REGULATORY AFFAIRS ADVISOR

Description

Job Summary: A leading pharmaceutical company is seeking a Regulatory Affairs Advisor to promote products, build strong relationships, and manage regulatory files and procedures with health authorities. Key Highlights: 1. World leadership in pain treatment 2. Product promotion and relationship building with healthcare professionals 3. Career development within a solid company in the sector **BACHER ZOPPI is seeking a REGULATORY AFFAIRS ADVISOR in Álvaro Obregón, Mexico City** ----------------------------------------------------------------------------------------- A leading global pharmaceutical company specializing in pain treatment and related diseases is seeking a highly motivated **REGULATORY AFFAIRS ADVISOR** to promote products and build strong relationships with healthcare professionals. **REQUIREMENTS:** * Completed undergraduate degree (graduated or intern) in Pharmacy (QFB), Pharmaceutical Engineering, or Pharmacy Minimum 1–2 years of experience in regulatory affairs or quality assurance Experience in any quality area (quality assurance, quality management) or pharmaceutical regulatory affairs is acceptable. Strong communication skills and ability to work independently Results-oriented, skilled in negotiation, and proactive attitude **COMPENSATION AND BENEFITS:** * Competitive monthly salary Statutory benefits Year-end bonus (aguinaldo) Vacation time IMSS registration Vacation premium Work tools **Work Location:** Torre Aleph, Av. Insurgentes Sur 2475\-16th, Tizapán San Ángel, San Ángel, Álvaro Obregón, 01090 Ciudad de México, CDMX **RESPONSIBILITIES:** * Responsible for collecting, reviewing, analyzing, and selecting scientific information, and preparing regulatory dossiers for new product registrations or product modifications, ensuring compliance Support dossier preparation (e.g., drafting letters for which templates already exist—such as biological product releases, payment refund requests, submission of controlled substance test results), and assist in preparing biological product releases, advertising permits, and contract manufacturing authorizations Review, prepare, and submit import permits, advertising permits, contract manufacturing notifications, finished product releases, etc., to the corresponding health authorities. If you meet the profile and seek career growth within a solid company in the sector, we invite you to apply by submitting your updated **CV**. **Desired Education Level:** Higher education \- graduated **Desired Experience Level:** Mid-level **Departmental Function:** Medicine / Health **Industry:** Pharmaceuticals *This vacancy originates from the Talenteca.com job board:* *https://www.talenteca.com/anuncio?j\_id\=6a0775d136000036008e722d\&source\=indeed*