Life Sciences
Regulatory Affairs jobs.
Regulatory affairs teams keep products licensed and compliant across MHRA, EMA and FDA routes, and post-Brexit dual submissions have kept demand high. Actionus supplies regulatory officers, managers and consultants for contract and permanent roles in pharma, biotech and medical devices.
Specialities
What we recruit within regulatory affairs.
- Submissions and dossiers
- Labelling
- Medical devices (MDR)
- CMC
- Post-market surveillance
Where these roles sit
- —Pharmaceutical manufacturers
- —Medical device companies
- —Biotech scale-ups
- —Regulatory consultancies
Compliance you will need
- —Right to work, ID and verified employment history
- —Degree and professional qualification verification where the role requires it
- —GxP experience evidence (GMP, GLP, GCP) as relevant to the role
- —DBS where the work touches patient samples or clinical sites
- —Site specific induction, health surveillance and safety training
By location
Regulatory Affairs jobs near you.
Other life sciences professions