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For Companies At a Glance
- Tasks: Drive the design and support of electronic Quality Systems in a global pharma environment.
- Company: Join a leading global Pharma Services company with a focus on quality and compliance.
- Benefits: Competitive salary, flexible hours, and opportunities for professional growth.
- Why this job: Make a real impact on global quality systems and enhance your career in the pharmaceutical industry.
- Qualifications: Degree in Life Science and experience in regulated Quality Systems required.
- Other info: Collaborative environment with international exposure and excellent career advancement opportunities.
The predicted salary is between 36000 - 60000 £ per year.
The successful candidate will play a pivotal role in developing, implementing, and supporting electronic Quality Systems across our Global Pharma Services operations.
Location: Craigavon
Hours: 37.5 Hours
Salary: Competitive
Business Unit: Pharma Services
Open To: Internal & External Applicants
Ref No.: HRJOB11241
Responsibilities
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. You will work closely with international sites, internal IS teams and external partners, and 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
- Experience writing detailed reports.
- Experience in manufacturing/packaging of solid oral dosage forms.
- Hands‑on CSV experience (writing, reviewing, executing validation documentation).
Apply
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.
Global Quality Systems Senior Specialist in Craigavon employer: Almac Group
Contact Detail:
Almac Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Global Quality Systems Senior Specialist in Craigavon
✨Tip Number 1
Network like a pro! Reach out to current employees in the company or industry on LinkedIn. A friendly chat can give us insider info and might even lead to a referral.
✨Tip Number 2
Prepare for the interview by researching the company’s quality systems and recent projects. We want to show that we’re not just interested, but genuinely excited about what they do!
✨Tip Number 3
Practice common interview questions related to Quality Systems and regulatory compliance. We can even role-play with a friend to boost our confidence and refine our answers.
✨Tip Number 4
Don’t forget to follow up after the interview! A quick thank-you email can keep us fresh in their minds and shows our enthusiasm for the role.
We think you need these skills to ace Global Quality Systems Senior Specialist in Craigavon
Some tips for your application 🫡
Tailor Your CV: Make sure to customise your CV to highlight how your experience aligns with the role of Global Quality Systems Senior Specialist. We want to see your relevant skills and achievements that match the job description!
Showcase Your Experience: When detailing your experience, focus on your work within regulated Quality Systems and any hands-on CSV experience you have. We love seeing specific examples that demonstrate your expertise in pharmaceutical quality processes.
Be Clear and Concise: Keep your application clear and to the point. Use bullet points where possible to make it easy for us to read through your qualifications and experiences. We appreciate a well-structured application!
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy to upload your CV in PDF format there.
How to prepare for a job interview at Almac Group
✨Know Your Quality Systems
Make sure you brush up on your knowledge of electronic Quality Systems and Computer Systems Validation (CSV). Be ready to discuss specific examples from your past experience that demonstrate your understanding of these systems and how they align with regulatory compliance.
✨Showcase Your Collaboration Skills
Since this role involves working closely with international sites and internal teams, prepare to share examples of how you've successfully collaborated in the past. Highlight any cross-functional projects you've been part of and how you navigated challenges with external partners.
✨Prepare for Technical Questions
Expect technical questions related to pharmaceutical quality system processes and regulations. Review key regulations governing computerised systems and be ready to explain how you've applied these in your previous roles. This will show your expertise and readiness for the position.
✨Tailor Your CV and Examples
Before the interview, ensure your CV is tailored to highlight relevant experience in regulated Quality Systems. Prepare specific examples that showcase your hands-on CSV experience and your ability to write and review validation documentation, as these are crucial for the role.
