At a Glance
- Tasks: Support audits, manage quality complaints, and maintain compliance documentation.
- Company: Join Star People, a leader in UK Regulatory Compliance based in Uxbridge.
- Benefits: Enjoy a structured office environment with opportunities for professional growth.
- Why this job: Be part of a team ensuring product quality and regulatory standards, making a real impact.
- Qualifications: Degree or equivalent experience required; pharma experience is a bonus.
- Other info: Ideal for detail-oriented individuals passionate about quality assurance and compliance.
The predicted salary is between 30000 - 50000 £ per year.
Star People is looking for a reliable and detail-focused Quality Assurance & Regulatory Affairs Associate to join our team. This role plays an important part in supporting both Quality Assurance and Regulatory Affairs activities to ensure we meet all relevant regulations and industry standards.
What you’ll be doing:
- Support the preparation and follow-up for internal and external audits
- Help manage and investigate product quality complaints
- Keep training records, SOPs, and technical agreements up to date
- Support the Responsible Person (RP) with documentation and compliance tasks
- Maintain supplier and customer qualification records
- Stay informed about relevant regulatory guidelines and updates
What we’re looking for:
- A degree or equivalent experience
- Strong organisational skills and attention to detail
- Clear communication and good teamwork
- Experience in pharma or another regulated industry is a plus
- Confident using systems and managing documentation
Quality Assurance and Regulatory Affairs Associate employer: Click To Hired
Contact Detail:
Click To Hired Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance and Regulatory Affairs Associate
✨Tip Number 1
Familiarise yourself with the latest regulatory guidelines and industry standards relevant to Quality Assurance and Regulatory Affairs. This knowledge will not only help you in interviews but also demonstrate your commitment to staying updated in this fast-paced field.
✨Tip Number 2
Network with professionals in the pharmaceutical and regulated industries. Attend industry events or join online forums to connect with others who can provide insights and potentially refer you to job openings, including our positions at StudySmarter.
✨Tip Number 3
Prepare for potential interview questions by practising how you would handle specific scenarios related to quality complaints or audit preparations. Being able to articulate your thought process and problem-solving skills will set you apart from other candidates.
✨Tip Number 4
Showcase your organisational skills by discussing any systems or tools you've used to manage documentation and compliance tasks in previous roles. Highlighting your experience with these processes will align well with what we're looking for at StudySmarter.
We think you need these skills to ace Quality Assurance and Regulatory Affairs Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in Quality Assurance and Regulatory Affairs. Emphasise any specific roles or projects that demonstrate your organisational skills and attention to detail.
Craft a Compelling Cover Letter: Write a cover letter that clearly outlines your passion for the role and how your background aligns with the job requirements. Mention your experience in regulated industries and your ability to manage documentation effectively.
Highlight Relevant Experience: In your application, specifically address the questions about your experience in Regulatory and QA roles. Provide examples of how you've supported audits, managed quality complaints, or maintained compliance records.
Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for this role.
How to prepare for a job interview at Click To Hired
✨Showcase Your Attention to Detail
As a Quality Assurance and Regulatory Affairs Associate, attention to detail is crucial. Be prepared to discuss specific examples from your past experiences where your meticulous nature helped prevent issues or improved processes.
✨Familiarise Yourself with Regulatory Guidelines
Make sure you are up-to-date with the latest regulatory guidelines relevant to the pharmaceutical industry. Being able to discuss recent changes or updates will demonstrate your commitment and knowledge in the field.
✨Prepare for Scenario-Based Questions
Expect questions that assess how you would handle specific situations, such as managing product quality complaints or preparing for audits. Practising these scenarios can help you articulate your thought process and problem-solving skills effectively.
✨Emphasise Teamwork and Communication Skills
This role requires collaboration with various teams. Be ready to share examples of how you've successfully worked in a team environment and communicated effectively with colleagues or stakeholders in previous roles.