Continuous Improvement Technician
Continuous Improvement Technician
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Job Description
More than a job. Its 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 Coordinator.
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 lets tell you a little more about this role
In your new role you will:
- Coordinate 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 noninventory 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
Qualifications :
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
- 23 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 selfdirected selfmotivated 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!
Additional Information :
AbbVie 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 AbbVies 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 & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
No
Employment Type :
Fulltime
Employment Type
Full-time
