Reference Number:
R36078
Nottingham (United Kingdom)
Full time
, Fixed Term
Quality
Senior QA Associate - GMP Manufacturing - Onsite
We are looking for a Senior QA Associate to join our team in Nottingham on a fixed term basis.
We are looking for a Senior QA Associate for the QA and EHS department at Sartorius Albumedix Limited. In this role, you will be responsible for reviewing and approving Batch Manufacturing Records, carrying out the Batch Release process, deviation review, internal and external supplier audits, as well as working closely with customers. You will be responsible for reviewing documentation related to manufacturing, including QC worksheets, and will also undertake administrative duties to ensure the organization meets high quality standards and compliance obligations.
The team consists of 5 professionals, and we are looking forward to shaping the future with you.
This position is available full–time on a fixed–term basis with a view to start in October 2025 until October 2026. It is an onsite role in central Nottingham and the site is easy to get to, being a short walk from the train station and tram stop.

ATTRACTIVE WORKING CONDITIONS:

• 35 hours working week
• 25 days annual leave, plus public holidays
• Free parking on site, easily accessible from the city centre and transport hubs
• Social Committee – with both free and subsidised social events
• Private Healthcare
• Pension Scheme
• Free onsite fitness classes
• Group Life Assurance
• Group Income Protection
• Free annual flu vaccinations
• Employee Assistance Programme for colleagues and their families
• One day per year given to be a ‘Helping Heart’ within your local community
  Ready to join Sartorius?
  About Sartorius
  Sartorius is part of the solution in the fight against cancer, dementia, and many other diseases. Our technologies help translate scientific discoveries into real-world medicine faster, so that new therapeutics can reach patients worldwide.
  We look for ambitious team players and creative minds, who want to contribute to this goal and advance their careers in a dynamic global environment. Join our global team and become part of the solution. We are looking forward to receiving your application.

• On a daily basis you will undertake shared QA activities including, but not limited to, BMR (batch manufacturing records) and QC worksheets review, batch release, deviation and change control management whilst following SOPs and GMP regulations
• Support customer and internal audits, supplier evaluation, and product quality reviews
• Use of the electronic Quality Management System (eQMS - Dot Compliance) for administrative activities, including document issue and management of colleague training, and provide support in further implementation activities for the system
• Carry out training in QA processes and procedures
• You will work closely with other departments e.g. Manufacturing Operations, QC, Engineering, and Technology Group