EU Human Safety Technical Quality Lead

Syngenta; Bracknell; Hybrid; GBP 85,000 - 130,000; Full time

Benefits offered by this job

Generous pension scheme

Bonus scheme

Private medical & life insurance

Flexible working

International environment

Training options

Job summary

Syngenta is seeking a Human Safety Technical Quality Manager to lead technical interfaces between internal experts, CROs and regulatory teams across EU submissions. You will shape technical strategy, dossier scope and authority-response plans to ensure scientifically robust, regulatory-ready filings.

In this role you will review CRO deliverables, drive governance and continuous improvement, and mentor teams to translate complex science into pragmatic regulatory decisions.

Qualifications

• Deep Human Safety expertise and strong knowledge of EU plant-protection product regulation.
• Proven experience delivering complex EU dossiers, submissions and authority responses.
• Experience providing technical quality oversight for CRO or outsourced work.
• Ability to turn complex scientific and regulatory issues into pragmatic recommendations.
• Strong planning, judgement and stakeholder-management skills.
• Fluent English.

Responsibilities

• Lead the Human Safety technical interface between internal experts, CROs and project teams.
• Define technical strategy, dossier scope, regulatory positioning and authority-response plans.
• Review and challenge CRO deliverables, ensuring quality from initiation through submission and post-submission support.
• Establish robust handovers, governance, decision records, risk escalation and continuous-improvement actions.
• Strengthen CRO capability through onboarding, training, practical guidance and feedback.
• Advise portfolio teams on feasibility, complexity, resourcing, milestones and delivery dependencies.

Skills

Human Safety expertise

EU regulatory knowledge

Technical leadership

Stakeholder management

Fluent English

Job description

Syngenta is seeking a Human Safety Technical Quality Manager to lead technical interfaces between internal experts, CROs and regulatory teams across EU submissions. You will shape technical strategy, dossier scope and authority-response plans to ensure scientifically robust, regulatory-ready filings.

In this role you will review CRO deliverables, drive governance and continuous improvement, and mentor teams to translate complex science into pragmatic regulatory decisions.