Regulatory affairs specialist

Cannara Biotech (Québec) inc

Farnham, QC

• Under the responsibility of the VP Compliance and General Manager, the
Regulatory Affairs specialist will be responsible for developing, facilitating and
execute comprehensive regulatory strategies through all phases of
product development and life cycle, accelerate and ensure
successful product registrations for product launches and management
changes for marketed products.
• Manage licensing and communications with Health Canada;
• Provide regulatory requirements expertise to other departments during
product development or proposed product changes
approved (including R&D, manufacturing, quality assurance, quality control and
marketing);
• Research and analyze regulatory information and determine acceptability of
product data, procedures and other documentation submitted in support of
Product registration;
• Prepare, review, analyze and consolidate all information required for
initial or post-approval regulatory submissions to competent authorities, y
including Health Canada;
•... More Detail

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