Quality Assurance Team Leader (FTC: 9 months)
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Quality Assurance Team Leader (FTC: 9 months)
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Almac Group Quality Assurance Team Leader (FTC: 9 months)
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Quality Assurance Team Leader (FTC: 9 months)
role at
Almac Group Get AI-powered advice on this job and more exclusive features. Quality Assurance Team Leader (FTC: 9 months)
Location:
Craigavon
Hours:
37.5 hours per week
Salary:
Competitive
Business Unit : Pharma Services
Open To : Internal & External Applicants
Internal Applicants : A secondment will be considered for this role if agreed to by your current Line Manager.
Ref No.:
HRJOB10620
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The Role
Are you ready to lead a dynamic team at the forefront of pharmaceutical quality assurance?
We’re seeking an experienced and driven Quality Assurance Team Leader to head a multidisciplinary team of QA Specialists, Coordinators. In this pivotal role, you’ll ensure compliance with GMP principles and the Pharmaceutical Quality System while supporting manufacturing and packaging operations.
You will oversee critical quality systems including change management, deviation handling, stability documentation, and product complaints—ensuring timely, compliant, and effective outcomes that safeguard product integrity and patient safety.
The QA Team Leader is a key contact for internal teams and external stakeholders, guiding investigations, presenting to regulatory bodies, and mentoring your team to deliver excellence. If you’re passionate about quality, thrive in a fast-paced environment, and want to make a tangible impact in pharmaceutical services, we’d love to hear from you.
Full details of the job role can be found in the Job Description attached at the bottom of this job advert.
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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 science, life science or technical discipline or closely related field OR significant relevant work experience and knowledge will be considered in lieu of degree GCSE English and Mathematics or equivalent (Grade C or above) Experience working within an established Quality System within the Pharmaceutical Industry. Experience in leading a team of quality professionals. Experience of solid oral dosage forms in development scale including clinical supply, and commercial scale manufacture. Knowledge on Root Cause Analysis technique
Please note further desirable criteria contained within the Job Description attached at the bottom of the job advert.
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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 also be eligible for hybrid working following the successful completion of probation.
This role may require travel and coverage beyond normal working hours as and when required. It is a condition of your employment that you can fulfil this element of the role
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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.
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Closing Date
We will no longer be accepting applications after 5pm on
20 Jun 2025
ㅤ Seniority level
Seniority level Mid-Senior level Employment type
Employment type Full-time Job function
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