Be at the heart of actionFly remote-controlled drones into enemy territory to gather vital information.

Apply Now

Advisor, FSQR Regulatory Affairs EMEA Cocoa & chocolate

Cargill
London
3 days ago
Create job alert

Cargill’s size and scale allows us to make a positive impact in the world. Our purpose is to nourish the world in a safe, responsible and sustainable way.

We are a family company providing food, ingredients, agricultural solutions and industrial products that are vital for living. We connect farmers with markets so they can prosper. We connect customers with ingredients so they can make meals people love. And we connect families with daily essentials — from eggs to edible oils, salt to skincare, feed to alternative fuel. Our 160,000 colleagues, operating in 70 countries, make essential products that touch billions of lives each day. Join us and reach your higher purpose at Cargill.

Job Purpose and Impact

The Regulatory Product Group Lead will identify, set and drive regulatory activities and strategic direction for a cocoa and chocolate product group and throughout the EMEA region internally and externally. In this role, you will work closely with research and development, food safety quality and regulatory operations and relevant functions. You will partner with a broad set of key stakeholders to define and enable compliance systems and processes to enable commercial teams to establish and achieve business objectives and growth strategies.

Key Accountabilities

  • Be the main regulatory and scientific affairs contact across functions for Cocoa and Chocolate product group including product lines, key customers and commercial leaders.
  • Provide strategy and guidance and coordinate the regulatory affairs initiatives within a product group in the region to define the regulatory compliance for existing products and products destined for export.
  • Provide thought leadership in regulatory and scientific affairs area in the region including midterm and long term emerging issues.
  • Partner with food safety quality and regulatory, and research and development colleagues to assess and implement programs and processes that enable regulatory compliance and innovation and priorities.
  • Monitor, understand, anticipate and interpret regulatory changes and share and train related functions to improve partnering and effectiveness.
  • Develop and coordinate regulatory positions, requirements and processes and work with commercial teams, functional units, key customers, trade associations and external regulatory agencies.
  • Develop strong coordination and connections globally within our product groups and regionally across product groups to leverage synergies, ensure continuous development and enable capacity building for executing regulatory compliance and innovation.
  • Provide expert thought leadership in your field and work with limited direction, using additional research and interpretation to identify issues or problems. You may provide direction to supporting team members and be a strategic contributor.
  • Other duties as assigned

Qualifications

Minimum Qualifications

  • Bachelor’s degree in science or food law; or equivalent experience
  • Advanced knowledge of food laws and regulations relevant to cocoa and chocolate product group
  • Active participation in key Trade Association (s) in the region
  • Minimum of 8 years of related work experience
  • Experience in Cocoa & Chocolate is a must

Preferred Qualifications

  • Master's degree in science or law
  • Min 10 - 15 years of professional regulatory experience
  • Strong relationship with government agencies in the region
  • Active participation in key Trade Association(s) in the region
  • Advanced knowledge of food laws & regulations in EU & Cocoa Chocolate Subject matter expert and ensuring compliance with food laws and regulations

Our Offer

We provide a fast paced stimulating international environment, which will stretch your abilities and channel your talents. We also offer competitive salary and benefits combined with outstanding career development opportunities in one of the largest and most solid private companies in the world.

Interested? Then make sure to send us your CV and cover letter in English today:

Follow us on LinkedIn: https://www.linkedin.com/company/cargill

Cargill is committed to being an inclusive employer. Click here to find out more https://careers.cargill.com/diversity/

Related Jobs

View all jobs

Advisor, Fsqr Regulatory Affairs Emea Cocoa & Chocolate

Health & Safety Advisor

Clinical Consultant

Global Quality Manager

Technical Manager

Recruitment Consultant

Subscribe to Future Tech Insights for the latest jobs & insights, direct to your inbox.

By subscribing, you agree to our privacy policy and terms of service.

Industry Insights

Discover insightful articles, industry insights, expert tips, and curated resources.

Neurodiversity in Medical Technology Careers: Turning Different Thinking into a Superpower

Medical technology sits at the intersection of health, engineering & innovation. From imaging & diagnostics to digital health apps, wearables & surgical robotics, medtech is about solving complex real-world problems that directly affect patients’ lives. To do that well, the sector needs people who think differently. If you live with ADHD, autism or dyslexia, you may have been told your brain is “too distracted”, “too literal” or “too disorganised” for a regulated, safety-critical industry. In reality, many traits that made school or previous jobs difficult can be huge strengths in medical technology – from pattern-spotting in clinical data to meticulous attention to detail in device testing. This guide is for neurodivergent job seekers exploring medical technology careers in the UK. We’ll cover: What neurodiversity means in a medtech context How ADHD, autism & dyslexia strengths map to common medtech roles Practical workplace adjustments you can ask for under UK law How to talk about your neurodivergence in applications & interviews By the end, you’ll have a clearer sense of where you might thrive in medical technology – & how to turn “different thinking” into a genuine superpower.

Medical Technology Hiring Trends 2026: What to Watch Out For (For Job Seekers & Recruiters)

As we move into 2026, the medical technology (MedTech) jobs market in the UK is changing fast. Hospitals and health systems are under pressure to do more with less. Diagnostics and devices are becoming smarter, more connected and more regulated. AI, robotics and remote monitoring are no longer “future tech” – they’re being built into mainstream care pathways. At the same time, budgets are tight, funding cycles are uneven and some healthtech start-ups are consolidating or being acquired. That means fewer vague “innovation” roles and more focus on medical technology jobs that directly support regulatory approval, patient safety, NHS adoption and commercial growth. Whether you are a MedTech job seeker planning your next move, or a recruiter building teams for medical device, diagnostics or digital health companies, this guide breaks down the key medical technology hiring trends for 2026.

Medical Technology Recruitment Trends 2025 (UK): What Job Seekers Need To Know About Today’s Hiring Process

Summary: UK medical technology hiring has shifted from title‑led CV screens to capability‑driven assessments that emphasise regulatory‑aware product delivery (QMS, ISO 13485), software lifecycle & risk (IEC 62304/14971), usability (IEC 62366), clinical & regulatory strategy (MDR/UKCA), device cyber security & privacy, and measurable patient/clinical and commercial impact. This guide explains what’s changed, what to expect in interviews & how to prepare—especially for SaMD engineers, AI/ML in medical devices, product & quality engineers, regulatory/clinical affairs specialists, validation/verification, manufacturing/operations, and digital health roles. Who this is for: Software/firmware engineers in medtech, SaMD/AI engineers, systems & verification engineers, quality & regulatory affairs (QARA), clinical evaluation/PMCF specialists, human factors engineers, medical device cyber security & privacy, test/validation, manufacturing & operations, field/service engineers, and medtech product managers in the UK.