Genome Editing Regulatory Manager NORLA (Ciudad de México, Ciudad de México, MX)

Genome Editing Regulatory Manager NORLA

About Us

We are a forward-thinking organization committed to delivering innovative and disruptive genome editing products by 2030 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

The Genome Editing Regulatory Manager will play a pivotal role in executing Bayer's crop genome editing regulatory science enablement strategy and shaping regulatory policies related to genome editing technologies within specific countries or regions. This position is crucial to our R&D priorities and requires a strategic thinker who can challenge the status quo and effectively communicate across key stakeholder groups internally and externally. The ideal candidate will possess a deep understanding of plant breeding, genome editing technology, regulatory frameworks, and policy advocacy.

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, global, 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: 877305     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                                 ]]>