Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead a team ensuring quality compliance in pharmaceutical manufacturing.
- Company: Join Almac Sciences, a leader in life-changing pharmaceutical innovations.
- Benefits: Enjoy staff discounts, professional coaching, and an attractive compensation package.
- Other info: Flexible working hours and opportunities for continuous development.
- Why this job: Make a real impact in the pharmaceutical industry while advancing your career.
- Qualifications: Life sciences degree and significant QA/compliance experience in GMP environments.
The predicted salary is between 40000 - 50000 £ per year.
The post holder will lead a team of Quality Compliance professionals supporting manufacturing operations, ensuring timely delivery of GMP project support. The Quality Compliance Team Leader is responsible for QA approval and release of GMP products in line with internal procedures, while working closely with the wider quality function to maintain robust, compliant Quality Management Systems. A strong focus on coaching and mentoring will ensure team capability, performance, and continuous development.
Join Almac Sciences and be at the forefront of life-changing innovations. This is your chance to contribute to cutting-edge pharmaceutical solutions whilst advancing your own career in a supportive, forward-thinking environment.
Key Requirements- Life Sciences Degree level qualification
- Significant Experience of QA/Compliance within a Pharmaceutical GMP environment.
- Significant Experience of reviewing manufacturing documentation such as batch records and analytical data
- Significant Experience of investigation of Analytical and Manufacturing deviations
- Prior QA Manufacturing Support Experience Gained in a GMP API Company (CDMO or CRO) working to ICHQ7.
- Experience of preparation for regulatory audits (MHRA, FDA)
- Previous experience of supervising a team / leading a team
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 Wednesday 27th 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:- life science
- quality systems
- Pharma experience
- GMP Experience
- API manufacturing
- Staff Discounts
- Professional Coaching
- Attractive Compensation Package
- Employee Recognition Rewards for Years Of Service
- Group Healthcare Scheme
- Pension Scheme
Quality Compliance Team Leader in Craigavon employer: Almac Group Ltd
Contact Detail:
Almac Group Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Compliance Team Leader in Craigavon
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who work at Almac Sciences. A friendly chat can sometimes lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GMP and QA processes. We recommend practising common interview questions related to compliance and quality management systems to show you're the right fit for the Quality Compliance Team Leader role.
✨Tip Number 3
Showcase your leadership skills! Think of examples where you've coached or mentored others in your previous roles. This will highlight your capability to lead a team effectively, which is crucial for this position.
✨Tip Number 4
Don’t forget to apply through our website! Tailor your CV to reflect how your experience aligns with the job description. A well-crafted application can make all the difference in landing that interview.
We think you need these skills to ace Quality Compliance Team Leader in Craigavon
Some tips for your application 🫡
Tailor Your CV: Make sure to customise your CV to highlight how your experience aligns with the key requirements of the Quality Compliance Team Leader role. We want to see how your background in QA/Compliance and GMP environments makes you a perfect fit!
Showcase Your Achievements: Don’t just list your responsibilities; showcase your achievements! Use specific examples that demonstrate your impact in previous roles, especially in areas like team leadership and compliance management. This will help us see the value you can bring to our team.
Keep It Professional: While we love a friendly tone, remember to keep your application professional. Use clear language and avoid jargon unless it’s relevant to the role. This shows us you can communicate effectively in a professional setting.
Apply Through Our Website: We encourage you to apply through our website for a smooth application process. It’s the best way for us to receive your application and ensures you don’t miss any important updates about your application status!
How to prepare for a job interview at Almac Group Ltd
✨Know Your GMP Inside Out
Make sure you brush up on Good Manufacturing Practices (GMP) and how they apply to the pharmaceutical industry. Be ready to discuss your experience with QA compliance and how you've ensured adherence to these standards in previous roles.
✨Showcase Your Leadership Skills
As a Quality Compliance Team Leader, you'll need to demonstrate your ability to lead and mentor a team. Prepare examples of how you've successfully coached team members in the past and how you plan to foster their development in this role.
✨Be Audit-Ready
Familiarise yourself with the regulatory audit processes, especially those from MHRA and FDA. Be prepared to discuss your experience in preparing for audits and how you’ve handled any findings or deviations in the past.
✨Tailor Your CV and Answers
Before the interview, tailor your CV to highlight relevant experiences that match the job description. During the interview, align your answers with the key requirements, particularly your significant experience in reviewing manufacturing documentation and handling analytical deviations.