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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: Contract
Location

County Limerick

Description

Fancy a change from busy city life? Why not consider working for a global Biotechnology organisation in the picturesque Munster region of Ireland!  An international airport just 30 minutes from

Options: Contract
Location

Paris

Description

I am currently recruiting for a C&Q Manager to work for our client based in the Paris area on their Cell and Gene Therapy project on an initial 12-month contract basis. Responsible for leading and

Options: Contract
Location

Wiltshire

Description

Cleaning Process Expert required to develop cleaning procedures for a global pharmaceutical organisation on an exciting CAPEX project introducing new technology to site.  This role is a contract

Options: Contract
Location

Dublin

Description

Bulk Drug Substance Manufacturing facility are in need of an experienced QA Validation Engineer  who has knowledge of both Upstream & Dowstream processing to execute the site QA activities from

Options: Contract
Location

Australia

Description

One of our clients, a global biopharmaceutical client is looking for a CSV Specialist to join their team on their site in Sydney, Australia on a long term contract. The successful candidate will be

Options: Contract
Location

Cheshire

Description

Quanta are looking for a CSV engineer with data integrity experience for a project in Cheshire. We're looking for someone who can combine this experience, plus reviewing for a serialisation project

Insights

International
mobilisation 

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