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- Tasks: Join our QA team to ensure compliance and improve manufacturing processes.
- Company: We're a leading pharmaceutical company based in Wrexham, committed to quality and innovation.
- Benefits: Enjoy a permanent role with 24/7 shifts and opportunities for professional growth.
- Why this job: Be part of a dynamic team making a real impact in the pharmaceutical industry.
- Qualifications: Ideal candidates have a BSc in science or relevant experience in Quality Assurance.
- Other info: No recruitment fees; apply now to kickstart your career!
The predicted salary is between 30000 - 42000 £ per year.
We are actively recruiting for a Quality Assurance (QA) Officer to join our Client's dynamic QA Operations Team. This permanent position is located at their Wrexham site in North Wales and will report directly to the QA Process Leader. The role involves working on a 24/7 shift basis.
Main Duties:
- Support improvements to optimise departmental performance (efficiency and compliance).
- Support improvements in site processing practices.
- Perform assigned tasks whilst always adhering to current GMP requirements.
- Report any compliance concerns to your line-manager.
- Perform Quality review of all batch documentation in all site manufacturing facilities to ensure compliance to regulatory requirements and business lead times.
- Provide general input/solutions based on knowledge of GMP, QRM and an understanding of batch processing.
- Provide Quality input for general non-conformances, out of specifications, change control and CAPA in line with current Quality Compliance procedures.
- Escalate complex and/or critical activities to next level.
Main Responsibilities:
- You will be responsible for the review and approval of batch documentation to support the QPs in certification of site manufactured batches and release in accordance with EU regulatory requirements.
- Provide Quality Oversight across manufacturing streams utilising knowledge of cGMP regulatory guidelines, and industry standards.
- Participate in Quality Management Processes: Unplanned Events, Complaints, Corrective/Preventive Actions (CAPA), Change Control, Product Recall, Blue Mountain, SAP and other site systems as required to identify and support improvements in site practices.
- Support routine operational activities and continuous improvements associated with site manufacturing activities.
The successful applicant will have sound knowledge of cGMP and QRM relating to aseptic manufacturing and will be organised with a good sense of prioritisation, time and risk management techniques plus able to communicate and facilitate the operation of systems within Quality.
Our Client is also looking for candidates who have:
- Ideal: BSc in a science discipline.
- Minimum: A levels/equivalent, including a science subject or evidence of science-based education/training.
- Experience: Ideal: 3+ years pharmaceutical experience in sterile manufacturing of which more than 1 year in Quality Assurance. Minimum: 1+ year in pharmaceutical manufacturing in a Quality role.
If this sounds like the role for you - Please call us NOW to discuss further!
QA Officer in Wrexham employer: Saske Recruitment
Contact Detail:
Saske Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QA Officer in Wrexham
✨Tip Number 1
Familiarise yourself with current Good Manufacturing Practices (cGMP) and Quality Risk Management (QRM) principles. Understanding these concepts will not only help you in the interview but also demonstrate your commitment to quality assurance in the pharmaceutical industry.
✨Tip Number 2
Network with professionals in the pharmaceutical sector, especially those working in quality assurance roles. Engaging with industry contacts can provide insights into the company culture and expectations, which can be invaluable during your application process.
✨Tip Number 3
Prepare to discuss specific examples from your past experience that showcase your ability to handle compliance issues and improve operational efficiency. Being able to articulate your contributions to previous roles will set you apart from other candidates.
✨Tip Number 4
Research the company’s recent projects or initiatives related to quality assurance. Showing that you are informed about their work and how you can contribute will demonstrate your genuine interest in the role and the organisation.
We think you need these skills to ace QA Officer in Wrexham
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to understand the responsibilities and requirements of the QA Officer position. Highlight key skills and experiences that align with the role.
Tailor Your CV: Customise your CV to reflect your relevant experience in Quality Assurance and pharmaceutical manufacturing. Emphasise your knowledge of cGMP and QRM, and include specific examples of your achievements in previous roles.
Craft a Compelling Cover Letter: Write a cover letter that addresses why you are a great fit for the QA Officer position. Mention your understanding of GMP requirements and your ability to support continuous improvements in site practices.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. Ensure that all information is clear and professional, as attention to detail is crucial in Quality Assurance.
How to prepare for a job interview at Saske Recruitment
✨Know Your GMP and QRM
Make sure you brush up on your knowledge of current Good Manufacturing Practices (cGMP) and Quality Risk Management (QRM). Be prepared to discuss how these principles apply to the role and provide examples from your past experience.
✨Demonstrate Your Problem-Solving Skills
The role involves addressing compliance concerns and non-conformances. Think of specific instances where you've successfully identified issues and implemented solutions, and be ready to share these during the interview.
✨Showcase Your Teamwork Abilities
As a QA Officer, you'll be working closely with various teams. Highlight your experience in collaborative environments and how you’ve contributed to team success, especially in quality management processes.
✨Prepare Questions About the Role
Have a few insightful questions ready about the company's quality assurance practices and how they handle continuous improvement. This shows your genuine interest in the position and helps you assess if it's the right fit for you.
