Jobs / Ireland / Abbvie INC

Abbvie INC

Process Improvement Technician

Westport, MO, IE Posted today

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Skills this job asks for

Inventory managementCommunicationExcel

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Sponsorship verdict

No sponsorship evidence yet

No government record and no wording either way. Not a refusal: ask the recruiter.

  • No government sponsor record hereNo government sponsor record covers this employer in this country.
  • The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
  • Can’t check pay against the visa rulesNo salary stated. Ireland Critical Skills Employment Permit needs at least €40,904 a year (General Employment Permit: €36,605).
  • Confirmed live todayWhen a source last listed this job as open.
Details and sources
Can’t check pay against the visa rules
No salary stated. Ireland Critical Skills Employment Permit needs at least €40,904 a year (General Employment Permit: €36,605). Source: https://enterprise.gov.ie/en/what-we-do/workplace-and-skills/employment-permits/permit-types/critical-skills-employment-permit/, rules effective 2026-03-01.

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Before you apply

Sponsorship unknown

No register record and no sponsorship wording in the posting. Worth asking the employer before investing significant time.

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About the role

The Process Improvement Technician is responsible for supporting production related duties such as review of logbooks, updating of DtoA and DtoA vault documents on Vault, generation and inputting of Maximo Production Schedule and supporting gamma irradiation of non-inventory stock. This role is responsible for department change controls and continuous improvements within Core1 – generation of Change controls and actions on GTW, scheduling meetings and supporting implementation as required. • 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 to BU SOPs • GTW: generation and tracking of records and Monitoring of Business Unit GTW records daily • Generation and inputting of monthly production schedule on Maximo • Change control generation, support, and implementation of BU projects • Preparation of gamma irradiated non-inventory stock • 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 • 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 • Excellent computer skills, competency in Microsoft applications including Excel, Word, and PowerPoint is required. • Excellent planning, organizational, and time & relationship building skills. • Proficiency with Global Track wise, Maximo & One Vault is preferred • Understanding of the requirements to work in a regulated GMP industry with knowledge of biologics operations an advantage 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 US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

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