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- Tasks: Ensure quality and compliance of pharmaceutical products through monitoring and collaboration.
- Company: Join Almac Pharma Services, a leader in pharmaceutical quality assurance.
- Benefits: Enjoy flexible schedules, work-life balance, and free onsite parking.
- Other info: Hybrid working available after probation; must be flexible with hours.
- Why this job: Be part of a dynamic team improving healthcare while developing your skills in a supportive environment.
- Qualifications: Degree in Life Science or significant experience in the Pharmaceutical Industry required.
The predicted salary is between 36000 - 60000 £ 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 areasincluding manufacturing, quality control, product development, and distributionto 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 employer: Almac Group Ltd
Contact Detail:
Almac Group Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Specialist
✨Tip Number 1
Familiarise yourself with the specific regulatory requirements for pharmaceutical products, especially GMP and ISO standards. This knowledge will not only help you in interviews but also demonstrate your commitment to quality assurance.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, particularly those who work in quality assurance roles. Engaging with them can provide insights into the role and may even lead to referrals or recommendations.
✨Tip Number 3
Prepare to discuss your experience with quality systems and any specific projects you've worked on that relate to compliance and risk management. Being able to share concrete examples will set you apart from other candidates.
✨Tip Number 4
Stay updated on the latest trends and changes in pharmaceutical regulations. Showing that you are proactive about your professional development can impress potential employers and highlight your dedication to the field.
We think you need these skills to ace Quality Assurance Specialist
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to grasp the key responsibilities and requirements. Highlight your relevant experience in quality assurance, GMP compliance, and any specific knowledge of pharmaceutical regulations.
Tailor Your CV: Customise your CV to reflect how your skills and experiences align with the role of Quality Assurance Specialist. Emphasise your familiarity with quality systems, regulatory requirements, and any significant achievements in previous roles.
Craft a Strong Cover Letter: Write a compelling cover letter that outlines your motivation for applying and how you can contribute to Almac Pharma Services. Mention specific examples from your past work that demonstrate your expertise in quality assurance and compliance.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects attention to detail, which is crucial in quality assurance roles.
How to prepare for a job interview at Almac Group Ltd
✨Know Your GMP and Quality Systems
Make sure you have a solid understanding of Good Manufacturing Practice (GMP) and the quality systems relevant to the pharmaceutical industry. Be prepared to discuss your experience with these systems and how you've applied them in previous roles.
✨Showcase Your Problem-Solving Skills
Quality Assurance often involves addressing issues and implementing solutions. Think of specific examples where you've identified problems, developed corrective actions, and improved processes. This will demonstrate your proactive approach to quality management.
✨Familiarise Yourself with Regulatory Standards
Research the regulatory requirements for pharmaceutical products, especially those that are relevant to the role. Being able to discuss these standards confidently will show your commitment to compliance and quality assurance.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions during the interview that assess your decision-making and critical thinking skills. Practice articulating how you would handle specific situations related to quality assurance, such as managing deviations or conducting audits.