Find pharmaceutical Jobs in county kildare

QA Specialist
Abacus Medicine Group —Kildare, County Kildare
- English
7d
QA Specialist
Abacus Medicine —Naas, County Kildare
- Full-time
- English
7d
Field Service Engineer
Printscan Support Services Ltd —Celbridge, County Kildare
- €30,000–€40,000 a year
- Full-time
- Communication skills
Quick apply
9d
Business Intelligence & Digital Systems Administrator – Construction Quality
DPS Group —Kildare, County Kildare
- Engineering
- Bachelor's degree
- Construction
Field Service Engineer
Life Sciences Ireland and UK —Kildare, County Kildare
- Full-time
- Maintenance
- No degree
Quick apply
OTC Pharmacy Sales Assistant - part-time- Maynooth
McCartan's Pharmacy —Maynooth, County Kildare
- Part-time
- Customer service
- Communication skills
Quick apply
6d
Sales Specialist
IQVIA —Kildare, County Kildare
- Full-time
- Business
- Communication skills
- Annual leave
6d
Senior Mechanical Project Engineer
Leo Lynch —Kildare, County Kildare
- Full-time
- Analysis skills
- Project management
- Communication skills
Quick apply

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QA Specialist

Abacus Medicine Group
Kildare, County Kildare

Apply Now

Job details

7 days ago

Qualifications

English
Quality assurance

Full job description

Do you want to play a key role in ensuring quality and compliance across pharmaceutical operations in Europe? Join a growing international pharmaceutical company where quality is not just about documentation – but about supporting operations, improving processes, and safeguarding patient safety.

This is an opportunity to step into a broad QA role with both operational and strategic responsibilities, working closely with the Responsible Person and cross-functional stakeholders across the business.

The opportunity

You will join our Quality Assurance team and become part of an international environment where collaboration, ownership, and continuous improvement are highly valued.

In this role, you will work closely with the Responsible Person and support a wide range of quality activities across the business. The position combines hands-on operational QA work with process improvements and compliance oversight, giving you broad exposure to pharmaceutical quality systems and distribution activities.

The team works in a collaborative and pragmatic way, where quality is seen as a business partner to operations. You will have the opportunity to contribute actively to investigations, CAPAs, audits, documentation reviews, and continuous improvement initiatives while supporting compliance with GDP requirements and internal quality standards.

Your responsibilities will include:

Supporting the maintenance and continuous improvement of the Quality Management System (QMS)
Managing and tracking quality documentation including SOPs, investigations, CAPAs, deviations, protocols, and change controls
Assisting with investigations, root cause analysis, and corrective and preventive actions (CAPAs)
Tracking and trending quality metrics and supporting monthly quality reporting
Performing quality review of documentation and operational processes
Participating in batch documentation review to support timely quality release activities
Supporting risk assessments related to product quality, safety, and compliance
Assisting with change control activities and document archival
Performing routine audits and gap assessments across processes and documentation
Supporting SOP revisions and participating in inspections when needed
Collaborating cross-functionally with operational and quality stakeholders across the business

We would like you to:

Take ownership of quality tasks and follow them through with a structured and proactive mindset
Support continuous improvement of quality processes and systems
Work closely with operational teams while maintaining a strong quality focus
Contribute to investigations, audits, and compliance activities in a pragmatic and solution-oriented way
Help ensure high quality standards across documentation, processes, and daily operations

What we need you to have:

Experience within Quality Assurance in the pharmaceutical industry
Knowledge of GDP and/or GMP requirements
Experience working with investigations, deviations, CAPAs, and quality documentation
A structured and detail-oriented approach combined with strong collaboration skills
Professional proficiency in English

It is an advantage if you also have experience supporting audits, inspections, or batch documentation review.

What we offer:

A broad and impactful QA role in an international pharmaceutical company
The opportunity to work closely with experienced QA and Responsible Person professionals
A collaborative and informal work environment with high professional standards
Opportunities for professional and personal development
A company culture focused on trust, ownership, and continuous improvement

Are you interested?

If you want to apply, please use the apply link and attach your resumé.

We look forward to receiving your application!

Moving Healthcare. Moving You.

In Abacus Medicine Group, you’ll experience the power of Moving Healthcare. With our change mindset, we're moving the industry and improving healthcare as we broaden access to medicine.

But it's not just about moving healthcare, it's about Moving You. You’ll be part of a caring community of more than 1,800 people across the World. With us, you will be valued, empowered, and have a direct impact on driving change. Let's access the future of medicine and make a difference together. Your move.

Do you want to know about us?

Follow us on Instagram and LinkedIn and get an insight into everyday life at Abacus Medicine. For job openings, check our Career page.

Apply Now

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