Regulatory Strategy Lead - Health & Wellness (CDMX)

2238 Sanofi-Aventis de Mexico S.A de CV; Ciudad de México; On-site; MXN 900,000 - 1,100,000; Full time

Job summary

Opella is seeking a Regulatory Lead to shape regulatory strategy for its products, ensuring timely health authorizations and alignment with local and global requirements. You will collaborate with internal teams and stakeholders to manage lifecycle events and ensure compliant advertising strategies.

The role emphasizes leadership, regulatory risk assessment, and engagement with health authorities to support brand initiatives and product development.

Qualifications

• Bachelor’s degree in Chemical-Biological Sciences (with degree awarded) or related fields.
• Master’s degree desirable.
• 3–5 years in Science Affairs/pharmaceutical experience (Medical, Regulatory, R&D or similar), including leadership roles.
• Regulatory Affairs, Quality, Manufacturing, Pharmacovigilance, Development, Clinical Research, or related health fields.

Responsibilities

• Design the regulatory strategy for the products under your responsibility, coordinating with the Center of Expertise and submitting classification consultations, registrations, and renewals to obtain health authorizations.
• Review and define strategy for global/local assessments for new products or projects.
• Lifecycle management of the products (renewals, modifications, IPP updates, etc.).
• Provide regulatory input in Brand & Innovation events and ensure advertising materials comply with regulations.

Skills

Regulatory Affairs

Pharmaceutical experience

Leadership

Education

Bachelor’s degree in Chemical-Biological Sciences

Master’s degree desirable

Job description

Opella is seeking a Regulatory Lead to shape regulatory strategy for its products, ensuring timely health authorizations and alignment with local and global requirements. You will collaborate with internal teams and stakeholders to manage lifecycle events and ensure compliant advertising strategies.

The role emphasizes leadership, regulatory risk assessment, and engagement with health authorities to support brand initiatives and product development.