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Galderma Australia is seeking a Regulatory Affairs & Quality Assurance Associate for their Stockholm office, focusing on the Nordic region. The role involves managing product lifecycle activities in regulatory affairs and quality assurance, requiring a strong background in the pharmaceutical industry, particularly in Nordic markets.
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Job Summary
This is a shared position, with 50% dedicated to Regulatory Affairs (RA) and 50% to Quality Assurance (QA), reporting to the Regulatory Affairs Manager Nordics.
You will play a key role in navigating regulatory landscapes and upholding quality standards, contributing to our mission of delivering safe and effective products to the market.
At Galderma, you will have the opportunity to lead regional operations across multiple markets and gain visibility across both local and global teams.
Matching Summary
Match Score: 75
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Galderma Australia is seeking a Regulatory Affairs & Quality Assurance Associate for their Stockholm office, focusing on the Nordic region. The role involves managing product lifecycle activities in regulatory affairs and quality assurance, requiring a strong background in the pharmaceutical industry, particularly in Nordic markets.
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Skills & Requirements
Must-have
Manage product life cycle across Nordic markets
Support product launches
Maintain national product catalogues
Review and approve labelling and artworks
Establish and maintain quality systems
Manage product complaints and returns
Handle temperature excursions during transportation
Nice-to-have
Contribute to shaping the regulatory environment
Deputize for the Responsible Person
Foster a quality culture
Positive team player
Thrive in dynamic environments
Key Requirements
Pharmacist degree or bachelor's degree in pharmaceutical science or equivalent by experience
3-5 years of experience in Regulatory Affairs
Experience in pharmaceutical Quality Assurance, GDP
Good understanding of the pharmaceutical industry across the Nordic country cluster