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Quality Assurance Specialist 2

 

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 :

 

As a Quality Assurance Specialist II you will be responsible for leading and managing our supplier external audit program in the UK and supporting activities within the client services team such as hosting client audits and generating audit responses for our client audit program.  The successful candidate will be responsible for leading and coordinating the UK supplier schedule, conducting supplier audits, processing new vendors and reassessments and co-ordinating and processing supplier complaints. Key duties include documenting and reporting on supplier audit inspections, reviewing and approving new suppliers, supplier questionnaires, supplier quality agreements, and managing supplier complaints to ensure regulatory compliance. 

 

The successful candidate will also support the hosting of our customer audit program within the UK. Key duties will be hosting customer audits and coordinating audit activities (tours, document retrieval) with operations as well as co-ordinating audit responses and generating CAPAs related to customer audits.  The role will also involve overseeing company Quality Management System (QMS) documentation, including Event (Deviations and Out of Specifications), CAPA’s, Change Control, Effectiveness Checks and SOP’s. Your role will include travel within Scotland, UK & Europe to conduct client & supplier audits.

 

Who you are:

  • 2+ years’ experience in a quality role
  • Hold a Degree or equivalent in a Biological Science or Quality Management.
  • Previous experience working within a quality driven systems / or regulated environment (GMP and GLP).
  • Excellent attention to detail is essential as well as logical in thought
  • Strong Organisational skills
  • Presentation & interpersonal communication skills
  • Ability to set own work schedules to manage time and prioritise workload effectively.
  • Ability to train & develop functional skills in others and support colleagues cross functionally on operational and transactional tasks.


What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it 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 our diverse team!

 

Job Requisition ID:  280448
Location:  Glasgow
Career Level:  C - Professional (1-3 years)
Working time model:  Full-time

North America Disclosure
The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our Candidate Services team at 844-655-6466 from 8:00am to 5:30pm ET Monday through Friday. If you are a resident of a Connecticut or Colorado, you are eligible to receive additional information about the compensation and benefits, which we will provide upon request.  You may contact 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday, for assistance.

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Job Segment: QA, Quality Assurance, CAPA, Quality Manager, Technology, Quality, Management

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