CAPA Engineer

Abbott Ireland

In Ireland, Abbott employs around 6,000 people across ten sites. We currently have six manufacturing facilities located in Clonmel, Cootehill, Donegal, Longford and Sligo and a third-party manufacturing management operation in Sligo. Abbott also has commercial, support operations and shared services in Dublin and Galway. We have been making a difference in the lives of Irish people since 1946.

Diabetes Care Kilkenny

Our new manufacturing facility in Kilkenny, reflects the growing demand for Abbott's global Diabetes Care products. The facility will be a centre for world-class engineering, quality, medical device manufacturing, and other science-based professionals to produce life-changing technologies that enable people with diabetes to live the best and fullest lives they can. At Abbott in Kilkenny, you can shape your career as you help shape the future of healthcare.

This is how you can make a difference at Abbott:

As a CAPA Engineer you will facilitate and execute the CAPA process. You will also support continuous improvement and effective maintenance of the QMS. Ensure the use of appropriate risk management tools to prioritise activities.

Key Responsibilities

• Participate in the completion of CAPA projects, ensuring compliance, and quality of records.

• Collaborate with cross-functional teams using various methodologies (e.g. Six Sigma root cause analysis/problem solving skills).

• Independently investigate, gathers data, and perform preliminary analysis.

• Process requests, ensuring owners are assigned, and timely responses and approvals are provided in alignment with quality goals.

• Identify trends potential issues, improvement initiatives.

• Ensure on-time completion of Quality Assurance engineering deliverables.

• Support team in the delivery and oversight of CAPA training program.

• Identify projects to enhance and promote effectiveness, and efficiency of the quality system and product quality.

• Support Operations to make Quality / Compliance decisions on product during processing, manufacturing, testing, monitoring and packaging.

• Provide support and subject matter expertise during audits and inspections.

Qualification and Experience

• Minimum Level 7 NFQ qualification or equivalent in a relevant discipline.

• Min of 4 years  experience in Engineering/Manufacturing/Scientific environment.

• Previous CAPA and/or quality assurance/engineering experience.

• Ability to demonstrated use of quality tools/methodologies.

• Prior medical device experience preferred.

• Knowledge of FDA Quality System Regulations (21 CFR Part 820), GMP, and ISO 13485: 2016.

• Good communication and interpersonal skills.

• Previous project management and leadership skills, including the ability to lead multi-departmental project teams and resolve quality-related issues in a timely and effective manner.

• Advanced computer skills, including statistical/data analysis and report writing Skills

What we Offer

Attractive compensation package that includes competitive pay, as well as benefits such as

• Family health insurance,

• Excellent pension scheme

• Life assurance

• Career Development

• Fantastic new facility

• Growing business plus access to many more benefits.

Connect with us at www.abbott.com or https://www.ie.abbott/, on LinkedIn at www.linkedin.com/company/abbott-/, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.

Abbott is an equal opportunities employer.