Qualified Person

RBW Consulting; Nottingham; On-site; GBP 50,000 - 70,000; Full time

Job summary

A leading pharmaceutical company in Nottingham seeks an experienced Qualified Person (QP) to support their growing UK operations. This hands-on role requires strong knowledge of GMP conditions and the ability to work flexibly across different hours and demands. You will be working with various teams while joining an organization with exciting development plans for the future. If this opportunity interests you, please reach out, even if the location isn't suitable, as there are other roles available.

Qualifications

• Eligibility to perform as a Qualified Person (QP) within the UK.
• Strong understanding and experience of GMP conditions.
• Flexibility regarding working hours and demands.

Responsibilities

• Join a growing UK operation with exciting development plans.
• Be hands-on and versatile in QP responsibilities.
• Collaborate with teams at all levels.

Skills

Eligibility to perform as a QP within the UK

Strong understanding of GMP aseptic and sterile manufacturing conditions

Flexibility in approach to working hours

Job description

Qualified Person (QP)

If you're an experienced QP, this is a fantastic opportunity to join a progressive pharmaceutical company in one of their core locations in the East Midlands.

Working with a market‑leading, global brand, you will join a growing UK operation that has exciting development plans set over the coming years. This role is a hands‑on QP position that will require versatility, flexibility and outstanding stakeholder skills, working with teams at all levels.

This will be a site‑based role on a 40‑hour week, Monday to Friday. However, given the expansion plans in manufacturing, flexibility around the working hours and days is critical.

For further information, please contact Mark Bux‑Ryan.

If this role sounds of interest, but the location is not right, please still get in contact as we have other similar positions live and pipelined for Q1 2026.

Key experience

• Eligibility to perform as a QP within the UK
• Strong understanding and experience of GMP aseptic and sterile manufacturing conditions, although non‑sterile manufacturing will be considered
• Flexibility in approach to working hours and demands of the role