Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Support the Pharma division with regulatory compliance and documentation in the pharmaceutical industry.
- Company: Join Brenntag, a global leader in chemical distribution with a collaborative culture.
- Benefits: Enjoy competitive salary, bonus scheme, 25 days holiday, and career progression opportunities.
- Why this job: Make a real impact in the pharmaceutical sector while working in a hybrid environment.
- Qualifications: Degree or experience in life sciences and knowledge of pharmaceutical regulations required.
- Other info: Be part of a diverse team that values innovation and equal opportunities.
The predicted salary is between 30000 - 50000 £ per year.
Location: Any Brenntag office within UK / Ireland (Hybrid - 2 days working from home)
Contract Type: Full-time, Permanent
About Brenntag UK & Ireland:
Brenntag UK & Ireland is part of the global Brenntag Group, the world’s leading distributor of chemicals and ingredients. Headquartered in Leeds, we operate across 21 strategic sites in the UK and Ireland, including three sea-fed facilities, and serve over 20,000 customer accounts with the support of a dedicated fleet of 100+ vehicles. As a market leader, we offer a comprehensive portfolio of industrial and specialty chemicals, along with value-added services such as blending, filling, technical support, and regulatory expertise. Our work spans a wide range of industries including life sciences, environmental, and material sciences. Globally, Brenntag connects over 170,000 customers and suppliers through a network of more than 600 sites in 70 countries.
Key Responsibilities:
- Support the regional Pharma division Sales Team on regulatory, legal, compliance, quality, and product safety topics related to raw material supply into the pharmaceutical industry.
- Complete technical and regulatory documentation and respond to customer information requests (e.g., questionnaires, supply chain agreements, QAA’s & TA’s).
- Source information internally and from suppliers to satisfy customer requests.
- Report and document customer requests via KPIs.
- Manage Process Change Control Notifications.
- Collaborate with commercial and value-added services teams on regulatory topics for customer projects.
- Work with QHSE & supply chain teams to ensure regulatory compliance and support implementation of new standards (IPEC GMP/GDP, EXCiPACT, GDP).
- Participate in EMEA Pharma Regulatory team projects.
- Create and manage product regulatory information in a standardised format.
- Provide training on regulatory topics to commercial and supply chain teams.
- Undertake any other tasks within capability to support the commercial success of the Pharma business unit.
Candidate Requirements:
Essential:
- Degree or significant experience in life sciences.
- Knowledge of pharmaceutical industry requirements and regulations on APIs, excipients, biopharma, and traditional pharma raw materials.
- Understanding of European National Competent Authority requirements for distribution of APIs, excipients, and raw materials.
- Fluent in English (spoken and written).
- Strong collaboration, communication, and interpersonal skills with the ability to work proactively across all levels and functions.
Desirable:
- Experience working with regulatory documentation.
- Knowledge of GxP requirements in Pharma and/or Biopharma.
Employee Benefits:
- Competitive salary and annual bonus scheme.
- 25 days holiday plus bank holidays.
- Pension plan and life assurance.
- Access to learning and development opportunities.
- Employee assistance programme and wellbeing initiatives.
- Career progression within a global organisation.
Equal Opportunities Statement:
Brenntag provides equal employment opportunities to qualified applicants and employees of all backgrounds and identities to create a workplace where difference is valued because it forms a resilient and more innovative organization. We do not discriminate on the basis of age, disability, gender identity, sexual orientation, ethnicity, race, religion or belief, parental and family status, or any other protected characteristic. We welcome applications from women, men and non-binary candidates of all ethnicities and socio-economic backgrounds.
Ready to take the next step? Apply today and join our team driving excellence in pharmaceutical regulatory affairs!
Regulatory Affairs Specialist - Pharmaceuticals in Leeds employer: Brenntag
Contact Detail:
Brenntag Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Specialist - Pharmaceuticals in Leeds
✨Tip Number 1
Network like a pro! Reach out to professionals in the regulatory affairs field on LinkedIn or at industry events. A friendly chat can open doors that a CV just can't.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of pharmaceutical regulations and compliance. We recommend having specific examples ready to showcase your experience and skills.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, drop a quick thank-you email to express your appreciation and reiterate your interest in the role.
✨Tip Number 4
Apply through our website for the best chance at landing that Regulatory Affairs Specialist role. It shows you're serious about joining Brenntag and helps us keep track of your application!
We think you need these skills to ace Regulatory Affairs Specialist - Pharmaceuticals in Leeds
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Regulatory Affairs Specialist role. Highlight your experience in life sciences and any relevant knowledge of pharmaceutical regulations. We want to see how your background fits with what we do at Brenntag!
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 you can contribute to our team. Be sure to mention specific experiences that relate to the job description.
Showcase Your Communication Skills: Since this role involves collaboration across teams, make sure to highlight your strong communication skills in your application. We love candidates who can articulate their thoughts clearly and work well with others!
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re serious about joining our team at Brenntag!
How to prepare for a job interview at Brenntag
✨Know Your Regulations
Make sure you brush up on the key regulations and requirements in the pharmaceutical industry, especially around APIs and excipients. Being able to discuss these confidently will show that you’re not just familiar with the basics but also understand the nuances of the role.
✨Prepare for Technical Questions
Expect questions about regulatory documentation and compliance standards like IPEC GMP/GDP and EXCiPACT. Prepare specific examples from your past experience where you successfully navigated these areas, as this will demonstrate your hands-on knowledge.
✨Showcase Your Collaboration Skills
Since the role involves working closely with various teams, be ready to share examples of how you've effectively collaborated in the past. Highlight any cross-functional projects you've been part of and how you contributed to their success.
✨Ask Insightful Questions
At the end of the interview, don’t forget to ask questions that show your interest in the company and the role. Inquire about the team dynamics, ongoing projects in the Pharma division, or how they ensure compliance with evolving regulations. This shows you’re genuinely interested and engaged.