At a Glance
- Tasks: Ensure pharmaceutical batch records meet GMP standards and support timely batch release.
- Company: Almac Group is a leading pharmaceutical services company dedicated to quality and compliance.
- Benefits: Enjoy a competitive salary, flexible working hours, and opportunities for professional growth.
- Other info: Flexible working hours between 07:00 – 19:00 with core hours of 10:00 – 16:00.
- Why this job: Join a dynamic team focused on product quality and regulatory compliance in the healthcare sector.
- Qualifications: 5 GCSEs at grade C or above, 3 A-Levels, and experience in Quality Systems required.
The predicted salary is between 30000 - 42000 £ per year.
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The Role
The role focuses on ensuring pharmaceutical manufacturing and packaging batch records meet Good Manufacturing Practice (GMP) standards. The primary responsibility involves reviewing batch documentation for both commercial and clinical operations, preparing disposition packs for Qualified Person (QP) certification, and assessing any deviations or changes that could impact compliance. The post holder plays a key role in supporting timely batch release by aligning with On Time In Full (OTIF) delivery targets and managing electronic transactions to generate performance data.
Location: Craigavon
Hours: 37.5 hours per week
Salary: Competitive
Business Unit: Pharma Services
Open To: Internal & External Applicants
Ref No.: HRJOB10882
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The Role
The role focuses on ensuring pharmaceutical manufacturing and packaging batch records meet Good Manufacturing Practice (GMP) standards. The primary responsibility involves reviewing batch documentation for both commercial and clinical operations, preparing disposition packs for Qualified Person (QP) certification, and assessing any deviations or changes that could impact compliance. The post holder plays a key role in supporting timely batch release by aligning with On Time In Full (OTIF) delivery targets and managing electronic transactions to generate performance data.
In addition to core responsibilities, the role requires effective communication with internal and external stakeholders, ensuring queries are addressed professionally and promptly. The position also involves verifying data accuracy, supporting continuous improvement initiatives, and performing administrative tasks as needed. Overall, the role is integral to maintaining product quality and regulatory compliance throughout the batch release process.
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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
- 5 GCSE’s (or Equiv.) at grade C or above including English & Maths
- 3 A-Levels (or equiv.)
- Previous experience working within an established Quality System (e.g. GMP, ISO)
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.
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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 09 Sept 2025
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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 CV’s received or submitted directly to Hiring Managers will be considered unsolicited and no fee will be payable. Thank you for your cooperation.
Seniority level
Seniority level
Entry level
Employment type
Employment type
Full-time
Job function
Job function
Quality AssuranceIndustries
Pharmaceutical Manufacturing
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#J-18808-LjbffrProduct Quality Auditor in Craigavon employer: Almac Group
Almac Group is an exceptional employer, offering a dynamic work environment in Craigavon that prioritises employee growth and development within the pharmaceutical manufacturing sector. With a strong commitment to Good Manufacturing Practice (GMP) standards, employees benefit from a culture of continuous improvement, competitive salaries, and flexible working hours, all while contributing to meaningful projects that impact healthcare globally.
StudySmarter Expert Advice🤫
We think this is how you could land Product Quality Auditor in Craigavon
✨Tip Number 1
Familiarise yourself with Good Manufacturing Practice (GMP) standards, as this role heavily relies on compliance with these regulations. Understanding the nuances of GMP 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, especially those who work in quality assurance roles. Engaging with them can provide insights into the company culture at Almac Group and may even lead to referrals, increasing your chances of landing an interview.
✨Tip Number 3
Prepare to discuss specific examples from your past experiences that showcase your ability to manage batch documentation and handle deviations. Being able to articulate your problem-solving skills in real scenarios will set you apart from other candidates.
✨Tip Number 4
Stay updated on the latest trends and technologies in quality assurance within the pharmaceutical sector. Showing that you are proactive about continuous improvement and innovation can impress the hiring team and align with their goals for maintaining product quality.
We think you need these skills to ace Product Quality Auditor in Craigavon
Some tips for your application 🫡
Understand the Role:Before applying, make sure to thoroughly read the job description for the Product Quality Auditor position. Understand the key responsibilities, such as reviewing batch documentation and ensuring compliance with GMP standards.
Tailor Your CV:Customise your CV to highlight relevant experience in quality assurance and any previous work within established Quality Systems like GMP or ISO. Emphasise your educational qualifications, especially your GCSEs and A-Levels.
Craft a Strong Cover Letter:Write a compelling cover letter that addresses how your skills and experiences align with the requirements of the role. Mention your ability to communicate effectively with stakeholders and your commitment to maintaining product quality.
Proofread Your Application:Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. Ensure that all information is accurate and presented professionally, as attention to detail is crucial in this role.
How to prepare for a job interview at Almac Group
✨Understand GMP Standards
Familiarise yourself with Good Manufacturing Practice (GMP) standards, as this role heavily revolves around ensuring compliance. Be prepared to discuss how you have applied these standards in previous roles or how you would approach them in this position.
✨Showcase Your Attention to Detail
As a Product Quality Auditor, attention to detail is crucial. Prepare examples from your past experiences where your meticulous nature helped identify issues or improve processes. This will demonstrate your capability to manage batch documentation effectively.
✨Communicate Effectively
Effective communication with stakeholders is key in this role. Think of instances where you successfully communicated complex information to different audiences. Highlight your ability to address queries professionally and promptly during the interview.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your problem-solving skills and decision-making process. Practice articulating how you would handle deviations or changes that could impact compliance, showcasing your analytical thinking and adherence to quality standards.
