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- Tasks: As a Quality Specialist, you'll tackle quality and regulatory activities in a dynamic environment.
- Company: Join a leading global Medical Device/Pharmaceutical manufacturer with a strong reputation.
- Benefits: Enjoy a lucrative salary, 25 days holiday, private health care, and generous pension contributions.
- Why this job: Be part of an expanding facility, making a real impact on healthcare and compliance.
- Qualifications: A degree in Life Science or Engineering and two years' experience in quality roles are required.
- Other info: Contact Kathy Donaghey for more details or explore other opportunities at MCS Group.
The predicted salary is between 28800 - 42000 £ 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
- Interpret, execute and recommend 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 years' 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 028 96935521.
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 www.mcsgroup.jobs.
Quality Specialist (Med Dev/Pharma) employer: MCS Group
Contact Detail:
MCS Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Specialist (Med Dev/Pharma)
✨Tip Number 1
Familiarise yourself with the latest FDA and international regulatory requirements, especially those related to GMP, IDE, PMA, and ISO. This knowledge will not only help you in interviews but also demonstrate your commitment to the role.
✨Tip Number 2
Network with professionals in the medical device and pharmaceutical industries. Attend relevant conferences or webinars to connect with potential colleagues and learn about industry trends that could give you an edge.
✨Tip Number 3
Prepare to discuss specific examples from your previous experience where you successfully handled quality-related challenges. Highlight your problem-solving skills and how you collaborated with other departments to achieve compliance.
✨Tip Number 4
Research the company’s values and recent developments in their manufacturing processes. Tailoring your conversation to align with their goals can show that you are genuinely interested in contributing to their success.
We think you need these skills to ace Quality Specialist (Med Dev/Pharma)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in quality assurance within the pharmaceutical or medical device sectors. Emphasise any specific projects or responsibilities that align with the job description.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for quality assurance and your understanding of regulatory compliance. Mention your degree and how your two years of experience make you a suitable candidate for this role.
Highlight Relevant Skills: In your application, clearly outline skills that are pertinent to the role, such as knowledge of FDA regulations, GMP, and ISO standards. Use specific examples to demonstrate your expertise in these areas.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a Quality Specialist.
How to prepare for a job interview at MCS Group
✨Understand Regulatory Standards
Familiarise yourself with FDA and international regulatory requirements such as GMP, IDE, PMA, 510(k), and ISO. Being able to discuss these standards confidently will demonstrate your expertise and readiness for the role.
✨Showcase Problem-Solving Skills
Prepare examples of how you've developed solutions to quality-related issues in previous roles. Highlighting your ability to tackle moderate to intermediate complexity problems will impress interviewers.
✨Collaborative Mindset
Emphasise your experience working with cross-functional teams, such as manufacturing and engineering. Discussing how you’ve collaborated on regulatory compliance issues will show that you can work well in a team-oriented environment.
✨Highlight Relevant Experience
Be ready to discuss your degree in Life Science or Engineering and how your two years of experience in a quality-related role have prepared you for this position. Tailoring your responses to reflect the job description will make you a strong candidate.
