At a Glance
- Tasks: Ensure quality compliance in drug manufacturing and support the QA team with technical expertise.
- Company: Curia, a global leader in drug development and manufacturing solutions.
- Benefits: Great perks including private healthcare, gym membership, and generous pension contributions.
- Other info: Flexible hours and a focus on employee engagement for career growth.
- Why this job: Join a dynamic team and make a real difference in pharmaceutical quality assurance.
- Qualifications: 2+ years of QA experience in GMP environments and a science-related qualification.
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.
In this role, you will assume responsibility for identifying corrections necessary to batch records or other QMS documents and for working closely with operational and laboratory functions to make suggestions to further enhance GMP compliance. 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.
Key Job Responsibilities include:
- Documents and reports of all work in adherence with GMP and departmental procedures.
- Performs batch review within the designated timelines described in departmental KPI.
- Authors and reviews SOPs.
- Reviews Type 1 change controls, and green category deviations.
- Provides feedback / corrections to authors and escalates concerns to the Quality Manager/Head of Quality where necessary.
- Raise CA/PA, approve “other” category CA/PA and review for completion “other” category CA/PA and support the completion of actions through liaison with other departments.
- Represent Quality Assurance in continuous improvement projects ensuring that change is performed in accordance with GMP, site procedures and industry regulations and guidelines.
- Identifies and performs personal development in line with agreed and documented annual goals.
- 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.
- Any other task deemed appropriate by line management.
- Ensuring that a timely and effective communication and escalation of quality issues to the appropriate levels of management.
- Carries out site internal audits and identifies areas of GMP improvement during their daily duties.
- Carries out training for QMS activities as defined by line management.
Qualifications
This role involves a high throughput of documents and information to process. 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.
- Have excellent communication skills, ensuring high levels of documentation; legible writing; clear structure.
- You must already hold the right to work in the UK as we are unfortunately unable to offer sponsorship.
Excellent Benefits, with a big focus on employee engagement. Up to 9% employer contribution to pension, Dental, Private healthcare, 4x salary life scheme, gym membership contribution, cycle to work, holiday purchase scheme, sick pay, and more. Hours - 37.5 (flexible start/finish times).
Quality Assurance Specialist employer: Curia
Curia Glasgow is an exceptional employer that prioritises employee engagement and development, offering a comprehensive benefits package including up to 9% employer pension contributions, private healthcare, and flexible working hours. Our collaborative work culture fosters continuous improvement and personal growth, making it an ideal environment for Quality Assurance Specialists looking to make a meaningful impact in the pharmaceutical industry.
StudySmarter Expert Advice🤫
We think this is how you could land Quality Assurance Specialist
✨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 creating a list of common interview questions and practising your responses. This will help you feel more confident and ready to impress!
✨Tip Number 3
Showcase your experience! When you get the chance to chat with potential employers, highlight your previous QA roles and how you've contributed to compliance and improvements. Use specific examples to demonstrate your skills and dedication.
✨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 and engaged with our company. So, go ahead and submit your application today!
We think you need these skills to ace Quality Assurance Specialist
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 perfect fit for our team. Keep it concise but impactful!
Showcase Attention to Detail:Since this role requires a keen eye for detail, make sure your application is free from typos and errors. We appreciate clarity and precision, so present your information in a well-structured manner.
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 shows you’re serious about joining our team!
How to prepare for a job interview at Curia
✨Know Your GMP Inside Out
Make sure you brush up on your knowledge of Good Manufacturing Practices (GMP) before the interview. Be ready to discuss how you've applied these principles in your previous roles, especially in relation to batch records and quality management systems.
✨Showcase Your Attention to Detail
As a Quality Assurance Specialist, attention to detail is crucial. Prepare examples from your past experience where your meticulous nature helped identify issues or improve processes. This will demonstrate your fit for the role and your commitment to quality.
✨Prepare for Technical Questions
Expect technical questions related to quality assurance processes, deviation management, and regulatory compliance. Review common scenarios you might face in the role and think about how you would handle them. This will show that you're not just knowledgeable but also practical.
✨Communicate Clearly and Confidently
Since excellent communication skills are essential, practice articulating your thoughts clearly. Whether discussing your experience or answering questions, ensure you convey your ideas in a structured manner. This will help you stand out as a strong candidate.