Abbott Posted October 16, 2026

FPRT Lab Technician

Kilkenny, State Not Indicated, Ireland FULL_TIME
Notify me about similar jobs

Abbott is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Abbott in Ireland

Abbott has maintained a strong presence in Ireland since 1946 and celebrates its 80th anniversary in the country in 2026. The company supports the Irish healthcare sector with a broad portfolio spanning diagnostics, diabetes care, medical devices and nutritional products. Today, Abbott employs more than 6,500 people across ten sites located in Dublin, Donegal, Clonmel, Cootehill, Galway, Kilkenny, Longford and Sligo.

 

About Abbott

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.

Abbott Diabetes Care Kilkenny

Abbott Diabetes Care has opened a new site, in Kilkenny, that is  at the forefront of Diabetes care with the latest technology, to manufacture Freestyle blood glucose test strips and Freestyle Sensors for use in diabetes management. Among Abbott Diabetes Care leading brands are the Freestyle Precision, Freestyle Lite and Freestyle Libre systems.

Main purpose of the role

To perform all set up, preparation and testing of sensors via Portal test system so that testing is performed on time, in full meeting all quality and compliance requirements, and in a cost-effective manner to meet the needs of the business & the customer. The role includes performing laboratory duties such as preparing buffers and performing validity testing using specified equipment. The person within the role will perform verifications of their colleagues’ actions and undertake batch record reviews and approvals, to support product batch release. Perform inspections associated with laboratory investigations and / or technical / quality system investigations and generate associated reports. he person will assist in the scheduling and control of testing to ensure all scheduled testing is performed correctly in a timely manner. The role is individually accountable for the quality and efficiency of their own actions whilst performing sensors testing, and via verifications also responsible for the actions of their colleagues.

To maintain awareness of new/changed products and processes within the area, and to proactively support projects and drive improvements in terms of quality, cost and efficiency.

The person undertaking the role will ensure their actions are compliant with Health and Safety regulations and standards by adhering the sites Health and Safety systems and procedures. Being accountable for the health and safety of themselves and others by highlighting where EHS improvements can be made.

Main responsibilities

Operate laboratory equipment following Standard Operating Procedures (SOPs).

Perform troubleshooting and problem solving online following guidance in SOPs.

Prepare solutions according to SOP’s, accurately weighing raw materials and performing calculations,

Perform the associated Inventory Management transactions (i.e. generation of batch numbers and material usage transactions).

Perform basic engineering functions (i.e. set-up checks and routine maintenance of laboratory equipment) and consistently maintain a high standard of housekeeping.

Maintain good timekeeping for all tasks and to wear correct working attire and PPE.

Perform cleaning of glassware and utensils and maintain the laboratory in a clean and fit condition for use

Ensure sufficient stocks of all laboratory consumables available ready for use.

Assist in the scheduling and control of testing and making sure all scheduled testing is performed correctly in a timely manner to ensure output targets and schedules are met.

Perform Out of Specification investigations as per SOP, where applicable.

Undertake the verification of data and documentation reviews as required.

To adhere to training policies and procedures; being aware of their, and other Technician training status to ensure it is up to date prior to performing tasks and making sure they remain in compliance within the sites training system.

Perform training of fellow Technicians.

To know, understand and adhere to Health and Safety risk assessments applicable to the area.

Pro-actively prevent/reduce the occurrences of non-conformances within the sensor testing area, and support non-conformance investigations, in addition to any associated corrective and / or preventative actions.

Support audit readiness for internal and external quality system audits.

Through role model behaviour, demonstrate full cross functional team support for the department and ancillary functions.

Communicating details of laboratory activities with line managers and representing workgroup if and when required Ensure that any support functions, such as Engineering Support, or Unit Quality Assurance and Technical Support are notified in a timely manner.

To always adhere to company policies and procedures and input data accurately into production records.

To perform any other reasonable request.  Note: This job description describes the principal and main elements of the job. It is a guide to the nature and main duties of the job as they currently exist but is not intended as a wholly comprehensive or permanent representation.

Qualifications & Experience

A Level 7 or Level 8 qualification in a relevant science or engineering discipline, or equivalent.

Experience of working in a laboratory or product test environment and use of a variety of analytical/testing instruments, to provide a general knowledge of laboratory science is preferred.

Basic computer skills are required to operate Laboratory based computer applications and equipment.

Exposure to working in a regulated environment where strict compliance and documentation discipline is preferred.

Meticulous attention to detail – maintaining accuracy and consistency in high-volume, time-sensitive testing

Accountability - for both personal actions and verification of colleagues’ work

Compliance mindset, strict adherence to Quality, GLP & Health & Safety standards

Proactive risk prevention & Problem solving - spotting potential problems & resolving efficiently

Effective communicator, able to escalate issues promptly and represent the workgroup when required

Time Management & Prioritisation-ability to manage schedules and ensure timely completion of testing.

Health & Safety Awareness - strong commitment to EHS compliance and proactive identification of safety improvements.

What we Offer

Attractive compensation package that includes competitive pay, as well as benefits such as

Family health insurance,

Excellent pension scheme

Life assurance

Career Development

Fantastic new facility

Growing business plus access to many more benefits.

 

Important Information

Please note that any offer of employment is conditional upon the successful completion of a pre-employment medical examination, including drug and alcohol screening, conducted by a Company-designated medical practitioner.

Connect with us at www.abbott.com or https://www.ie.abbott/, on LinkedIn at www.linkedin.com/company/abbott-/, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.

Abbott is an equal opportunities employer.

Job details

Seniority
Not listed
Function
Quality
Therapeutic area
Not listed
Location
Kilkenny, State Not Indicated, Ireland
Employment type
FULL_TIME

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 1369 comparable Quality roles across 143 biopharma companies.

1369Comparable roles tracked
1241Currently active
143Companies hiring similar roles
52Countries represented

Salary context

230 of 1369 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · QA - Stat Sort Specialist · Lilly $18/hr – $35/hr (≈ $37,482–$72,592/yr)
Highest disclosed · Vice President, Quality Assurance - GMP · Exelixis Inc $315,500/yr – $366,500/yr
Peer group range $55,037 – $341,000 (median $129,052)

Where these roles are based

Top locations among the 1369 comparable roles

United States554
Ireland81
China62
France58
Germany51
India50

+ 46 more countries

Seniority mix

625 of 1369 peers have a known seniority level

Manager183
Senior166
Intern/Fellow/Postdoc73
Associate68
Associate Director35
Director35
Principal30
Senior Director28
Executive/VP7

Therapeutic area mix

1 of 1369 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
McDermott Laboratories Limited Northern Cross, Ireland Manager
Same function Same country
40%similar
Mylan Teoranta Inverin, Ireland Manager
Same function Same country
40%similar
Mylan Teoranta Inverin, Ireland Director
Same function Same country
40%similar
Mylan Teoranta Inverin, Ireland
Same function Same country
40%similar
Mylan Teoranta Inverin, Ireland
Same function Same country
40%similar
Mylan Teoranta Inverin, Ireland Senior
Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
Senior Manager, Global Device Quality
McDermott Laboratories Limited · Northern Cross, Ireland · Manager
Function Therapeutic area Seniority Country
40%
Quality Assurance Documentation Controller
Mylan Teoranta · Inverin, Ireland · Seniority not listed
Function Therapeutic area Seniority Country
40%
Sr QA Validation Specialist
Regeneron Ireland · Limerick, Ireland · Senior
Function Therapeutic area Seniority Country
40%
Senior QA Validation Specialist
Regeneron Ireland · Limerick, Ireland · Senior
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.