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- Tasks: Drive quality and collaborate with teams to enhance our quality organisation.
- Company: Innovative company focused on healthcare, life science, and electronics.
- Benefits: Inclusive culture, growth opportunities, and a chance to make a real impact.
- Why this job: Join us to innovate and elevate humanity through science and technology.
- Qualifications: Bachelor’s degree in a relevant scientific area; travel may be required.
- Other info: Diverse team with a commitment to inclusion and personal development.
The predicted salary is between 36000 - 60000 £ per year.
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That’s why we are always looking for curious minds that see themselves imagining the unimaginable with us.
Your Role
In your role as Quality Specialist 1 within our flex team, you will drive quality and contribute directly to all quality teams within the quality organisation (Data audit, compliance, QC material management, document control and archive). You’ll work closely with quality team members across each quality department as well as internal stakeholders to make a real difference. This is your chance to bring your expertise, passion, and ideas to the table and help raise the bar in our quality organisation.
Key Responsibilities Include:
- Perform the review/approval of GxP documents, including protocols, technical specification (TS), batch records, workbooks, SOPs, validation protocols, and all other QMS documentation including highly custom and complex assignments.
- Perform data audit and approval of completed manufacturing or testing documentation as they comply with the stated regulatory standard and the approved TS, protocol or SOPs.
- Supports the Vendor Assurance program.
- Issuance and archiving of documentation.
- Supports material management program.
- Interacts with other departments to ensure compliance with internal procedures.
- Perform internal audits as required.
- QA review & closure of deviations, CAPA, GCC & EC.
- Support Stirling & Edinburgh sites as required, (Edinburgh less frequently).
Who You Are
Must have:
- Bachelor’s degree or above in a relevant scientific area.
- Ability to travel to Stirling & Edinburgh sites when required.
Nice To Have:
- Previous experience in one of the following areas: Document control, Archive, Vendor management, Data audits or Client audits.
- Experiences within GLP/GMP/GxP environment.
What we offer:
We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!
Quality Specialist 1 - Flex in Glasgow employer: Merck Life Science
Contact Detail:
Merck Life Science Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Specialist 1 - Flex in Glasgow
✨Tip Number 1
Network like a pro! Reach out to current employees on LinkedIn or at industry events. Ask them about their experiences and any tips they might have for landing a role with us.
✨Tip Number 2
Prepare for the interview by knowing our company inside out. Familiarise yourself with our products, values, and recent news. This shows you’re genuinely interested in working with us!
✨Tip Number 3
Practice your answers to common interview questions, but keep it natural. We want to see your personality shine through, so don’t be afraid to let your passion for quality and innovation show!
✨Tip Number 4
Apply directly through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re keen to join our team and work your magic with us!
We think you need these skills to ace Quality Specialist 1 - Flex in Glasgow
Some tips for your application 🫡
Show Your Passion: When writing your application, let your enthusiasm for the role shine through! We want to see how your passion for quality and science aligns with our mission to innovate and enrich lives.
Tailor Your CV: Make sure to customise your CV to highlight relevant experiences that match the job description. We love seeing how your background in document control or data audits can contribute to our quality organisation.
Be Clear and Concise: Keep your application straightforward and to the point. We appreciate clarity, so make sure your skills and experiences are easy to understand and directly related to the responsibilities of the Quality Specialist role.
Apply Through Our Website: Don’t forget to submit your application through our website! It’s the best way for us to receive your details and ensures you’re considered for this exciting opportunity to work with us.
How to prepare for a job interview at Merck Life Science
✨Know Your GxP Inside Out
Make sure you brush up on Good Practice (GxP) guidelines relevant to the role. Familiarise yourself with the specific documents you'll be reviewing, like protocols and SOPs. This will show your potential employer that you're not just a fit for the role, but that you’re genuinely passionate about quality standards.
✨Showcase Your Team Spirit
Since this role involves working closely with various quality teams and internal stakeholders, be prepared to discuss examples of how you've collaborated in the past. Highlight your ability to communicate effectively and work as part of a team to drive quality improvements.
✨Prepare for Scenario Questions
Expect questions that ask how you would handle specific situations, such as a deviation or a compliance issue. Think through your past experiences and be ready to explain your thought process and the steps you took to resolve similar challenges.
✨Ask Insightful Questions
At the end of the interview, don’t shy away from asking questions. Inquire about the company’s approach to quality management or how they support continuous improvement. This shows your interest in the role and helps you gauge if the company culture aligns with your values.