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Quality Assurance Manager - Medical Devices

AbbVie

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AbbVie

Quality Assurance Manager - Medical Devices

Onsite Sligo, Ireland Full Time
Posted 12 hours ago
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powertofly approved What AbbVie Has to Offer:

Our work can—and does—have a tangible, lasting impact on millions of people. But it’s not just the results that matter. How we achieve them matters, too. Leading with purpose, we work to build a more sustainable future for generations to come. We do that by putting our expertise, resources and talent to work to make a real difference for patients, communities and our world.

Job Details


Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.


Job Description

AbbVie invites you to join our cutting-edge pharmaceutical facility in Sligo, nestled in a region known for its vibrant community and scenic beauty. Embrace an opportunity to grow your career while contributing to meaningful innovations that enhance global health. 

An exciting role has opened up on our Ballytivnan site in Sligo. We are currently looking for a Quality Manager overseeing the Medical Device Quality team, reporting to the Quality Site Head. You will oversee the whole quality function for the medical device business on site. You'll ensure compliance with quality standards and regulatory requirements,  leading a dedicated team of quality professionals. 

Responsibilities 

  • Quality Assurance & Control: Oversee testing of raw materials, manufacturing quality control, and product validation. 
  •  Team Leadership: Manage and lead a team responsible for compliance and quality oversight. 
  • Regulatory Compliance: Ensure adherence to corporate and regulatory requirements. 
  • Performance Reporting: Report on the performance of the quality management system to senior management. 
  • Issue Resolution: Timely resolution of quality issues and acting as a site representative during regulatory inspections. 
  •  Budget Management: Assist in the development and administration of the quality department's annual budget. 

Qualifications

  • Essential: Bachelor’s degree in science/engineering and 5 years' experience in the healthcare/pharmaceutical industry. 
  • Desired: Master’s degree preferred. 
  • Experience: 6 years in Manufacturing/QA/R&D in relevant industries and 3 years in quality management. 
  • Skills: Familiarity with statistical quality systems, cGMP, and regulatory requirements. Strong leadership, communication, and interpersonal skills are necessary. 
  • Attributes: High attention to detail, commitment to quality, and integrity. 

Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html