Job Description
SciPro is collaborating with one of our long-standing pharmaceutical partners to support on a new search within the UK. We are searching for an organised administrator with excellent attention to detail and an interest in pharmacovigilance and regulatory affairs, to join the Clinical & Regulatory Affairs team of a well-established healthcare organisation.
In this role, you will provide essential administrative support across pharmacovigilance and medical device regulatory activities, ensuring customer safety and product quality information is accurately recorded, managed, and communicated. You'll work closely with a range of internal teams and external partners, supporting compliance with regulatory requirements and contributing to patient safety.
Key responsibilities include:
Managing customer safety and product quality reports, ensuring timely documentation and follow-up.
Maintaining pharmacovigilance and regulatory databases and controlled documents.
...
In this role, you will provide essential administrative support across pharmacovigilance and medical device regulatory activities, ensuring customer safety and product quality information is accurately recorded, managed, and communicated. You'll work closely with a range of internal teams and external partners, supporting compliance with regulatory requirements and contributing to patient safety.
Key responsibilities include:
Managing customer safety and product quality reports, ensuring timely documentation and follow-up.
Maintaining pharmacovigilance and regulatory databases and controlled documents.
...
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Submit ApplicationJob Details
- Location Hitchin, Hertfordshire
- Job Type Full-time
- Category other-general
- Posted Date July 03, 2026
- Application Deadline August 12, 2026