At a Glance
- Tasks: Support global regulatory compliance and monitor pharmaceutical legislation changes.
- Company: Join Almac Group, a leader in advancing human health globally.
- Benefits: Competitive salary, generous holiday allowance, healthcare reimbursement, and professional development opportunities.
- Other info: Flexible schedules, wellness programs, and opportunities for career advancement.
- Why this job: Make a real impact on patient safety and global regulatory compliance.
- Qualifications: GCSEs in English and Maths, experience in Quality roles, and knowledge of pharmaceutical legislation.
The predicted salary is between 35000 - 45000 £ per year.
Almac Group is a global leader in advancing human health. We provide a range of expert services across the drug development lifecycle to pharmaceutical and biotech companies, supporting them in finding treatments for patients.
Location: Craigavon
Hours: 37.5 hours per week
Salary: Competitive plus excellent benefits package
Business Unit: Almac Pharma Services
Ref No.: HRJOB11388/1
The Role
Almac Pharma Services is a global contract development and manufacturing organisation, providing integrated pharmaceutical services to clients worldwide. Quality is central to everything we do, ensuring safe, compliant and effective medicines reach patients across global markets. We are currently seeking a Global Quality Specialist (Regulatory Compliance) to join our Global Quality Assurance team in Craigavon. In this role, you will play a key part in supporting the global regulatory intelligence programme, monitoring new and evolving pharmaceutical legislation and ensuring the wider business is informed, prepared and compliant. You will work closely with global stakeholders, supporting risk management and change implementation in response to regulatory updates across multiple territories. This is an excellent opportunity for a quality professional with strong regulatory knowledge to develop their career within a global organisation.
Key Responsibilities
- Support the management of the global regulatory intelligence programme, monitoring regulatory news, legislative updates, warnings, guidance changes and inspection findings.
- Communicate emerging regulatory requirements and changes across the organisation, supporting awareness and compliance.
- Assist with compliance risk assessments against global pharmaceutical regulations, ensuring regulatory changes are reviewed and implemented ahead of effective dates.
- Support impact assessments for changes in legislation and assist with updates to internal processes where required.
- Support the management and maintenance of global site licences.
- Assist with client regulatory filing support requests, ensuring timely and accurate responses.
- Support the generation of regulatory newsletters and communications for the wider global business.
- Contribute to the Quality Mission and Vision, ensuring quality excellence and continuous improvement.
- Provide support to additional quality initiatives and projects as required.
This role requires regular coverage beyond normal working hours and flexibility is a condition of employment.
Quality & Compliance
- Ensure GMP compliance in all aspects of work.
- Engage actively with the Pharmaceutical Quality System to ensure accurate, timely completion of quality records.
- Support business objectives through strong quality performance and proactive risk management.
- Maintain a high standard of documentation, accuracy and attention to detail.
Key Requirements
- 5 GCSEs (or equivalent) at Grade C or above, including English and Maths.
- Level 5 qualification or significant experience within the Pharmaceutical Industry in lieu of qualification.
- Experience working in a Quality role within the Pharmaceutical Industry.
- Working knowledge of pharmaceutical legislation relating to the manufacture and distribution of medicines.
- Proficiency in IT applications (Word, Excel, Outlook, PowerPoint, etc.).
- Bachelor’s degree (or above) in a scientific or technical discipline (e.g. Chemistry, Biology, Pharmacy, Engineering).
- Experience in Regulatory Compliance activities.
- Knowledge of EU and US pharmaceutical legislation.
- Awareness of regulatory requirements from Rest of World territories.
Reward
A competitive salary and benefits package is available, including annual bonus, generous holiday allowance, healthcare reimbursement scheme, and the opportunity to work in a role that has a direct impact on patient safety and global regulatory compliance.
Apply Now
Apply online by uploading your CV (PDF format preferred). Please ensure your application clearly demonstrates how you meet the essential criteria outlined above. Closing Date – 5pm Tuesday 28th July 2026.
Almac Group is an Equal Opportunity Employer.
Global Quality Specialist (Regulatory Compliance) in Craigavon employer: OASIS Group
Almac Group is an exceptional employer, offering Software Engineer opportunities that allow you to contribute to meaningful projects in the healthcare sector. With a strong focus on collaboration and professional development, employees benefit from a supportive work culture that values innovation and integrity, all while working with cutting-edge technologies in a global organisation dedicated to advancing human health.
StudySmarter Expert Advice🤫
We think this is how you could land Global Quality Specialist (Regulatory Compliance) in Craigavon
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like OASIS Group. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
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Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like OASIS Group.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like OASIS Group. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
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When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what OASIS Group is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Global Quality Specialist (Regulatory Compliance) in Craigavon
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at OASIS Group!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show OASIS Group that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at OASIS Group!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At OASIS Group, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at OASIS Group
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at OASIS Group that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with OASIS Group’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
