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- Tasks: As a Quality Specialist, you'll tackle quality and regulatory activities in a dynamic manufacturing environment.
- Company: Join a leading global Medical Device/Pharmaceutical company that's expanding rapidly!
- Benefits: Enjoy a lucrative salary, 25 days holiday, private health care, and generous pension contributions.
- Why this job: This role offers a chance to impact healthcare while working with innovative teams and technologies.
- Qualifications: You need a degree in Life Science or Engineering and at least two years in a quality-related role.
- Other info: MCS Group values top-notch service and has a stellar 4.9-star rating on Google!
The predicted salary is between 36000 - 60000 £ per year.
MCS Group is delighted to recruit a Quality Specialist for our successful client, a leading global Medical Device/Pharmaceutical manufacturing company. This is an exciting time to join an expanding manufacturing facility! You will receive: Lucrative salary 25 days' holiday (increasing with length of service) + 8 bank holidays (pro-rata) Bonus Generous employer pension contributions Private Health Care Cover Life assurance Free car parking As the Quality Specialist you will: Work independently to accomplish established objectives, perform varied quality/regulatory activities Work in conjunction with manufacturing, engineering and other functional groups on regulatory compliance issues Develop or participate in the development of solutions to problems of moderate to intermediate complexity Interprets, executes and recommends modifications to operating policies where appropriate Be responsible for fulfilling FDA and international regulatory requirements relevant to each project, such as GMP, IDE, PMA, 510(k) and ISO You will have: A Degree in Life Science, Engineering or a relevant subject Minimum two year's experience in a quality-related role within a pharmaceutical/medical device manufacturing environment To speak in absolute confidence about this opportunity please send an up to date CV via the link provided or contact Kathy Donaghey Senior Specialist Consultant at MCS Group Even if this position is not right for you, we may have others that are. Please visit MCS Group to view a wide selection of our current jobs Not all agencies are the sameMCS Group are passionate about providing a first-class service to all our customers and have an independent review rating of 4.9 stars on Google Skills: Quality Specialist Regulatory Specialist Quality Engineer
Quality Specialist employer: MCS Group
Contact Detail:
MCS Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Specialist
✨Tip Number 1
Familiarize yourself with FDA and international regulatory requirements such as GMP, IDE, PMA, 510(k), and ISO. Understanding these regulations will not only help you in the interview but also demonstrate your commitment to quality standards.
✨Tip Number 2
Network with professionals in the pharmaceutical and medical device industries. Attend relevant conferences or webinars to connect with others in the field, which can provide valuable insights and potentially lead to referrals.
✨Tip Number 3
Prepare to discuss specific examples from your previous experience where you successfully handled quality-related challenges. Highlighting your problem-solving skills will show that you can work independently and contribute effectively to the team.
✨Tip Number 4
Research the company’s recent projects and initiatives in quality assurance. Being knowledgeable about their operations will allow you to ask insightful questions during the interview, showcasing your genuine interest in the role.
We think you need these skills to ace Quality Specialist
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Quality Specialist position. Understand the key responsibilities and required qualifications, as this will help you tailor your application.
Highlight Relevant Experience: In your CV and cover letter, emphasize your experience in quality-related roles within the pharmaceutical or medical device manufacturing environment. Use specific examples to demonstrate your expertise in regulatory compliance and problem-solving.
Showcase Your Education: Mention your degree in Life Science, Engineering, or a relevant subject prominently in your application. If you have any additional certifications related to quality assurance or regulatory affairs, include those as well.
Tailor Your Application: Customize your CV and cover letter to reflect the language and requirements mentioned in the job description. Use keywords such as 'GMP', 'ISO', and 'regulatory compliance' to align your application with what the company is looking for.
How to prepare for a job interview at MCS Group
✨Understand Regulatory Requirements
Make sure you are well-versed in FDA and international regulatory requirements such as GMP, IDE, PMA, 510(k), and ISO. Being able to discuss these topics confidently will show your expertise and readiness for the role.
✨Showcase Problem-Solving Skills
Prepare examples of how you've developed solutions to quality-related problems in previous roles. Highlight your ability to work independently and collaboratively with other teams, as this is crucial for the Quality Specialist position.
✨Demonstrate Your Experience
Be ready to discuss your minimum two years of experience in a quality-related role within the pharmaceutical or medical device manufacturing environment. Specific examples of your past responsibilities and achievements will help illustrate your qualifications.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's quality processes and challenges they face. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.
