At a Glance
- Tasks: Assist in the registration and maintenance of veterinary medicinal products worldwide.
- Company: Join Norbrook, a leading veterinary pharmaceutical company with a global impact.
- Benefits: Enjoy attractive salary, 30 days leave, healthcare plan, and employee perks.
- Other info: Great opportunities for career development and a supportive work culture.
- Why this job: Make a difference in animal health while developing your career in a dynamic team.
- Qualifications: Third-level qualification in Sciences and strong organisational skills required.
The predicted salary is between 51750 - 63250 £ per year.
In Norbrook we pride ourselves in being one of the top companies in Northern Ireland and one of the top veterinary pharmaceutical companies globally. We develop & manufacture veterinary medicines, supplying products to 120 countries globally. With a strong portfolio of existing products and significant investment in R&D to launch new products annually, we have opportunities for individuals to join us and develop their career in a global company. Our business strategy is supported by our Values - Customer Value, One Team, Results Driven, Excellence, Innovation, and Quality - and we support our employees to live the behaviours that create our culture. Our on-going success is based on the expertise, knowledge and innovation of our employees. If you are interested in joining our team here at Norbrook and supporting our vision, then apply for this role.
Job Overview
To assist in registration and maintenance of Veterinary Medicinal Products worldwide.
Main Activities/Tasks
- The compilation of regulatory applications for submission to Authorities and third-party Customers worldwide.
- Submission of new product applications and providing support during the assessment and approval processes.
- Maintenance and updating of existing authorisations.
- Responding to external queries from regulatory authorities and customers within strict deadlines.
- Working closely with all departments within Norbrook, providing regulatory support for the operations and control of the facility.
- Analysing scientific data and presenting the information in an organised format.
- Work closely with Customers to ensure all issues are addressed in an efficient and accurate manner.
- Any other duties as deemed necessary by management.
Essential Criteria:
- Educated to a third level qualification or higher in Sciences, preferably a life science.
- Excellent organisational skills along with a proven ability to meet deadlines.
- Meticulous approach and attention to detail with a commercial insight and excellent communication and negotiation skills.
- Ability to work under his/her own initiative and as part of a dynamic regulatory affairs team.
- Ability to analyse scientific data and present this information in an organised format.
- IT skills, particularly in relation to Powerpoint, Adobe and Excel.
Desirable Criteria:
- At least 2 years' experience in the pharmaceutical industry or demonstrate relevant experience.
- Basic knowledge of local, European and Global pharmaceutical regulations of medicinal products.
- Technical file and documentation experience.
- Project Management skills.
Duration: Full Time, Temporary
Location: Newry, Co. Down
Remuneration: Salary Attractive
Benefits: Free Life Assurance, Company Pension Scheme, 30 days annual leave, Wedding Leave, Employee well-being initiatives, Healthcare plan, Company Sick Pay, Employee Assistance Programme, On-site free parking, Canteen Facilities, Employee Perks scheme, Discounted Car Insurance, Annual Employee raffle, employee recognition scheme, career development opportunities and much more.
To Apply
Please forward your CV via the APPLY Now button below.
Regulatory Affairs Associate JBLE1_NI in Newry employer: Norbrook
As an MS&T Site Manager at our Newry location, you will be part of a dynamic and supportive work culture that prioritises employee development and safety. We offer competitive benefits, including opportunities for professional growth and a commitment to maintaining the highest quality standards in manufacturing. Join us to make a meaningful impact while enjoying a collaborative environment that values innovation and teamwork.
StudySmarter Expert Advice🤫
We think this is how you could land Regulatory Affairs Associate JBLE1_NI in Newry
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We think you need these skills to ace Regulatory Affairs Associate JBLE1_NI in Newry
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Norbrook!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Norbrook that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Norbrook!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Norbrook, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Norbrook
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Norbrook that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Norbrook’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
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In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.