Quality Specialist 1 - Flex

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!