Regulatory Specialist

Regulatory Specialist

Ashington Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Oversee EU, GB, and EMEA authorisations for biocidal products and ensure compliance with chemical regulations.
  • Company: Join a leading manufacturer in the pharmaceutical sector known for innovation and growth.
  • Benefits: Enjoy flexible working options and a supportive corporate culture with great perks.
  • Why this job: Be part of a dynamic team making a real impact in the pharmaceutical industry.
  • Qualifications: A background in regulatory affairs or chemistry is preferred; passion for compliance is key.
  • Other info: This role offers opportunities for professional development and career advancement.

The predicted salary is between 36000 - 60000 £ per year.

The Company

Our client is a specialist in the manufacture for the pharmaceutical sector. Due to growth, they are now looking to recruit a Regulatory Specialist.

The Role

  • Manage and maintain EU, GB and EMEA authorisations of biocidal products;
  • Ensure compliance with other chemical regulations where applicable e.g. CLP;
  • Manage and maintain transitional biocidal registrations.

Regulatory Specialist employer: MTrec Technical

As a leading manufacturer in the pharmaceutical sector, our client offers an exceptional work environment for Regulatory Specialists, characterised by a strong commitment to compliance and innovation. Employees benefit from a collaborative culture that prioritises professional development, with ample opportunities for growth and advancement within the company. Located in a vibrant area, the company also provides unique advantages such as flexible working arrangements and a focus on employee well-being, making it an ideal place for those seeking meaningful and rewarding careers.
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Contact Detail:

MTrec Technical Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Regulatory Specialist

✨Tip Number 1

Familiarise yourself with the latest EU, GB, and EMEA regulations related to biocidal products. Understanding these regulations will not only help you in interviews but also demonstrate your commitment to staying updated in this fast-evolving field.

✨Tip Number 2

Network with professionals in the pharmaceutical and regulatory sectors. Attend industry conferences or webinars where you can meet potential colleagues and learn more about the challenges they face, which can give you an edge during discussions.

✨Tip Number 3

Prepare to discuss specific examples of how you've managed compliance or regulatory submissions in the past. Having concrete experiences ready to share will showcase your expertise and problem-solving skills.

✨Tip Number 4

Research our company culture and values at StudySmarter. Tailoring your conversation to align with what we stand for can make a significant impact during your interview, showing that you're not just a fit for the role, but for our team as well.

We think you need these skills to ace Regulatory Specialist

Regulatory Knowledge
Understanding of Biocidal Products Regulation (BPR)
Familiarity with CLP Regulations
Attention to Detail
Project Management Skills
Strong Communication Skills
Analytical Skills
Problem-Solving Skills
Knowledge of EU and UK Regulatory Frameworks
Experience with Product Submissions
Ability to Interpret Legislation
Time Management Skills
Collaboration Skills
Technical Writing Skills

Some tips for your application 🫡

Understand the Role: Familiarise yourself with the responsibilities of a Regulatory Specialist, particularly in the pharmaceutical sector. Highlight your understanding of EU, GB, and EMEA authorisations and compliance with chemical regulations in your application.

Tailor Your CV: Make sure your CV reflects relevant experience in regulatory affairs, especially with biocidal products. Use specific examples to demonstrate your knowledge of compliance and registration processes.

Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for regulatory work in the pharmaceutical industry. Mention any specific achievements or projects that relate to managing authorisations and compliance.

Proofread Your Application: Before submitting, carefully proofread your application materials. Ensure there are no spelling or grammatical errors, as attention to detail is crucial in regulatory roles.

How to prepare for a job interview at MTrec Technical

✨Know Your Regulations

Familiarise yourself with EU, GB, and EMEA regulations related to biocidal products. Be prepared to discuss how you have managed compliance in previous roles, as this will demonstrate your expertise and understanding of the regulatory landscape.

✨Showcase Your Experience

Prepare specific examples from your past work that highlight your experience with managing authorisations and registrations. Use the STAR method (Situation, Task, Action, Result) to structure your responses effectively.

✨Stay Updated on Industry Changes

Regulatory frameworks can change frequently. Make sure to mention any recent updates or changes in regulations that you are aware of, showing that you are proactive and engaged with the industry.

✨Ask Insightful Questions

Prepare thoughtful questions about the company's approach to regulatory challenges and their future plans. This not only shows your interest in the role but also helps you assess if the company aligns with your career goals.

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