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Life Sciences

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.

Pharmacovigilance

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.

Manufacturing Areas

Manufacturing Areas

These resources cover a wide range of manufacturing areas, including (but not limited to):

  • Primary biotechnology (upstream/downstream)
  • API
  • Secondary (pharmaceutical and biotech)
  • Formulation fill/finish
  • Packaging
  • Oral solid dosage
  • Medical device
  • Nutraceuticals
  • Veterinary products
  • Combination products
  • Gene therapy

Latest Jobs

Options: Contract
Location

Tadworth

Description

Senior Process Engineer – Contract - Cork One of our global Pharmaceutical clients is looking for a Senior Process Engineer to join their team close to the picturesque and historical city of

Options: Permanent
Location

Copenhagen

Description

Pharmacovigilance Manager - Permanent - Denmark Are you looking for a new and exciting opportunity in Pharmacovigilance?  Would you be interested in working with a superb and energetic client?  

Options: Permanent
Location

Tadworth

Description

Senior Regulatory Affairs Executive - Permanent -Full time Do you want the opportunity to join one of the globe's largest pharmaceutical organisations?! Our client, one of the world’s largest

Options: Contract
Location

Buckinghamshire

Description

Regulator CTA Submission Manager - Contract 3 months - Buckinghamshire Are you looking for your next contract?  Are you searching for that exciting CTA opportunity? We have been appointed by our

Options: Permanent
Location

Paris

Description

Regulatory Medical Writer - Permanent - Full Time Are you looking for a new challenge?  Are you an experienced Regulatory Medical Writer seeking a new and exciting opportunity, if so read on. Our

Insights

International
mobilisation 

We are proud to offer first-class contract and permanent staffing solutions to clients on a global scale.