Regulatory Affairs Consultant

JR United Kingdom; City Of London; Remote; GBP 100,000 - 125,000; Part time

Job summary

A pioneering biotech firm in London is looking for an experienced Regulatory Affairs Consultant to drive the regulatory strategy for biosimilar insulin products. The role is part-time and focuses on ensuring compliance with UK regulations while collaborating with CDMOs on biomanufacturing. Candidates should have significant experience in regulatory affairs within the biotech sector.

Qualifications

• Significant experience in regulatory affairs specific to biosimilars.
• Strong knowledge of CMC regulations and compliance.

Responsibilities

• Support regulatory strategy for biosimilar insulin products.
• Ensure compliance with UK regulations.
• Work with CDMOs to facilitate biomanufacturing.

Job description

Regulatory Affairs Consultant, London (City of London)

Location: London (City of London), United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views: 4

Posted: 14.08.2025

Expiry Date: 28.09.2025

Job Description:

Regulatory Affairs Consultant - CMC Strategy for Insulin Biosimilars (Part-Time / Contract)

Remote in UK | Contract | Biotech | Advanced Biomanufacturing

This biotech is pioneering the production of recombinant insulin. They are working with CDMOs to scale their biomanufacturing platform and are now seeking a highly experienced Regulatory Affairs CMC Consultant to support the regulatory strategy and ensure compliance for their biosimilar insulin products.