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- Tasks: Ensure quality in drug manufacturing and support the QA team with audits and compliance.
- Company: Curia, a global leader in drug development and manufacturing solutions.
- Benefits: Flexible hours, competitive salary, health benefits, gym membership, and generous pension contributions.
- Other info: Opportunity for career growth and involvement in continuous improvement projects.
- Why this job: Join a dynamic team making a real difference in pharmaceutical quality assurance.
- 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. Provides feedback/corrections to authors and escalates concerns to the Quality Manager/Head of Quality where necessary.
Represent Quality Assurance in continuous improvement projects ensuring that change is performed in accordance with GMP, site procedures and industry regulations and guidelines. Assists in the performance of supplier audits, supporting the Lead Auditor. Acts as a support to client and regulatory audits, helping with technical support to the audit team and responding to requests for documentation and information.
Works to a schedule as defined by the Quality Manager/Head of Quality. Conducts self-inspections/audits to ensure compliance with Quality Management System procedures and GMP regulations. Ensuring that a timely and effective communication and escalation of quality issues to the appropriate levels of management. Carries 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 and Training Technician in Glasgow employer: Curia
Contact Detail:
Curia Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality and Training Technician 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 resources to get comfortable discussing your experience and how it relates to the role.
✨Tip Number 3
Showcase your skills! Create a portfolio that highlights your QA projects, audits, and any continuous improvement initiatives you've been part of. This will give you an edge and demonstrate your hands-on experience.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who are proactive about their job search!
We think you need these skills to ace Quality and Training Technician in Glasgow
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Quality Assurance Specialist role. Highlight your 2+ years of QA experience and any specific GMP knowledge you have. We want to see how your skills match 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 background makes you a great fit for our team. Keep it concise but impactful!
Showcase Your Attention to Detail: In the QA world, attention to detail is key. When filling out your application, double-check for any typos or errors. We appreciate candidates who take the time to ensure their application is polished and professional.
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 to do!
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. Curia is looking for someone who can provide advice based on GMP and scientific rationale, so be prepared to discuss specific examples from your past experience where you've applied these principles.
✨Showcase Your Attention to Detail
In a role that requires reviewing deviations and complaints, demonstrating your attention to detail is crucial. Bring along examples of how you've successfully managed quality issues in the past, and be ready to explain your thought process and the steps you took to resolve them.
✨Prepare for Technical Questions
Expect technical questions related to Quality Assurance and regulatory commitments. Familiarise yourself with ICH and COSHH regulations, and think about how they apply to the role. Being able to articulate your understanding will show that you're not just experienced but also knowledgeable about the industry standards.
✨Communicate Effectively
Since this role involves working closely with a small team and communicating quality issues to management, practice articulating your thoughts clearly. You might want to prepare a few scenarios where effective communication made a difference in your previous roles, especially during audits or training sessions.