IVDR Regulatory Assistant (Diagnostics) – Onsite Reading

Stirling Q&R; Reading; On-site; GBP 30,000 - 35,000; Full time

Job summary

Stirling Q&R in Reading is seeking a Regulatory Affairs Assistant to support an IVDR transformation project across the regulatory team. You will handle day-to-day regulatory queries and gather information for managers, enabling submissions without writing them yourself.

The role is a 12-month fixed-term contract, full-time and on-site in Reading. Start as soon as possible, ideally before Christmas, with a salary of £30,000–£35,000 per year.

Qualifications

• Ideally 1–2 years in regulatory affairs, quality or a related role in IVD, medical devices or life sciences.
• An interest in regulatory affairs and IVDR.
• Strong organisation, accuracy and written communication.
• A science degree or similar is helpful.

Responsibilities

• Answer customer facing regulatory queries accurately and on time
• Support the day to day running of the Regulatory Affairs function
• Gather, organise and prepare documents so the Regulatory Managers can compile technical files and submissions
• Support the IVDR transformation project with tracking, records and admin
• Work closely with Quality and other teams on site

Skills

Regulatory knowledge

Attention to detail

Written communication

Education

Science degree or related field

Job description

Stirling Q&R in Reading is seeking a Regulatory Affairs Assistant to support an IVDR transformation project across the regulatory team. You will handle day-to-day regulatory queries and gather information for managers, enabling submissions without writing them yourself.

The role is a 12-month fixed-term contract, full-time and on-site in Reading. Start as soon as possible, ideally before Christmas, with a salary of £30,000–£35,000 per year.