AbbVie Posted August 31, 2026

QC Lab Supervisor - Days

Sligo, SO Full-time
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AbbVie 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

Company Description

About AbbVie

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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at  www.abbvie.com . Follow @abbvie on  LinkedIn,   Facebook ,  Instagram ,  X  and  YouTube.

Job Description

AbbVie is seeking an experienced QC Supervisor to lead a team of laboratory analysts within our Quality Control function in Sligo. This role is responsible for ensuring that raw materials, in-process samples, finished products, stability studies, and contract testing activities are completed to the highest quality standards, on schedule, and in compliance with GMP and regulatory requirements.

As QC Supervisor, you will provide leadership and coaching to a team of 2-12 analysts, driving laboratory performance, data integrity, compliance, and continuous improvement initiatives. You will oversee day-to-day laboratory operations, support investigations, ensure equipment and systems compliance, and collaborate cross-functionally with Manufacturing, Quality Assurance, and Supply Chain teams.

Key Responsibilities

Lead, coach, and develop a team of QC analysts to drive performance and quality excellence.

Ensure compliance with GMP, Data Integrity, HPRA/FDA, and internal quality requirements.

Oversee laboratory testing activities and ensure adherence to testing schedules.

Drive continuous improvement, Right First Time (RFT), and operational excellence initiatives.

Lead analytical investigations, OOS/OOT events, root cause analysis, and CAPA activities.

Support laboratory inspections, audits, product transfers, and project work.

Maintain laboratory documentation, procedures, training records, and equipment compliance.

Act as a subject matter expert for analytical testing and laboratory operations.

Qualifications

Bachelor's degree in Analytical Chemistry or a related scientific discipline.

Minimum 4 years' analytical laboratory experience within the pharmaceutical industry.

Strong hands-on expertise in analytical techniques including HPLC, GC, LCMS, GCMS, titration, and identification methods.

Experience working in a GMP-regulated environment with strong knowledge of regulatory requirements and data integrity principles.

Previous leadership, supervisory, mentoring, or team coaching experience.

Experience supporting product or method transfers is an advantage.

Additional Information

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

Job details

Seniority
Not listed
Function
Quality
Therapeutic area
Not listed
Location
Sligo, SO
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 1008 comparable Quality roles across 131 biopharma companies.

1008Comparable roles tracked
957Currently active
131Companies hiring similar roles
48Countries represented

Salary context

193 of 1008 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 · Quality Control Stability Technician · Regeneron Pharmaceuticals, Inc (USA) $19/hr – $30/hr (≈ $39,395–$61,610/yr)
Highest disclosed · Quality Assurance Specialist · Merck KGaA $65,100/yr – $976,000/yr
Peer group range $50,502 – $520,550 (median $136,700)

Where these roles are based

Top locations among the 1008 comparable roles

United States350
Germany54
China53
Ireland52
Switzerland39
France38

+ 42 more countries

Seniority mix

498 of 1008 peers have a known seniority level

Manager160
Senior116
Intern/Fellow/Postdoc60
Associate Director40
Associate39
Director32
Principal23
Senior Director20
Executive/VP8

Therapeutic area mix

2 of 1008 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease1
Respiratory1

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
Mylan Teoranta Inverin, Ireland Manager
Same function Same country
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

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%
Microbiology Manager
Mylan Teoranta · Inverin, Ireland · Manager
Function Therapeutic area Seniority Country
40%
Director of Quality Assurance QP
Mylan Teoranta · Inverin, Ireland · Director
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.