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.
Location: Craigavon, Northern Ireland, UK
Hours: 37.5 per week, Mon-Fri with flexible working hours
Business Unit: Almac Sciences
Open To: Internal & External Applicants
Ref No.: HRJOB11539
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
Desirable Requirements:
- 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 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 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
Benefits:
- Staff Discounts
- Professional Coaching
- Attractive Compensation Package
- Employee Recognition Rewards for Years Of Service
- Group Healthcare Scheme
- Pension Scheme
Quality Compliance Team Leader TLNT1_NI in Craigavon employer: IrishJobs
Almac Sciences is an exceptional employer located in Craigavon, Northern Ireland, offering a dynamic work environment where innovation meets support. With a strong emphasis on professional development through coaching and mentoring, employees are encouraged to grow their skills while contributing to life-changing pharmaceutical solutions. The company also provides attractive benefits, including a competitive compensation package, healthcare schemes, and employee recognition rewards, making it a rewarding place to build a meaningful career.
StudySmarter Expert Advice🤫
We think this is how you could land Quality Compliance Team Leader TLNT1_NI 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 the interview by researching Almac Sciences and their quality compliance processes. Show us that you understand their mission and how your experience aligns with their goals. It’s all about making that connection!
✨Tip Number 3
Practice your answers to common interview questions, especially those related to QA and GMP. We want to see your expertise shine through, so be ready to share specific examples from your past experiences.
✨Tip Number 4
Don’t forget to follow up after your interview! A quick thank-you email can keep you fresh in the interviewer’s mind and show us that you’re genuinely interested in the role. Plus, it’s just good manners!
We think you need these skills to ace Quality Compliance Team Leader TLNT1_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 of Quality Compliance Team Leader. We want to see your relevant skills and achievements that match the job description.
Showcase Your Experience:When detailing your experience, focus on your QA/Compliance background in a pharmaceutical GMP environment. We’re looking for specifics, so don’t hold back on mentioning any significant projects or challenges you’ve tackled.
Be Clear and Concise:Keep your application clear and to the point. Use bullet points where possible to make it easy for us to read through your qualifications and experiences quickly. We appreciate straightforwardness!
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it gives you a chance to double-check everything before hitting send.
How to prepare for a job interview at IrishJobs
✨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 preparation for regulatory audits, especially from bodies like MHRA and FDA. Share any experiences you have in this area, highlighting how you contributed to successful audit outcomes.
✨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, such as your significant experience in reviewing manufacturing documentation and handling deviations.
