Global Quality Systems Senior Specialist

CompanyAlmac Group

LocationCraigavon, Northern Ireland, United Kingdom

Posted At1/22/2026

UK Visa Sponsorship Analytics

Occupation Type

IT business analysts, architects and systems designers

Occupation Code Skill LevelHigher Skilled

Sponsorship Salary Threshold

£54,900 (£28.15 per hour)

Occupation rate applies

Above analytics are generated algorithmically based on job titles and may not always be the same as the company's job classification. You can also check detailed occupation eligibility, and salary criteria on our UK Visa Eligible Occupations & Salary Thresholds page.

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Description

Location: Craigavon

Hours: 37.5 Hours

Salary: Competitive

Business Unit: Pharma Services

Open To: Internal & External Applicants

Ref No.: HRJOB11241

The Role:

The successful candidate will play a pivotal role in developing, implementing, and supporting electronic Quality Systems across our Global Pharma Services operations.

This is an exciting opportunity for an experienced quality professional who is passionate about system excellence, regulatory compliance, and driving continuous improvement on a global scale.

As a Global Quality Systems Senior Specialist, you will be instrumental in driving the design, implementation, validation and ongoing support of Quality Systems throughout our global network. Working closely with international sites, internal IS teams and external partners, you will act as a subject matter expert (SME) in Quality System architecture, Computer Systems Validation (CSV), and regulatory compliance.

You will support key projects, lead documentation and lifecycle activities, contribute to audits, and ensure that systems meet both business needs and industry standards.

Key Requirements:

Essential Criteria

Degree (or equivalent) in a Life Science or related discipline.
Significant experience working within a regulated Quality System (GMP, ISO, etc.).
Strong understanding of pharmaceutical quality system processes and regulatory requirements.
Knowledge of regulations governing computerised systems and control.

Desirable Criteria

(The following criteria may be applied if a large pool of applicants exist)

Experience writing detailed reports.
Experience in manufacturing/packaging of solid oral dosage forms.
Hands‑on CSV experience (writing, reviewing, executing validation documentation).

Apply Now

Apply online and tailor your CV to outline how you meet the role criteria. Please upload your CV in PDF format where possible.

Closing Date

We will no longer be accepting applications after 5pm on Friday 6th February 2026