A

Abbott

Makes heart devices, glucose sensors and lab tests

Quality Professional

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timeLongford, IrelandNo salary listed

About the Job

Requirements

  • An apprenticeship or relevant third-level qualification in Life Science, Engineering, or a closely related discipline is required, or a relevant combination of education or experience.
  • At least three years of work experience in Quality or a related field is required; less experience may be appropriate with an advanced degree.
  • Demonstrates understanding of how their function supports the business.
  • Demonstrates technical and business competencies that drive results and continuous improvement.

Responsibilities

  • Conduct quality-related activities to deliver consistent, high-quality documents, services, products, and processes that add value to the business.
  • Contribute to defining and timely achieving overall project goals, provide compliant solutions to problems of moderate scope and complexity, and interact constructively with employees, managers, and cross-functional peers.
  • May lead a limited-scope project and contribute to broader projects; provide guidance to other Professionals and Technicians. Scope is typically limited to one specific QA function.
  • Maintain awareness of standards that regulate the industry and ensure compliance with site-level policies and procedures by promptly reporting non-compliance issues to management within the Division and Corporation as appropriate.
  • Maintain vigilance to ensure adherence to the Quality Policy and Quality System procedures by promptly reporting non-compliance issues to management.
  • Apply basic Risk Management principles to work.
  • Receive general direction, exercise discretion to own work details, and recommend possible solutions.
  • Ensure compliant documentation and carry out tasks related to the area of responsibility with management oversight; make decisions that may have short- and long-term impact.
  • Complete process order and documentation reviews and approvals, and complete incoming inspection of raw materials and components according to approved receiving documentation.
  • Participate in developing or modifying Risk Management files.
  • Investigate complex complaints with management oversight and provide compliant solutions to complex problems.
  • Identify areas for process improvement and provide supporting information for changes, including reasons and justifications; process changes according to the appropriate procedure.
  • Coordinate quality decisions between quality and engineering groups, participate in developing or modifying validation packages, design plans, and Risk Management deliverables such as FMEAs, and interface with suppliers to deliver products that meet quality requirements.

About the Company

Abbott

Makes heart devices, glucose sensors and lab tests

Abbott makes medical devices, diagnostic tests, nutrition products and branded generic drugs for hospitals, laboratories, pharmacies and patients. Its best-known product is the FreeStyle Libre, a coin-sized sensor worn on the upper arm that tracks blood sugar around the clock without routine finger pricks. Its other lines run from heart valves, pacemakers and brain stimulators to lab analyzers, rapid tests and mail-in colon cancer screening kits, and Abbott earns money by selling these products to health systems, labs, retailers and consumers. The company was founded in 1888 by Chicago physician Wallace Abbott and is based in Abbott Park, Illinois.

Company size
10,001+
Company stage
IPO
Headquarters
Abbott Park, IL
Founded
1888

Recently Posted Jobs

Explore more opportunities at Abbott

See more jobs