Job DescriptionMore 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 requiredPartner with your peers to improve efficiencies, brainstorm and troubleshoot any issues that ariseVault: generation, review and approval of assigned documentation.
Update SOPsGTW: generation and tracking of recordsChange control generation, support and implementation of business unit projectsPreparation of gamma irradiated non-inventory stockMonitoring of Business Unit GTW records dailyCoordination and preparation of Risk assessmentsReview and control logbooks as requiredManage requirements to deliver project timelines as required.Demonstrate active support and involvement in Continuous Improvement initiatives to enhance the operation of the Biologics Business UnitQualificationsSo 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 required2-3 years GMP experienceExperience working in an Aseptic/Sterile Manufacturing environment is an advantageExcellent computer skills, competency in Microsoft applications including Excel, Word, and PowerPoint is required.Excellent planning, organizational, and time & relationship building skills.Excellent communication skillsAbility to use sound judgment to make effective decisions within appropriate timeframesProven to be self-directed, self-motivated and ability to prioritise competing prioritiesProficiency with Global Track wise & One Vault is preferredUnderstanding of the requirements to work in a regulated GMP industry with knowledge of biologics operations an advantageSo, does this all sound like the right role for you?
Apply today Please note: Closing date for applications is the 11th April 2025Additional InformationAbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie's policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.US & Puerto Rico only - to learn more, visit US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn