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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

London

Description

Brilliant Opportunity in central London to support a rapidly growing Gene Therapy company with their transition into commercial manufacturing. They are looking for a Validation Officer to support

Options: Permanent
Location

Oxfordshire

Description

Validation Specialist , Up to £50k, Oxfordshire Are you a Validation professional with experience in Process Validation? Are you looking to take the next step in your career and be part of an

Options: Contract
Location

Cork

Description

CQ Engineer – 12 months – Contract – ASAP - Cork, Ireland I am currently working with a Leading Global Pharmaceutical client based in the beautiful Cork, Ireland. Due to a large volume

Options: Contract
Location

Dublin

Description

Equipment Engineer – Global Pharmaceutical Company – Capital Project – Dublin – long term contract Do you want to be part of one of the top 10 best companies to work for in Ireland? If

Options: Permanent
Location

Cork airport

Description

Validation Specialist, Up to £50k, Oxfordshire Are you a Validation professional with experience in Process Validation? Are you looking to take the next step in your career and be part of an

Options: Contract
Location

Wiltshire

Description

Global Pharmaceutical Organisation require a Validation Engineer to support on a CAPEX Investment Project.  We have an excellent contract opportunity for an experienced validation engineer to work

Insights

International
mobilisation 

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