QA Specialist NDP

## QA Specialist NDPApplylocations:
Wrexhamtime type:
Full time posted on:
Posted Todaytime left to apply:
End Date:
June 19, 2026 (21 days left to apply) job requisition :
R-21497
*
* Title:

** QA Specialist NDP
** Company:
** Ipsen Biopharm Ltd
** About Ipsen:
** Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas:
Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K, we tackle areas of high unmet medical need through research and innovation. Our passionate teams in more than 40 countries are focused on what matters and endeavor every day to bring medicines to patients in 88 countries.

We build a workplace that champions human-centric leadership and fosters a culture of collaboration, excellence and impact. At Ipsen, every individual is empowered to be their true selves, grow and thrive alongside the company’s success. Join us on our journey towards sustainable growth, creating real impact on patients and society!

For more information, visit us at
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*
* Job Description:

**** 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 excellence.### ###
** In 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…