Drug Product Operations Engineer: Lean Manufacturing & CI

AbbVie; Sligo; On-site; EUR 55,000 - 75,000; Full time

Job summary

AbbVie in Sligo invites applications for a Drug Product Operations Engineer at the Mannorhamilton Road site. The role focuses on producing drug product material in line with compliance and supporting safe, efficient operations within Drug Product manufacturing.

You will contribute to continuous improvement initiatives, support root cause analyses, and assist in CAPA closures while helping implement and sustain site manufacturing strategies and SOP changes.

Qualifications

• 3-5 years in a similar role in the Pharmaceutical industry.
• 3rd level qualification in an Engineering or related discipline.

Responsibilities

• Play a central role in highlighting and implementing continuous improvement ideas and operational excellence opportunities identified through tracking and monitoring of production performance.
• Assist with the development of lean and continuous improvement skills throughout the manufacturing organization.
• Assist in the pre-campaign planning of Drug Products and APIs, in reviewing lessons learned from previous campaigns with operations personnel and supports post-campaign activities.
• May act as a delegate for the DP and Synthroid Operations Leads for certain activities and tasks based on level of experience and competence.
• Assist and lead Root Cause Analyses and identification of Corrective/Preventative actions as part of investigation processes.
• Assist in following up and closing operations related CAPAs, safety actions and compliance suggestions.
• Implement changes to Operating SOPs as required.
• May represent operations on introductions and execution of NPI projects.
• Assist in the identification, implementation and execution of key Manufacturing and Site Strategies
• Adhere to and supports all EHS & E standards, procedures and policies.

Job description

AbbVie in Sligo invites applications for a Drug Product Operations Engineer at the Mannorhamilton Road site. The role focuses on producing drug product material in line with compliance and supporting safe, efficient operations within Drug Product manufacturing.

You will contribute to continuous improvement initiatives, support root cause analyses, and assist in CAPA closures while helping implement and sustain site manufacturing strategies and SOP changes.