Quality Specialist (Med Dev/Pharma)

MCS Group; Northern Ireland; On-site; GBP 30,000 - 45,000; Full time

Job summary

MCS Group is recruiting a Quality Specialist for a leading global Medical Device/Pharmaceutical manufacturing company. This exciting role involves working independently and collaboratively to ensure regulatory compliance while addressing quality issues in a rapidly expanding facility. The position is ideal for candidates with a relevant degree and at least two years of experience in quality within the pharmaceutical or medical device sector.

Benefits

25 days' holiday plus 8 bank holidays

Generous employer pension contributions

Private Health Care Cover

Life assurance

Free car parking

Qualifications

• Minimum two years experience in a quality-related role within pharmaceutical/medical device manufacturing.

Responsibilities

• Conduct quality/regulatory activities and ensure compliance with FDA and international regulatory requirements.
• Collaborate with manufacturing and engineering on regulatory compliance issues.
• Develop solutions to problems of moderate to intermediate complexity.

Skills

Regulatory compliance

Problem-solving

Independent working

Education

Degree in Life Science, Engineering, or relevant subject

Job description

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 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