quality documents (SOPs, guidelines, validation master plans, etc.) to ensure compliance with regulator requirements.
Must be able to work quickly with a high degree of accuracy.
Must possess sound interpersonal and information gathering skills, be able to relate well to others at all levels throughout the organization and have the ability to work in a team environment, effectively interacting with others.
Prepare and/or maintain documentation pertaining to programming, systems operation, and user documentation.
Translate business specifications into user documentation.
Plan, write, and maintain systems and user support documentation efforts; including online help screens.
Knowledgeable of commonly used concepts, practices, and procedures within a particular field.
Rely on instructions and pre-established guidelines to perform the functions of the job. .