AbbVie
Onsite
Full Time Posted 3 hours ago
Save Job
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

Join AbbVie's Quality Assurance team as an MQA Lead at our Biologics facility in Ballytivnan, Sligo. You will play a key role in ensuring that our marketed and investigational drug products meet global standards, providing quality oversight and guidance for aseptic manufacturing operations in a highly regulated environment.

Responsibilities

  • Ensure all products meet requirements for patients, regulatory authorities, and the company.
  • Provide quality and compliance oversight to operations, supporting aseptic production and intervention observation.
  • Lead investigations into product or manufacturing process non-compliance issues.
  • Guide, train, and support shift team members in decision-making.
  • Review and audit batch records, manufacturing logs, and operational SOPs.
  • Perform line clearance, raw material checks, and maintain product status as required.
  • Lead GEMBAs of manufacturing areas and drive continuous improvement.
  • Act as SME for quality issues during shift operations.
  • Uphold all cGMP, HPRA/FDA, and EHS standards.

Qualifications

  • Third-level degree in science, quality, or engineering.
  • Minimum 3 years' experience in quality/operations in a GMP-regulated environment (biologics preferred).
  • Experience in aseptic processing highly desirable.
  • Excellent written/verbal communication and interpersonal skills.
  • Demonstrated experience in regulatory inspections
  • Proven knowledge of regulatory requirements and strong problem-solving, communication, and interpersonal skills.
  • Previous experience as a trainer
  • Commitment to quality, attention to detail, and Right First Time ethos
  • Previous leadership experience

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

Mission
We're connecting diverse talent to big career moves. Meeting people who boost your career is hard - yet networking is key to growth and economic empowerment. We’re here to support you - within your current workplace or somewhere new. Upskill, join daily virtual events, apply to roles (it’s free!).
Are you hiring? Join our platform for diversifiying your team
Post a job
MQA Lead
Save Job