Qualified Person

Turner Townsend; Crewe; On-site; GBP 45,000 - 70,000; Full time

Job summary

A leading pharmaceutical company in the UK is seeking a Qualified Person to ensure product quality and compliance in a sterile manufacturing environment. You will certify and release finished product batches, ensuring adherence to UK and EU regulations. The ideal candidate will have experience in a similar role and the ability to propose innovative solutions. This role offers the chance to lead quality initiatives and make a significant impact in the pharmaceutical industry.

Qualifications

• Experience in a sterile pharmaceutical manufacturing operation is essential.
• Eligibility to act as a Qualified Person (QP) in the industry is required.
• Ability to propose innovative solutions and navigate ambiguity.

Responsibilities

• Certify and release finished product batches in line with UK/EU regulations.
• Ensure compliance with Good Manufacturing Practice (GMP) throughout production.
• Lead quality initiatives and continuous improvement projects.

Skills

Experience in a similar position

Solution-oriented mindset

Strong communication skills

Job description

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.

Join us as a Qualified Person and play a critical role in protecting patients by guaranteeing product quality and compliance. This is your chance to lead with purpose and make a real impact in the pharmaceutical industry.

Key Responsibilities

• Certify and release finished product batches in line with UK/EU regulations.
• Ensure compliance with Good Manufacturing Practice (GMP) throughout production.
• Lead quality initiatives and continuous improvement projects across the site.
• Provide expert advice on regulatory submissions, audits, and inspections.
• Act as a mentor and guide for quality matters within the team.
• Escalate and resolve issues that could impact product quality or timelines.

A Qualified Person will certify and release medicinal products, ensuring compliance with regulations and providing quality leadership.

Qualifications

• Experience in a similar position from a sterile pharmaceutical manufacturing operation.
• Eligible to act as a QP in the pharmaceutical industry.
• Solution‑oriented: able to propose innovative solutions and deal with ambiguity.
• Strong communicator across all levels.