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- Tasks: Lead regulatory strategies for innovative products in Professional Hygiene and Crop Protection.
- Company: Join Arxada, a global leader in sustainable solutions and innovation.
- Benefits: Competitive salary, diverse work environment, and opportunities for professional growth.
- Other info: Dynamic team culture with a focus on collaboration and career advancement.
- Why this job: Make a real impact on health and sustainability while working with cutting-edge technologies.
- Qualifications: Master’s degree in natural sciences and 5-10 years in Regulatory Affairs required.
The predicted salary is between 50000 - 65000 £ per year.
Arxada is a global leader in innovative solutions that protect our world. Our groundbreaking technologies, in-depth regulatory know-how, manufacturing and process development help our customers to safeguard nutrition, health and infrastructure efficiently through chemistry and biotechnology that enhance sustainability. We offer a broad portfolio of ingredients and services for multiple end-markets that include Human Health & Nutrition, Home & Personal Care, Professional Hygiene, Paints & Coatings and Wood Protection.
As a Regulatory Affairs Senior Specialist – EMEA, you will play a key role in supporting Arxada’s Professional Hygiene and Crop Protection portfolio within the Microbial Control Solutions business. You will act as both a strategic advisor and a hands‑on regulatory expert, ensuring products meet EMEA regulatory requirements while enabling business growth and innovation.
Working in a matrix environment, you will collaborate closely with colleagues in Regulatory Affairs, R&D, Toxicology, Marketing, and Sales to shape regulatory strategies and deliver successful product registrations across Europe.
Key Responsibilities- Lead regulatory strategy and execution for assigned Professional Hygiene and Crop Protection products across EMEA in compliance with relevant regulations (PPP, BPR, REACH, CLP, and national requirements).
- Act as Regulatory Lead for assigned active substances, owning dossiers and overseeing technical content, submission planning, and procedural compliance with EU authorities (e.g. RMS, co‑RMS, EFSA).
- Coordinate and deliver EMEA product registration activities, including compilation, submission, and lifecycle management of regulatory dossiers (PPP, BPR, national transitional).
- Manage post‑submission activities and interact with regulatory authorities, task forces, and external stakeholders to achieve positive regulatory outcomes.
- Provide clear regulatory analysis, guidance, and recommendations to internal stakeholders and customers to support strategic and commercial decisions.
- Collaborate closely with R&D, Toxicology, and Hazard Communication teams on scientific and technical aspects of regulatory projects.
- Coordinate with consultants and data providers as needed.
- Monitor evolving regulatory requirements and proactively assess and communicate potential impacts on the product portfolio.
- Master’s degree in natural sciences or a related discipline (PhD is an advantage).
- Typically 5–10 years of experience in Regulatory Affairs within the chemical, biocides, or crop protection industry.
- Strong working knowledge of the EU regulatory framework for plant protection products and biocides (PT1–5), with exposure to REACH and CLP.
- Experience with EU Active Substance registration under Regulation (EC) No 1107/2009 is highly desirable.
- Solid scientific understanding of areas such as chemistry, toxicology, ecotoxicology, efficacy, or risk assessment.
- Business‑fluent English with strong written and verbal communication skills.
- Proactive, resilient, and detail‑oriented, with the ability to manage multiple priorities and work effectively under pressure in a matrix organization.
Arxada is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
Regulatory Affairs Senior Specialist in Manchester employer: Arxada
Contact Detail:
Arxada Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Senior Specialist in Manchester
✨Tip Number 1
Network like a pro! Reach out to folks in the industry, especially those already at Arxada. A friendly chat can give you insider info and might just get your foot in the door.
✨Tip Number 2
Prepare for interviews by brushing up on your regulatory knowledge. Be ready to discuss specific regulations like REACH and CLP, and how they apply to the role. Show us you know your stuff!
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, drop a quick thank-you note. It shows your enthusiasm and keeps you fresh in their minds.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re genuinely interested in joining the Arxada team.
We think you need these skills to ace Regulatory Affairs Senior Specialist in Manchester
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Regulatory Affairs Senior Specialist role. Highlight your experience in regulatory strategy and compliance, especially within the chemical or biocides industry. We want to see how your background aligns with our needs!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about regulatory affairs and how your skills can contribute to Arxada's mission. Be sure to mention specific experiences that relate to the job description.
Showcase Your Communication Skills: Since this role requires strong written and verbal communication skills, make sure your application reflects that. Use clear and concise language, and don’t shy away from demonstrating your ability to convey complex regulatory information effectively.
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at Arxada
✨Know Your Regulations
Make sure you brush up on the EU regulatory framework, especially around plant protection products and biocides. Familiarise yourself with key regulations like REACH and CLP, as well as the specifics of the Active Substance registration process. This knowledge will not only help you answer questions confidently but also show your genuine interest in the role.
✨Showcase Your Experience
Prepare to discuss your past experiences in Regulatory Affairs, particularly any hands-on work you've done with product registrations or interactions with regulatory authorities. Use specific examples to illustrate how you've navigated complex regulatory landscapes and contributed to successful outcomes in previous roles.
✨Collaborative Mindset
Since this role involves working closely with various teams, be ready to talk about your collaborative experiences. Highlight instances where you've worked with R&D, Toxicology, or Marketing to shape regulatory strategies. Emphasising your ability to work in a matrix environment will demonstrate that you're a team player who can thrive in their organisational structure.
✨Stay Updated on Trends
Regulatory affairs is always evolving, so show that you're proactive by discussing how you keep up with changes in regulations and industry trends. Mention any resources you follow or networks you’re part of that help you stay informed. This will reflect your commitment to continuous learning and adaptability in a fast-paced environment.