At a Glance
- Tasks: Ensure quality and compliance of pharmaceutical products while collaborating across departments.
- Company: Join Almac Pharma Services, a leader in the pharmaceutical industry.
- Benefits: Competitive salary, hybrid working options, and opportunities for professional growth.
- Other info: Flexible working hours with potential for hybrid work after probation.
- Why this job: Make a real impact on product quality and regulatory compliance in healthcare.
- Qualifications: Degree in Life Science or significant experience in the Pharmaceutical Industry required.
The predicted salary is between 30000 - 40000 € per year.
Location: Craigavon
Hours: 37.5 hours per week
Salary: Competitive
Business Unit: Pharma Services
Open To: Internal & External Applicants
Ref No.: HRJOB11469
The Role
The role focuses on ensuring and enhancing the quality and GMP (Good Manufacturing Practice) compliance of pharmaceutical products within Almac Pharma Services. The post holder will be responsible for monitoring and reviewing various operational areas including manufacturing, quality control, product development, and distribution to assess and maintain compliance with regulatory standards. They will provide expert quality assurance support across departments, collaborating with internal and external stakeholders to uphold product integrity and meet project timelines. In addition to oversight responsibilities, the post holder will actively contribute to the development and continuous improvement of quality systems such as deviation management, CAPA, change control, and risk assessments. They will participate in internal and external audits, review critical documentation, and support supplier management processes. The role also involves reviewing production and laboratory data, compiling product quality reviews, and serving as a key contact for compliance-related queries, all with the overarching goal of safeguarding the quality and regulatory compliance of pharmaceutical products.
Key Requirements
- Have eligibility to work in the UK OR possess a valid work permit that will allow you to take up full time employment in the UK
- Degree (or equivalent) in a Life Science or closely related field OR significant experience working within the Pharmaceutical Industry along with demonstrable knowledge may be considered as sufficient to meet educational requirements for this role.
- Significant experience working within an established Quality System (e.g. GMP, ISO)
- Comprehensive, working knowledge of the regulatory requirements for pharmaceutical products are essential, including familiarity with the principles of Good Manufacturing Practice, Pharmaceutical Quality Systems, Quality Risk Management and Pharmaceutical Product Lifecycles.
Further Information
The working pattern for this role is a flex pattern between the hours of 07:00 - 19:00 with core hours of 10:00 - 16:00. You will be eligible for hybrid working following the successful completion of probation. This role requires coverage beyond normal working hours on a regular basis and it is a condition of your employment that you are able to fulfil this requirement of the role.
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 13th May 2026.
RECRUITMENT AGENCIES PLEASE NOTE: Almac will only accept applications from agencies/business partners that have been invited to work on this role by our Talent Acquisition team. Speculative candidate CVs received or submitted directly to Hiring Managers will be considered unsolicited and no fee will be payable. Thank you for your cooperation.
Skills: Quality System Knowledge of GMP Pharmaceutical Manufacturing
Quality Assurance Specialist JBLE1_NI in Craigavon employer: Almac Group Ltd
Almac Pharma Services is an exceptional employer located in Craigavon, offering a dynamic work environment that prioritises quality and compliance in the pharmaceutical industry. With a strong commitment to employee development, we provide opportunities for growth through continuous training and hybrid working options post-probation, fostering a culture of collaboration and innovation. Our competitive salary and flexible working hours reflect our dedication to supporting our employees' work-life balance while ensuring they play a vital role in safeguarding product integrity.
StudySmarter Expert Advice🤫
We think this is how you could land Quality Assurance Specialist JBLE1_NI in Craigavon
✨Tip Number 1
Network like a pro! Reach out to people in the pharmaceutical industry, especially those who work in quality assurance. Attend industry events or webinars to make connections and learn about potential job openings.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GMP and quality systems. Be ready to discuss how your experience aligns with the role's requirements and share examples of how you've contributed to quality improvements in past positions.
✨Tip Number 3
Don’t just apply and wait! Follow up on your applications after a week or so. A quick email can show your enthusiasm and keep you on their radar. Plus, it’s a great way to ask if they need any more info from you.
✨Tip Number 4
Use our website to apply! Tailor your CV specifically for the Quality Assurance Specialist role, highlighting your relevant experience and skills. A well-crafted application can make all the difference in landing that interview.
We think you need these skills to ace Quality Assurance Specialist JBLE1_NI 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 criteria. We want to see your relevant skills and achievements that showcase your fit for the Quality Assurance Specialist position.
Showcase Your Knowledge:Don’t forget to emphasise your understanding of GMP and quality systems in your application. We’re looking for candidates who can demonstrate their expertise in regulatory requirements and quality assurance processes.
Be Clear and Concise:When writing your application, keep it straightforward and to the point. We appreciate clarity, so make sure your points are easy to read and directly related to the job description.
Apply Through Our Website:Remember to submit your application through our website! It’s the best way for us to receive your details and ensures you’re considered for the role. Plus, it makes the whole process smoother for everyone involved.
How to prepare for a job interview at Almac Group Ltd
✨Know Your GMP Inside Out
Make sure you brush up on Good Manufacturing Practice (GMP) principles before the interview. Be ready to discuss how you've applied these in your previous roles, as this will show your understanding of the regulatory landscape and your commitment to quality assurance.
✨Showcase Your Experience with Quality Systems
Prepare specific examples of your experience with established Quality Systems like ISO or CAPA. Highlight any improvements you've made or challenges you've overcome, as this demonstrates your proactive approach to quality management.
✨Be Ready for Scenario Questions
Expect scenario-based questions that assess your problem-solving skills in quality assurance. Think about past situations where you had to manage deviations or conduct risk assessments, and be prepared to explain your thought process and actions.
✨Engage with Stakeholders
Since collaboration is key in this role, think of examples where you've worked with internal or external stakeholders. Discuss how you ensured compliance and maintained product integrity, as this will show your ability to communicate effectively across departments.
