Supply Teachers

Prysmian Group; United Kingdom; On-site; GBP 40,000 - 60,000; Full time

Job summary

A healthcare company in the United Kingdom seeks a Qualified Person to ensure product quality and compliance within its dynamic Wrexham site. The successful candidate will certify finished product batches, lead quality initiatives, and provide expert advice on regulations. Candidates should have experience in sterile pharmaceutical manufacturing and be solution-oriented communicators. Join a collaborative team dedicated to innovation and patient safety in a supportive environment.

Qualifications

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

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.

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. If you are passionate about ensuring medicines are safe and meet the highest standards, join us as a Qualified Person and play a critical role in protecting patients by guaranteeing product quality and compliance.

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.

Requirements

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

Why Join Us? You'll be part of a collaborative team committed to excellence, innovation, and patient safety. We offer a supportive environment where your expertise truly matters. Apply now and help us deliver medicines that make a difference!