Quality Assurance Specialist
Quality Assurance Specialist

Quality Assurance Specialist

Full-Time 30000 - 40000 £ / year (est.) Home office (partial)
Almac Group Ltd

At a Glance

  • Tasks: Ensure quality and compliance of pharmaceutical products while collaborating with various teams.
  • 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 relevant experience in the Pharmaceutical Industry required.

The predicted salary is between 30000 - 40000 £ per year.

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

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

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 collaboration across departments, fostering a culture of innovation and excellence. Our competitive salary and flexible working arrangements, including hybrid options post-probation, make Almac an attractive choice for those seeking meaningful and rewarding careers in quality assurance.
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

Network like a pro! Reach out to folks in the pharmaceutical industry, especially those who work in quality assurance. A friendly chat can lead to insider info about job openings and even referrals.

✨Tip Number 2

Prepare for interviews by brushing up on GMP and quality systems. We want you to showcase your knowledge and experience confidently. Practice common interview questions and think of examples that highlight your skills.

✨Tip Number 3

Don’t forget to follow up after interviews! A quick thank-you email can keep you fresh in the interviewer’s mind and show your enthusiasm for the role. Plus, it’s just good manners!

✨Tip Number 4

Apply through our website! It’s the best way to ensure your application gets seen. Tailor your CV to highlight your relevant experience in quality assurance and GMP compliance to stand out from the crowd.

We think you need these skills to ace Quality Assurance Specialist

Quality Assurance
Good Manufacturing Practice (GMP)
Regulatory Compliance
Pharmaceutical Quality Systems
Quality Risk Management
Deviation Management
Corrective and Preventive Actions (CAPA)
Change Control
Risk Assessments
Internal and External Audits
Data Review
Collaboration Skills
Communication Skills
Problem-Solving Skills

Some tips for your application 🫡

Tailor Your CV: Make sure to customise your CV to highlight how your experience aligns with the role of Quality Assurance Specialist. We want to see your relevant skills and achievements that match the job description.

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 role.

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’s super easy!

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 any other relevant frameworks. Highlight how you've contributed to quality improvements or compliance in past positions, as this will demonstrate your hands-on knowledge and problem-solving skills.

✨Familiarise Yourself with Regulatory Requirements

Research the key regulatory requirements for pharmaceutical products. Being able to discuss these confidently will not only impress your interviewers but also show that you're proactive about staying informed in a constantly evolving industry.

✨Prepare Questions for Your Interviewers

Think of insightful questions to ask during the interview. This could be about their quality systems, team dynamics, or upcoming projects. It shows your genuine interest in the role and helps you assess if the company is the right fit for you.

Quality Assurance Specialist
Almac Group Ltd

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