Job Description As a Regulatory Affairs Manager, you will play a crucial role in leading the development and implementation of regulatory strategies for our products in the Latin America region. You will be responsible for preparing and managing filings of regulatory marketing authorization applications, leading assessments and execution of Life Cycle Management changes, and independently researching options for regulatory strategies. Key Responsibilities: - Prepare and manage filings of regulatory marketing authorization (MA) applications in the LATAM territories - Lead assessments and execution of Life Cycle Management changes to provide guidance and support to global teams - Independently researches options for regulatory strategies and presents recommendations at regulatory sub-teams and to leadership Requirements: - Pharmacy degree preferred or BA/BS degree in life sciences - Relevant scientific background with 4-6 years of experience in Regulatory Affairs associated roles in the biotech or pharmaceutical industries with at least two-years of experience in Regulatory Affairs in the LATAM region - The candidate must have hands-on experience with regulatory filings in at least two of the following markets besides Colombia: Mexico, Peru, Ecuador, Argentina, Central America, or Brazil Benefits - Generous vacation time and public holidays observed by the company - Volunteer days - Long-term incentive plans and Employee stock purchase plans - Employee wellbeing benefits - Fitness reimbursement - Tuition sponsoring - Professional development plans