Pharmacovigilance / Regulatory
Pharmacovigilance (Drug Safety) and Regulatory Affairs are growing sectors for Quanta as governments become even more concerned with controlling the safety and efficacy of biopharmaceuticals, pharmaceuticals, medical devices and other products within life sciences; and the subsequent requirements that creates for our clients.
Both life science sub sectors rapid growth are due to ever-evolving drug product safety requirements, new technologies, changing customer requirements and relentless regulatory updates. People who work within these spaces are tasked with not only keeping up to date with, understanding and complying with the latest regulations, but also creating opportunities within the highly-regulated life sciences landscape. Because of this, skilled and qualified professionals are in hot demand by organisations across the UK, US, Europe and across Asia.
These resources cover a wide range of manufacturing areas, including (but not limited to):
- Primary biotechnology (upstream/downstream)
- Secondary (pharmaceutical and biotech)
- Formulation fill/finish
- Oral solid dosage
- Medical device
- Veterinary products
- Combination products
- Gene therapy