This position is on site and will be based in Bogotá, Colombia.
About the Role:
Under direct supervision of the Supervisor of Product Compliance, understand relevant local product-related regulations in cosmetics, foods, supplements and or medical devices in Colombia and coordinate while working with consultants and teammates in Mexico and Peru, and infrequently with other countries, to support product compliance throughout the product lifecycle. Either independently or partnering with other Product Compliance staff, advise relevant stakeholders on the development of product specifications, processes, and product-related materials; gather, compile, and submit (as needed) technical documentation that fulfill pre-market due diligence obligations in order to obtain the necessary regulatory approvals or post market surveillance. Perform other regulatory duties and activities as required to help each country maintain and move forward with stated marketing plans.
What you'll do:
Monitor and interpret relevant regulations through government websites, consultants, publications, trainings, and interactions with officials and trade associations.
Apply current regulations to existing products and recommend changes to formulations, specifications, processes, and product materials.
Manage product registration and notification processes for Colombia and Mexico, working directly with consultants and local authorities.
Finalize technical documents on time and maintain organized regulatory files and archives.
Collaborate with Product Compliance and other teams to ensure compliance across all product-related activities.
Support pre-market due diligence by working directly or indirectly with government agencies.
Respond to technical inquiries from local authorities in coordination with the supervisor.
Recommend improvements to tools and processes that enhance communication and alignment across teams.
Train on and use approved Product Compliance systems and tools.
Communicate clearly in English and work effectively across functions to educate and align stakeholders.
What you'll need:
A degree in Chemical Pharmacy and at least 3-5 years of relevant experience.
Certification and experience as a Technical Director for medical devices.
Familiarity with INVIMA and established working relationships with the agency.
Strong understanding of regulatory environments in the region.
Excellent organizational skills and the ability to manage multiple tasks at once.
Strong written and verbal communication skills in English.
A detail-oriented, proactive, and ethical approach to work.
Ability to work independently and collaboratively in a fast-paced environment.
Basic risk management skills and problem-solving abilities.
Proficiency with standard PC tools (email, word processing, spreadsheets).
Our Benefits & Perks:
You will be part of an engaged, inclusive, global community that values family, giving back, beauty, and sustainability. We offer competitive benefits to eligible employees with comprehensive medical coverage; an incentive bonus program; and access to our top-quality beauty & wellness products. You'll also be empowered to prioritize what's important to you through flexible work arrangements and a vacation policy. Thinking about expanding your family? We have maternity and paternity leave too.
Our Commitment:
We are committed to seeking, developing, and empowering diverse individuals and perspectives. We seek to be a global community where every employee and consumer knows and feels they belong. We are proud to be an equal opportunity employer, and success at Nu Skin is independent of race, age, gender orientation, sexual orientation, religion, or disability.
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