Apsida Life Science have partnered with a leading biotech and research company to present the following role:
Company Overview
This clinical-stage biopharmaceutical company develops precision small-molecule therapies targeting key immune signaling pathways for neurological and immune-mediated diseases. Its pipeline includes oral and topical candidates for neuroinflammatory and dermatologic conditions, with lead programs in early clinical development and supported by strong venture backing.
Job Title- Quality Assurance Consultant (GCP)
• Location: UK
• Type- Remote
• Duration- 12 months
Key Responsibilities
* Provide QA oversight for Phase 2 clinical trials, ensuring full compliance with GCP requirements and applicable SOPs.
* Conduct and support GCP audits (internal, vendor, and investigator site audits) and manage CAPAs to closure.
* Ensure clinical activities comply with FDA and MHRA regulatory expectations, supporting inspections and regulatory interactions.
* Advise biotech project teams on quality systems, risk management, and compliance throughout the clinical development lifecycle.
* Review and approve clinical trial documentation to ensure accuracy, consistency, and regulatory readiness.
Requirements
* GCP experience
* Relevant Life Science degree
* Minimum of 5 years experience
* Own Limited Company (preferred)
* Biotech industry experience
* FDA/MHRA regulatory experience
* Phase 2 clinical trial experience
* Auditing
If you are interested in learning more, please reach out to Mufaro Mpofu:
mufaro.mpofu@apsida.com
www.apsida.co.uk
Apsida Life Science is a specialist recruitment business based in London (UK), Redhill (UK), Boston (USA) & Pretoria (South Africa) that is dedicated to delivering the best talent to the Life Science industry. We believe there is a gap in the market for a cost effective, high quality and trusted recruitment service that puts the candidate journey at the heart of the recruitment process.