Manufacturing Shift Manager - Biologics

Do your best work at AbbVie—as part of a brilliant, curious team

We are currently sourcing an experienced Manufacturing Shift Manager to join our Biologics Manufacturing team in AbbVie Westport on a permanent basis. In this role you will lead and facilitate the safe operations of the 24/7 Biologics manufacturing team in a bio-pharmaceutical processing facility in line with all safety, regulatory and operational requirements.

This is a shift based role, you will be required to work 12-hour shifts between days and nights on a monthly rotation. 

As part of your new and exciting role you will assure the long-term effectiveness of the team: deliver high levels of customer service, ensure quality of product and services, comply with all regulatory requirements, achieve desired financial performance including cost reductions, and build a culture of high performance for the team

Does this interest to you? then read on....

Here's a snapshot of your key responsibilities for this role:

• Act as key point of technical contact for aseptic fill finish activities. 
• Supervision and execution of compounding, filling, lyophilization, equipment preparation, formulation, buffer preparation and support processing activities in the biologics fill finish facility to meet clearly stated operating objectives
• You will lead, coach & mentor your manufacturing team, across a 12-hour rotating shift, to maximize the effectiveness through clear and effective communication of task details and goals to their team members, to allow the biologics technicians to work effectively
• As part of this diverse and inclusive team, you will conduct on the floor promotion of a culture of contamination control and compliance with aseptic best practice.
• Communicate the departmental goals, to provide cost effective quality compliant products in a safe, effective manner
• We believe in collaboration so in this role, you will liaise with program management, supply chain, technical operations quality and engineering groups to ensure effective planning, scheduling and execution of commercial and NPI clinical manufacturing
• Resolve operations/project issues by working with team members, project customers, and others as appropriate.
• Responsible for driving operations excellences and Key operations targets including OEE where applicable
• Provides direct interface as a subject matter expert with QA department to interaction with HPRA, FDA and applicable health authority and internal audits