Continuous Improvement Technician

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

More than a job. It's a chance to make a real difference.

We are now recruiting for a Continuous Improvement Technician to join our to join our New Product Introduction team in Core 1, in AbbVie Westport, Co Mayo. 

In this role you will be responsible and accountable for your own individual area within the team as defined by the Process Improvement Co-ordinator.

We believe in collaboration so in this role, you will partner with management and colleagues across the Core 1 business units including operations personnel across all shifts, QA and the Technical team, articulating the necessary requirements in a clear, concise & persuasive manner.

So let’s tell you a little more about this role…

In your new role, you will:

• Co-ordinate, attend & actively participate in meetings to be aware of all tasks assigned to team members and help/support as required
• Partner with your peers to improve efficiencies, brainstorm and troubleshoot any issues that arise
• Vault: generation, review and approval of assigned documentation. Update SOPs
• GTW: generation and tracking of records
• Change control generation, support and implementation of business unit projects
• Preparation of gamma irradiated non-inventory stock
• Monitoring of Business Unit GTW records daily
• Coordination and preparation of Risk assessments
• Review and control logbooks as required
• Manage requirements to deliver project timelines as required.
• Demonstrate active support and involvement in Continuous Improvement initiatives to enhance the operation of the Biologics Business Unit

So does this role sound exciting? then read on....

To succeed in this role, you will have the following Education and Experience:

• Leaving cert or equivalent qualification required
• 2-3 years GMP experience
• Experience working in an Aseptic/Sterile Manufacturing environment is an advantage
• Excellent computer skills, competency in Microsoft applications including Excel, Word, and PowerPoint is required.
• Excellent planning, organizational, and time & relationship building skills.
• Excellent communication skills
• Ability to use sound judgment to make effective decisions within appropriate timeframes
• Proven to be self-directed, self-motivated and ability to prioritise competing priorities
• Proficiency with Global Track wise & One Vault is preferred
• Understanding of the requirements to work in a regulated GMP industry with knowledge of biologics operations an advantage

So, does this all sound like the right role for you? Apply today!

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

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