QA Specialist NDP

Join Our Award-Winning Team at Ipsen Wrexham At Ipsen, we are committed to improving the lives of patients, with a special focus on advancing neuroscience therapies. Our Wrexham site is a vital part of this mission, delivering cutting-edge solutions in a dynamic and collaborative environment. We are proud to be Great Place to Work certified and a Shingo Bronze Medallion holder, reflecting our commitment to excellence, innovation, and continuous improvement.

With a recent £24 million investment in the site and a further £86.4 million expansion underway, there has never been a more exciting time to join us. If you are passionate about making an impact and want to be part of a team that values growth, innovation, and excellence, then Ipsen could be where you thrive!

Role summary

As a QA Specialist – NDP, you will play a key role in supporting a brand-new pharmaceutical manufacturing facility, ensuring robust quality oversight, operational readiness, and compliance with GMP requirements. You will partner closely with cross-functional teams to enable successful facility qualification, commercialisation, and ongoing manufacturing  this role you will:

Provide Quality Assurance oversight for the development and implementation of processes and procedures for the new Building 7 facility, ensuring alignment with GMP and Ipsen standards.

Review and maintain key operational documentation (SOPs, batch records, logbooks) and support deviation investigations, CAPAs, change controls, and OOS events.

Perform batch record review and provide real-time QA oversight during manufacturing activities to ensure compliant and timely batch release.

Act as a technical QA expert, supporting troubleshooting, resolving complex issues, and contributing to site projects and regulatory inspections readiness.

Deliver training and guidance on quality standards, procedures, and documentation to site teams, enabling a smooth transition to routine operations.

Drive continuous improvement by analysing quality metrics, identifying opportunities, and promoting a proactive quality culture across the site.

Requirements:

Significant QA experience within the pharmaceutical or biopharmaceutical industry

Strong knowledge of GMP, validation principles, and regulatory expectations

Experience in batch record review and supporting batch release activities

Excellent communication, problem-solving, and organisational skills

Ability to work both independently and collaboratively in a fast-paced, evolving environment

Degree, diploma or equivalent in a scientific discipline

Preferred:

Extensive QA experience, particularly within sterile or aseptic manufacturing environments

Knowledge of EU GMP Annex 1 and contamination control strategies

Experience supporting new facility start-up, expansion, or technology transfer projects

Familiarity with cleanroom environments (Grade A/B), aseptic techniques, and gowning practices

Experience with quality systems such as SAP, Blue Mountain, or electronic QMS platforms

Understanding and application of ICH Q9 Quality Risk Management principles

We are committed to creating a workplace where everyone feels heard, valued, and supported; where we embrace “The Real Us”. The value we place on different perspectives and experiences drives our commitment to inclusion and equal opportunities. When we include diverse ways of thinking, we make more thoughtful decisions and discover more innovative solutions. Together we strive to better understand the communities we serve.

This means we also want to help you perform at your best when applying for a role with us. If you require any adjustments or support during the application process, please let the recruitment team know. This information will be handled with care and will not affect the outcome of your application.
#J-18808-Ljbffr