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Head environmental regulatory affairs

Rotkreuz
Festanstellung
Roche
Inserat online seit: 21 Januar
Beschreibung

Overview

Join to apply for the Head Environmental Regulatory Affairs role at Roche. This role focuses on leading environmental regulatory affairs within the Diagnostics division, ensuring compliance and strategic advocacy.


Responsibilities

* Lead and coordinate Diagnostics’ representation in external associations (e.g., MedTech Europe, AdvaMed, APACMed) and at European Commission meetings to set the global strategy for advocacy on environmental and sustainability topics.
* Represent Diagnostics at the Roche Group Level in cross‑functional committees, including the Emerging Legislation Committee, to ensure divisional interests are integrated into corporate strategies.
* Track and monitor global environmental regulatory changes and support the implementation strategy for requirements that impact Diagnostics' right to operate.
* Accountable for the alignment and implementation of mQMS GSP01 requirements and provide expert support and guidance directly to sites and affiliates.
* As a people leader for the environmental regulatory affairs team, provide strategic direction, actionable guidance, and opportunities for employee development, training, and education.
* Establish and lead appropriate Diagnostics affiliate networks while partnering closely with the Dia Regulatory Policy Team and Government Affairs to provide expert advice and coaching.
* Manage budget responsibilities and serve as an active member of the Diagnostics Product Sustainability and Compliance leadership team.


Qualifications

* Hold at least a Master of Science degree in chemistry, biology, or a related field; additional training in environmental and chemical regulations is a bonus.
* 10+ years of experience working on product‑related environmental regulations.
* Expert communicator capable of influencing complex internal and external stakeholders in a matrix environment and translating complex topics into an easily understandable format.
* Strong, demonstrated experience working within industry associations and direct interaction with authorities, preferably within the diagnostics and medical device sector.
* Strategic visionary with the ability to build strong relationships, work independently, and influence without authority through analytical and innovative thinking.
* Dedicated to radical simplification, trust, and a leadership style that experiments and learns for the benefit of patients and the business.


Benefits & Compensation

Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Rotkreuz. Compensation details for additional locations will be provided later in the hiring process.


Job Details

* Seniority level: Mid‑Senior level
* Employment type: Full‑time
* Job function: Quality Assurance and Consulting
* Industries: Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing

Ready for the next step? We look forward to hearing from you. Apply now to discover this exciting opportunity!

Roche is an Equal Opportunity Employer.

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