Analista de Assuntos Regulatórios Pleno

Laboratorios Biopas; São Paulo; Presencial; BRL 20.000 - 80.000; Tempo integral

Resumo da oferta

A leading company in pharmaceutical manufacturing is looking for a Regulatory Affairs Analyst. This role involves ensuring compliance with local regulations and requires experience in the pharmaceutical industry. Candidates with a solid regulatory background and proficiency in English are encouraged to apply.

Qualificações

• Minimum of 3 years of experience in the Pharmaceutical Industry.
• Solid knowledge of local regulatory requirements for medicines.
• Deep technical knowledge in regulatory affairs.

Responsabilidades

• Ensure products meet all necessary regulations.
• Support regulatory submissions and compliance activities.

Conhecimentos

Familiarity with PATE elaboration

Knowledge of local regulatory requirements

Proficiency in English language

Basic knowledge of Spanish

Descrição da oferta de emprego

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We are seeking a Regulatory Affairs Analyst to join our team. This is an opportunity for someone with experience in the pharmaceutical industry and regulatory affairs. In this role, the candidate will play a key part in ensuring that our products meet all necessary regulations.

Requirements:

• Availability to work 100% in person from Monday to Friday
• Minimum of 3 years of experience in the Pharmaceutical Industry, in similar positions
• Solid knowledge of local regulatory requirements – applicable for medicines or synthetic medicines
• Deep technical knowledge
• Familiarity with PATE elaboration
• PICs Guidances and OCH Guidelines knowledge
• Proficiency in the English language
• Basic knowledge of Spanish

If you are passionate about regulatory affairs and want to make a significant impact in the pharmaceutical industry, we would love to hear from you!

Additional Information

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Job function: Other
• Industries: Pharmaceutical Manufacturing, Retail Pharmacies, Wholesale Drugs and Sundries