Job Title: Senior Packaging Engineer
Abbott is a global healthcare leader that helps people live more fully at all stages of life.
Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines.
We have been operating in Ireland since 1946 and serve the Irish market with a diverse range of healthcare products including diagnostics, diabetes care, medical devices and nutritional products.
In Ireland, we currently employ about 6,000 people across ten sites located in Dublin, Donegal, Clonmel, Cootehill, Galway, Kilkenny, Longford and Sligo.
Key Responsibilities:
1. Select alternative pack component suppliers to ensure a reliable supply of all packaging materials to third-party manufacturers (TPMs).
2. Collaborate with Packaging Subject Matter Experts (SMEs) to install and validate packaging equipment at TPMs.
3. Identify and implement process improvement projects related to packaging and labeling.
4. Design, develop, and test diverse packaging components (e.g., cartons, inserts, labels, shipper cases) that ensure product protection and handling.
5. Work closely with suppliers to resolve material and quality issues, implementing Corrective and Preventive Actions (CAPA) and Supplier Corrective Action Requests (SCAR).
6. Establish packaging specifications based on product nature, cost constraints, legal requirements, and necessary protection against external variables.
7. Collaborate with cross-functional teams to design package exteriors, considering product identification, sales appeal, and production techniques.
8. Manage documentation and maintain compliance with Good Manufacturing Practices (GMPs).
9. Create and manage change requests and action plans in the document control system as needed.
10. Supervise or guide other engineers and technicians, and participate in cross-functional project teams.
11. Support company initiatives related to Quality Management Systems (QMS), Environmental Management Systems (EMS), and regulatory compliance.
Requirements:
1. Bachelor's degree in a related field or an equivalent combination of education and experience.
2. A minimum of 7 years of progressive technical experience and demonstrated competence, with a strong understanding of regulations and standards affecting division products.
3. Knowledge of FDA, GMP, ASTM standards, and ISO 13485 guidelines.
4. Experience with equipment process validation principles and engineering documentation practices.
5. Strong organizational, problem-solving, and communication skills, with the ability to collaborate effectively within cross-functional teams.
6. Experience in a highly matrixed and geographically diverse business environment.
7. Ability to travel occasionally to support supplier project meetings.
What We Offer:
* Attractive compensation package that includes competitive pay, as well as benefits such as family health insurance, life assurance, fantastic new facility, growing business plus access to many more benefits.