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- Tasks: Ensure quality standards in drug manufacturing and support the QA team with audits and training.
- Company: Curia, a global leader in drug development and manufacturing solutions.
- Benefits: Flexible hours, competitive salary, health benefits, and generous pension contributions.
- Other info: Opportunity for career growth and involvement in continuous improvement projects.
- Why this job: Join a dynamic team and make a real impact in the pharmaceutical industry.
- Qualifications: Science-related qualification and 2+ years of QA experience in a GMP environment.
The predicted salary is between 30000 - 40000 £ per year.
Curia is a leading global provider of advanced drug development, contract research and manufacturing solutions to the pharmaceutical and biotechnology industries. We have a fantastic opportunity at Curia Glasgow for an experienced Quality Assurance Specialist to join our team.
If you have 2 years+ QA experience gained within a similar GMP drug manufacturing pharma environment and have a dedicated and thorough work ethic, then we would very much like to hear from you.
You will also be required to provide advice for departments based on GMP and scientific rationale, and at times this will be on a paid 'On call' basis. With your knowledge and experience you will be able to review and progress deviations, complaints, investigations, CA/PA in reasonable time frames whilst maintaining your attention to detail.
Working as part of a small team, this is a technical position with responsibility for providing a support function to the QA team and ensuring this work is performed in an organised and timely manner. In addition, this role will perform administrative and technical Quality Assurance duties, whilst adhering to GMP, COSHH and Health and Safety regulations.
Responsibilities include:
- Providing feedback/corrections to authors and escalating concerns to the Quality Manager/Head of Quality where necessary.
- Representing Quality Assurance in continuous improvement projects ensuring that change is performed in accordance with GMP, site procedures and industry regulations and guidelines.
- Assisting in the performance of supplier audits, supporting the Lead Auditor.
- Acting as a support to client and regulatory audits, helping with technical support to the audit team and responding to requests for documentation and information.
- Working to a schedule as defined by the Quality Manager/Head of Quality.
- Conducting self-inspections/audits to ensure compliance with Quality Management System procedures and GMP regulations.
- Ensuring timely and effective communication and escalation of quality issues to the appropriate levels of management.
- Carrying out training for QMS activities as defined by line management.
Therefore the Quality Specialist must:
- Hold a Science related qualification, degree or a minimum of HND level with QA experience.
- Have proven experience within a similar Quality manufacturing environment.
- Have a clear understanding of regulatory commitments, e.g. GMP, ICH, COSHH as well as practical experience of GMP procedures, facilities and methods.
- Remain aware of workload levels and priorities within the QA team/other departments and communicate these to senior management in a timely fashion where necessary.
Hours - 37.5 (flexible start/finish times)
Quality Specialist - Training in Glasgow employer: Curia
Contact Detail:
Curia Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Specialist - Training in Glasgow
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical and biotech industries. Attend industry events or webinars, and don’t be shy about introducing yourself. You never know who might have the inside scoop on job openings!
✨Tip Number 2
Prepare for interviews by brushing up on GMP regulations and quality assurance practices. We recommend doing mock interviews with friends or using online platforms to get comfortable with common questions. The more you practice, the more confident you'll feel!
✨Tip Number 3
Showcase your experience! When you get the chance to chat with potential employers, highlight your past QA roles and how you've contributed to compliance and improvements. Use specific examples to demonstrate your skills and knowledge.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search. So, go ahead and submit your application today!
We think you need these skills to ace Quality Specialist - Training in Glasgow
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Quality Specialist role. Highlight your QA experience, especially in GMP environments, and showcase any relevant qualifications. We want to see how your background aligns with what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality assurance and how your skills can benefit our team. Keep it concise but impactful – we love a good story!
Showcase Your Attention to Detail: In QA, attention to detail is key. Make sure your application is free from typos and errors. We appreciate candidates who take the time to present their work neatly and professionally – it reflects your commitment to quality!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just follow the prompts and submit your materials!
How to prepare for a job interview at Curia
✨Know Your GMP Inside Out
Make sure you brush up on your Good Manufacturing Practice (GMP) knowledge before the interview. Be ready to discuss how you've applied GMP in your previous roles, and think of specific examples where you ensured compliance or improved processes.
✨Showcase Your Attention to Detail
As a Quality Specialist, attention to detail is crucial. Prepare to share instances where your meticulous nature helped identify issues or improve quality. This could be anything from reviewing documentation to conducting audits.
✨Prepare for Technical Questions
Expect technical questions related to Quality Assurance and regulatory commitments. Familiarise yourself with ICH and COSHH regulations, and be ready to explain how you've navigated these in past roles. It’s all about demonstrating your expertise!
✨Communicate Effectively
Since this role involves liaising with various departments, practice articulating your thoughts clearly. Think about how you would communicate quality issues or improvements to non-technical staff. Good communication can set you apart!