About the role
Product Safety Associate | Merz Therapeutics (Burlington, ON – Hybrid) Join Merz Therapeutics as a Product Safety Associate supporting pharmacovigilance activities across Canada. This role is responsible for managing adverse event reporting, ensuring compliance with Health Canada and global regulations, and serving as a subject matter expert for the safety database.
You will: Process and assess adverse event and safety reports across marketed and investigational products Ensure timely regulatory submissions to health authorities and partners Analyze safety data, identify trends, and support signal detection Collaborate with global safety teams and support audits, reporting, and compliance activities Contribute to SOP development, training, and continuous improvement initiatives
What we’re looking for: 2–3 years of pharmacovigilance experience within pharma or medical device Strong knowledge of global safety regulations and adverse event reporting Experience with safety databases, medical terminology, and data analysis A detail-oriented, collaborative professional who thrives in a fast-paced environment
At Merz, you’ll be part of a purpose-driven, family-owned organization committed to innovation, inclusion, and putting patients first.
Don’t meet every single requirement? Studies have shown that women and people of color are less likely to apply to jobs unless they meet every single qualification. At Merz Therapeutics we are dedicated to building a diverse, inclusive, and authentic workplace, so if you’re excited about this role but your past experience doesn’t align perfectly with every qualification in the job description, we encourage you to apply anyways. You may be just the right candidate for this or other roles.
Recruitment Note: Merz Therapeutics only sends emails from verified “merz.com” addresses and never asks for sensitive, personal information or money. If you have any doubts about the authenticity of any type of communication from, or on behalf of Merz Therapeutics, please contact Therapeutics.HR@merz.com
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About the role
Product Safety Associate | Merz Therapeutics (Burlington, ON – Hybrid) Join Merz Therapeutics as a Product Safety Associate supporting pharmacovigilance activities across Canada. This role is responsible for managing adverse event reporting, ensuring compliance with Health Canada and global regulations, and serving as a subject matter expert for the safety database.
You will: Process and assess adverse event and safety reports across marketed and investigational products Ensure timely regulatory submissions to health authorities and partners Analyze safety data, identify trends, and support signal detection Collaborate with global safety teams and support audits, reporting, and compliance activities Contribute to SOP development, training, and continuous improvement initiatives
What we’re looking for: 2–3 years of pharmacovigilance experience within pharma or medical device Strong knowledge of global safety regulations and adverse event reporting Experience with safety databases, medical terminology, and data analysis A detail-oriented, collaborative professional who thrives in a fast-paced environment
At Merz, you’ll be part of a purpose-driven, family-owned organization committed to innovation, inclusion, and putting patients first.
Don’t meet every single requirement? Studies have shown that women and people of color are less likely to apply to jobs unless they meet every single qualification. At Merz Therapeutics we are dedicated to building a diverse, inclusive, and authentic workplace, so if you’re excited about this role but your past experience doesn’t align perfectly with every qualification in the job description, we encourage you to apply anyways. You may be just the right candidate for this or other roles.
Recruitment Note: Merz Therapeutics only sends emails from verified “merz.com” addresses and never asks for sensitive, personal information or money. If you have any doubts about the authenticity of any type of communication from, or on behalf of Merz Therapeutics, please contact Therapeutics.HR@merz.com