Skip to main content

Life Sciences

Commissioning, Qualification and Validation 

Commissioning, qualification and validation (CQV) is one of our biggest areas of business at Quanta. As a process primarily used within the biopharmaceutical & pharmaceutical industry, CQV ensures systems, facilities and equipment meet the design standards required for the end user. Because of its multi-faceted scope and the sheer industry demand for skilled workers, there is an abundance of interesting and rewarding opportunities on offer for contractors. We have been providing experienced CQV contractors since 2001, establishing ourselves as the go-to supplier for large-scale projects in the industry.

Commissioning and Validation

Our clients range in size and scale, including those commencing big-budget new build projects in locations throughout Europe and Asia. The varied locations of many of our CQV projects means we have built up an extensive international talent pool from which to source experienced candidates, often working flexibly to ensure we always meet the needs of those based in different time zones. Our project teams will also meet our clients on-site to ensure we fully understand their requirements, along with the benefits of working on the project – allowing us to communicate and attract the very best talent.

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: Permanent
Location

Hertfordshire

Description

Validation Specialist, Leading Biopharmaceutical Company, Oxfordfordshire Are you a Validation professional with experience in Process Validation? Are you looking to take the next step in your career

Options: Contract
Location

Limerick

Description

QA Validation Specialist, Global Pharmaceutical Company, Ireland Ireland is a hive of activity for the Life Sciences Sector at present with global players setting up new and expanding existing

Options: Contract
Location

Dublin

Description

Lab Validation Technician, New Large Scale Facility, Dublin Do you want to be part of one of the top 10 best companies to work for in Ireland? If so, this could be your chance! One of our global

Options: Contract
Location

County Tipperary

Description

Instrumentation Specialist - Global Pharmaceutical Company - County Tipperary - 11 month contract Our Partner in Tipperary area develops and supplies the active ingredients and final formulated

Options: Contract
Location

Dublin 16

Description

LIMS/ Lab System Specialist - Contract - Northern Ireland LIMS Specialist required for a world Leading bio tech organization who are at a Peak phase in establishing an innovative and industry

Options: Contract
Location

Brussels

Description

Senior CSV Specialist - Global Pharmaceutical Client – 7 Month Contract in Brussels, Belgium Our client, one of the worlds largest pharmaceutical organisations is responsible for developing and

Insights

International
mobilisation 

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