Associate Quality Professional

About the role

The Associate Quality Professional will support the Quality Department in delivering compliant, high‑quality diagnostic products and processes. This onsite position at Abbott's Longford facility focuses on ensuring regulatory and company standards are met throughout production and documentation activities.

Key responsibilities

• Complete assigned tasks that support business and quality objectives.
• Maintain accurate, compliant documentation and follow site procedures.
• Support GMP adherence and identify basic process improvements.
• Review and approve documentation such as process orders and inspection records.
• Perform incoming inspection of materials/components where applicable.
• Apply basic risk management principles and support risk documentation (e.g., FMEAs).
• Assist with complaint investigations and ensure proper documentation.
• Support change control activities, including documentation and implementation.
• Participate in design control and validation activities as required.
• Work collaboratively with cross‑functional teams and suppliers.
• Escalate non‑compliance issues appropriately.

Required profile

• Apprenticeship or Bachelor’s Degree in Life Sciences, Engineering, or a related field, or equivalent experience.
• 0‑2 years of relevant experience in a regulated environment.

Required skills

• Basic understanding of regulatory requirements in a healthcare/medical device environment.
• Knowledge of basic risk management techniques, including FMEA.
• Familiarity with Good Manufacturing Practice (GMP) principles.