Find Lead pharmaceutical Jobs in Dublin, D

QC Analyst
Alexion Pharmaceuticals,Inc. —Dublin, County Dublin
3d
QC Analyst
AstraZeneca —Dublin, County Dublin
3d
Analyst
Aon Corporation —Dublin, County Dublin
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- Full-time
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MS&T Process Chemist
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Jazz Pharmaceuticals —Dublin, County Dublin
- Master's degree
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- Annual leave
4d
EAP Program Manager
Uniphar Durbin Ireland Limited —Rathcoole, County Dublin
- Full-time
- Hybrid work
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- Employee assistance program
Quick apply
Lab Apprentice
Mallinckrodt —Dublin, County Dublin
- Full-time
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Scientific Engagement & Program Manager
Novartis —Dublin, County Dublin
- Full-time
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Senior Business Development Manager
Heterochem Dist Ltd —Baldoyle, County Dublin
- €75,000–€90,000 a year
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Quality Operations Team Lead
United Drug —Dublin, County Dublin
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Manager, Life Sciences - Dublin
Gate One —Dublin, County Dublin
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Buyer/Sourcing Specialist
CEC —Dublin, County Dublin
- Full-time
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Regional Quality Lead
Rockwell Engineering —Dublin, County Dublin
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EHS Advisor
PJ Hegarty & Sons —Dublin, County Dublin
- Full-time
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1d
Expanded Access Program Coordinator Team Lead
Uniphar Durbin Ireland Limited —DUBLIN 24, County Dublin
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3d
Manager, Regulatory Affairs
Azurity Pharmaceuticals - Ireland —Dublin, County Dublin
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EMEA Account Lead
JLL —Dublin, County Dublin
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QC Analyst

Alexion Pharmaceuticals,Inc. -
Dublin, County Dublin

Apply Now

Job details

3 days ago

Full job description

Location: Dublin, Ireland

Job reference: R-254117

Date posted: 06/09/2026

This is what you will do:

The individual in this position should have a working knowledge of the cGMP QC laboratory environment and laboratory equipment associated with microbiological analysis. The QC Microbiology Analyst is responsible for testing using Micro techniques, performing Environmental Monitoring and compilation of Trends in Alexion Dublin. The position requires the ability to understand and follow written SOPs, to accurately and legibly record work in real time, and pay close attention to detail. The individual must be able to perform routine tasks with a minimum of supervision.

You will be responsible for:

Environmental and Facilities monitoring sampling and testing.

Testing to support release and stability programs on site.

Ensuring high cGMP, GLP standards are maintained while testing and adherence to schedules and targets to meet regulatory and business requirements.

To ensure a high standard of housekeeping and safety is maintained in the Laboratory.

Completion of project work and implementation of initiatives designed to improve the efficiency of the laboratory function/department.

To keep management updated on issues arising within the laboratory.

Investigate out of specification/limit results utilizing Structured Problem Solving, Root Cause Analysis tools in conjunction with the Microbiology Laboratory Supervisor, QA and other relevant departments and to implement effective corrective and preventative actions while ensuring all investigations are closed with the specified lead-time.

To train laboratory personnel and play appropriate role in the development, operation and evaluation of training/re-training programs.

You will need to have

Minimum of 1 year experience in cGMP Quality environment.

Experience in testing of sterile/non-sterile pharmaceutical /biopharmaceutical products.

Good knowledge of current regulatory requirements for Microbiology / Sterility Assurance in support of cGMP operations supporting clinical and commercial manufacturing.

Degree in Microbiology or related science.

The duties of this role are generally conducted in an lab environment. As is typical of a lab-based role, employees must be able, with or without an accommodation to: lift/carry 15/30 pounds unassisted/assisted; work comfortably in a controlled environment with and around biological, infectious, and hazardous materials; gown/degown PPE; use a computer; engage in communications via phone, video, and electronic messaging; engage in problem solving and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours.

We would prefer for you to have:

Experience/Knowledge of aseptic techniques

Date Posted

09-Jun-2026

Closing Date

22-Jun-2026Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.

Apply Now

Refine Your Search

lead pharmaceutical jobs in dublin, d

QC Analyst

QC Analyst

Analyst

Publishing & Content Management Specialist

Strategic Assistant

Medical Science Liaison

MS&T Process Chemist

Quality Control Specialist

EAP Program Manager

Lab Apprentice

Scientific Engagement & Program Manager

Senior Business Development Manager

Quality Operations Team Lead

Manager, Life Sciences - Dublin

Buyer/Sourcing Specialist

Regional Quality Lead

EHS Advisor

Expanded Access Program Coordinator Team Lead

Manager, Regulatory Affairs

EMEA Account Lead

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