**Genome Editing Regulatory Manager NORLA**
**About Us**:
We are a forward-thinking organization committed to delivering innovative and disruptive genome editing products by **** and beyond.
Our team is dedicated to pushing the boundaries of research and development in the field of genome editing, and we are seeking a dynamic individual to join us as a Genome Editing Regulatory Manager.
**Role Overview**:
**Key Responsibilities**:
- Develop and implement regulatory policy advocacy strategies to support the advancement of genome editing technologies within the designated country or region.
- Monitor and analyze regional regulatory trends and policy developments related to genome editing in the broader context of seed and biotechnology regulations.
- Engage with regional regulatory bodies, industry groups, and other stakeholders to advocate for favorable regulatory environments.
- Collaborate with cross-functional teams to ensure alignment on regulatory strategies and priorities.
- Provide expert guidance on regulatory status determination and compliance requirements.
- Draft, prepare, and manage regulatory submissions to enable the product pipeline, ensuring timely and accurate filings with regional regulatory authorities.
- Lead and manage projects related to regulatory policy advocacy and regulatory affairs within the region.
- Communicate complex regulatory and policy concepts clearly and effectively to diverse audiences.
- Build strong relationships with regional teams and stakeholders to effectively execute Bayer's Regulatory Genome Editing Enablement strategy.




**Qualifications**:
- PhD preferred; Master's degree required in a relevant field (e.g., genomics, plant breeding, biotechnology, regulatory affairs).
- Proven experience in genome editing technology, plant breeding, and regulatory policy.
- Prior experience in an AgTech R&D; environment considered a plus.
- Strong project management skills with the ability to manage multiple priorities in a fast-paced environment.
- High proficiency in English (both written and verbal) is required; additional languages are a plus.
- Ability to work effectively in a collaborative, general, multicultural environment.
- A forward-thinking mindset with the ability to challenge conventional approaches.
- Willingness to speak up and advocate for innovative solutions.
**Why Join Us**:
- Be part of a pioneering team dedicated to transforming the future of genome editing in agriculture.
- Work in a dynamic and fast-paced environment that values innovation and creativity.
- Collaborate with talented professionals across the world.
- Contribute to the development of groundbreaking products that have the potential to change lives and advance sustainable agriculture.
**Período de aplicación**:
- 22 Julio al 05 Agosto
**Código de referencia**:
- ******
**División**:
- Crop Science
**Ubicación**:
- Mexico : Ciudad de México : Ciudad de México
**Área funcional**:
- Registro Farmacéutico
**Grado de posición**:
- VS 1.3
**Tipo de empleo**:
- Permanente
**Tiempo de trabajo**:
- Indefinido - Full Time

📌 Genome Editing Regulatory Manager Norla (Xico)
🏢 Bayer
📍 Xico