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For Companies At a Glance
- Tasks: Manage quality assurance processes and support audits in a biopharmaceutical environment.
- Company: Join a successful biopharmaceutical CRO in Livingston with a supportive culture.
- Benefits: Enhanced annual leave, free parking, and global career progression opportunities.
- Why this job: Make a real impact in quality assurance while advancing your career in a dynamic industry.
- Qualifications: 12 months experience in a GMP/GLP lab and strong attention to detail.
- Other info: Flexible working hours and recognition for achievements.
The predicted salary is between 36000 - 60000 £ per year.
Overview
Location: Livingston, Scotland
Hours: 39 hours/week, Monday–Friday (flexible start/end times available)
Contract Type: Permanent, Full-Time
Visa Sponsorship: Not available
Seeking an accomplished GMP QA professional to join a successful biopharmaceutical CRO in Livingston.
Role
Job Title: Quality Assurance Specialist
Responsibilities
- Administration and development of LIMS and other IT systems
- Review and approval of procedures, protocols, reports, and certificates of analysis
- Management of quality KPIs and metrics
- Support for internal audits, client audits, and regulatory inspections
- Coordination of quality documentation and controlled substances processes
- Delivery of QMS and eLIMS training to staff
- Lead or support continuous improvement initiatives in the QMS
- Deputising for QA Management where required
Qualifications
- Minimum of 12 months working within a GMP/GLP regulated laboratory
- Experience within quality assurance would be a distinct advantage
- Exemplary attention to detail and ability to liaise across multiple departments and externally
Benefits
- Enhanced Annual Leave (including sell-back options and service-linked increases)
- Free On-site Parking
- Enhanced Maternity, Adoption & Paternity Schemes
- Global career progression opportunities
- Access to Employee Assistance and Health & Wellbeing Programmes
- Recognition for service, special achievements, and life events
Details
- Seniority level: Associate
- Employment type: Full-time
- Job function: Quality Assurance
- Industries: Pharmaceutical Manufacturing
Interested? Apply now to take the next step in your Quality Assurance career within a supportive and forward-thinking organisation.
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GMP QA Specialist employer: VRS Recruitment
Contact Detail:
VRS Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land GMP QA Specialist
✨Tip Number 1
Network like a pro! Reach out to your connections in the biopharmaceutical industry, especially those who work in GMP QA. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of quality assurance processes and regulations. We recommend practising common interview questions related to GMP and GLP to show you're the right fit for the role.
✨Tip Number 3
Don’t forget to showcase your attention to detail! During interviews, share specific examples of how you've managed quality KPIs or supported audits. This will help you stand out as a candidate who truly understands the importance of quality in the biopharmaceutical sector.
✨Tip Number 4
Apply through our website for the best chance at landing that GMP QA Specialist role. We make it easy for you to submit your application and keep track of your progress, so don’t miss out!
We think you need these skills to ace GMP QA Specialist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your GMP/GLP experience and any relevant quality assurance roles. We want to see how your skills match the job description, so don’t be shy about showcasing your achievements!
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 you can contribute to our team. Keep it concise but engaging – 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 best selves, so double-check everything before hitting send!
Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates from our team!
How to prepare for a job interview at VRS Recruitment
✨Know Your GMP Inside Out
Make sure you brush up on your Good Manufacturing Practice (GMP) knowledge. Be ready to discuss specific regulations and how they apply to quality assurance in a biopharmaceutical setting. This shows you’re not just familiar with the terms, but you understand their practical implications.
✨Showcase Your Attention to Detail
As a GMP QA Specialist, attention to detail is crucial. Prepare examples from your past experience where your meticulous nature made a difference. Whether it was catching an error in a report or improving a procedure, these stories will highlight your strengths.
✨Familiarise Yourself with LIMS and QMS
Since the role involves administration of LIMS and QMS, make sure you know the basics of these systems. If you’ve used similar software before, be ready to explain how that experience translates to this role. It’ll show you’re proactive and tech-savvy.
✨Prepare for Scenario-Based Questions
Expect questions that ask how you would handle specific situations, like an internal audit or a regulatory inspection. Think through potential scenarios and how you would approach them, demonstrating your problem-solving skills and ability to work under pressure.
