Regulatory Affairs Specialist (Santiago)

Regulatory Affairs Specialist (Santiago)

03 ago
|
Sandoz
|
Santiago

03 ago

Sandoz

Santiago

- Achieve the best product registration with commercially attractive labelling in accordance with registration plan -Maintain and secure product license in terms of CMC/CDS/safety update according to local regulations/law/guidelines, company strategy and global compliance -Ensure compliance with NP4, KRPIA code of conduct, relevant regulations and laws for related CPO activities (DRAGON update, RMP, packing materials, promotional materials/activities, PMS/drug safety reporting etc.) -Foster and maintain good relations with internal and external stakeholders -Reporting of technical complaints / adverse events / special case scenarios related to Sandoz products within 24 hours of receipt -Distribution of marketing samples (where applicable)

Major Accountabilities

- Achieve the best product registration with commercially attractive labelling in accordance with registration plan -Maintain and secure product license in terms of CMC/CDS/safety update according to local regulations/law/guidelines, company strategy and global compliance -Ensure compliance with NP4, KRPIA code of conduct, relevant regulations and laws for related CPO activities (DRAGON update, RMP, packing materials,



promotional materials/activities, PMS/drug safety reporting etc.) -Foster and maintain good relations with internal and external stakeholders -Reporting of technical complaints / adverse events / special case scenarios related to Sandoz products within 24 hours of receipt -Distribution of marketing samples (where applicable)

Key Performance Indicators

- Project & stakeholder feedback -Product license update in terms of CMC in agreed timeline -Adherence to Sandoz policy and guidelines

Minimum Requirements

Work Experience

- Minimum of 3 years of Regulatory Affairs experience within pharmaceutical companies in Chile.
- Strong knowledge of regulatory processes and requirements with the Institute of Public Health (ISP).
- Experience preparing regulatory submissions for new product registrations and lifecycle maintenance of pharmaceutical products.
- Adaptable mindset, adaptable to change, and proactive approach to work.
- Provide your feedback on BizChat

Languages

- English.

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📌 Regulatory Affairs Specialist (Santiago)
🏢 Sandoz
📍 Santiago

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