Find Quality Jobs in County Mayo

Supervisor, Laboratory Quality Control
AbbVie —Westport, County Mayo
- Full-time
- Analysis skills
- Supervising experience
- Bachelor's degree
Quality & Compliance Officer
Churchfield Home Services —County Mayo
- €35,000–€40,000 a year
- Full-time
- Writing skills
- Analysis skills
- No degree
- Annual leave
- Bereavement leave
Quick apply
6d
QC Analyst
Charles River Laboratories —Ballina, County Mayo
- Full-time
- Project management
- Annual leave
11d
QA CAPA/ NCR Governance Engineer
Vantive —Castlebar, County Mayo
- Analysis skills
- Manufacturing
- Communication skills
- Annual leave
- Employee assistance program
Lead Design Assurance Quality Engineer
Hollister Lietuva UAB —Ballina, County Mayo
- €3,100–€4,500 a month
- Hybrid work
- Microsoft Excel
- Assembly
- Project management
Quality Manager (Nursing)
Ethos Care Group —Ballina, County Mayo
- Leadership
- Communication skills
- Free parking
- Referral programme
Quick apply
11d

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The Grace Westport Estate —Westport, County Mayo
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Supervisor, Laboratory Quality Control

AbbVie -
Westport, County Mayo

Apply Now

Job details

Full-time

Qualifications

Analysis skills
Supervising experience
Bachelor's degree
Chemistry
Communication skills
Time management

Full job description

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

QC Pharma Supervisor

AbbVie is seeking a QC Pharma Supervisor to lead day-to-day Quality Control laboratory operations, supporting chemistry analysis and stability testing in line with defined schedules, regulatory requirements, and company standards.

About the Role
As QC Pharma Supervisor, you will supervise daily laboratory activities to ensure testing is completed accurately, on time, and in compliance with GMP/GLP and other applicable regulatory guidelines. You will support scheduling, participate in daily Tier 1 meetings, and work closely with Supervisors, Quality, and Laboratory Management to uphold the Quality Management System.

Key Responsibilities

Supervise daily laboratory operations and ensure team activities are carried out in compliance with regulatory requirements.
Support weekly and daily laboratory schedules and participate in daily Tier 1 meetings to review shift productivity.
Ensure all testing data, raw data, and results are documented accurately, legibly, and on time.
Use laboratory systems such as LIMS, Sample Manager, and Empower effectively.
Review and interpret test results.
Promote and maintain compliance with company standards in safety, housekeeping, and quality.
Identify and escalate any discrepancies or non-conformances to management.
Ensure good housekeeping and adherence to Good Laboratory Practices.
Work on a rotating monthly shift pattern.
Collaborate with team members, Supervisors, the Quality Manager, and the Laboratory Manager to ensure compliance with the Quality Management System.

Qualifications

BS in science or equivalent (Chemistry, Microbiology, or Biology preferred)
2-5 years of laboratory experience
2-5 years of supervisory experience
Demonstrated skills to deal effectively with members of the department and the areas serviced by the laboratory
Problem solving skills are required
Must be able to interpret impact of laboratory data for appropriate and effective actions
Must be able to identify problem areas requiring development, maintenance, production, engineering, accounting, or planning with assistance from more senior staff
Must also be able to identify, communicate, and follow-through to completion and assist in the development of necessary corrective action plans to resolve the problem with supervision. May also assist in the activities required for the investigation and resolution

Additional Information

Qualifications and Experience

Third-level qualification in a Science discipline, preferably Chemistry.
1–2 years’ experience working as an Analyst in a GMP/GLP environment.
1–2 years’ experience working with analytical equipment, particularly HPLC and GC, as well as other laboratory techniques.
Working knowledge and experience using Empower.
Strong understanding of Data Integrity from a laboratory perspective.
Excellent communication, organization, time management, and teamwork skills.
Demonstrated ability to work independently and take initiative.

Skills and Behaviours

Strong relationship-building skills and the ability to work effectively across functions.
Excellent verbal and written communication skills.
Strong planning, organising, and analytical skills.
Sound decision-making and problem-solving ability.
Adaptable and effective in a fast-paced, dynamic environment.
Results-driven, with a proactive and accountable approach.
Open to feedback and committed to continuous improvement.
A people-centered leadership style aligned with AbbVie’s values and culture.

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

Apply Now

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quality jobs in county mayo

Supervisor, Laboratory Quality Control

Quality & Compliance Officer

QC Analyst

QA CAPA/ NCR Governance Engineer

Lead Design Assurance Quality Engineer

Quality Manager (Nursing)

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