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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

Elstree

Description

A Pharmaceutical company born out of NHS are looking for a Production Team Leader to join their 24/7 manufacturing site working with blood plasma. We are looking for someone who is driven to succeed,

Options: Permanent
Location

Hertfordshire

Description

Do you relish the opportunity to work with a leading UK based Biologics manufacturer?  If yes, then this is the assignment for you! Our biotech client with manufacturing facilities just outside

Options: Contract
Location

United Kingdom

Description

Located in the South of England in commutable distance from Central London, this position would suit both local candidates and those wishing to commute from the city. Who are we looking for?

Options: Contract
Location

Republic of Ireland

Description

A fantastic opportunity to work in a state-of-the-art facility in Cork. You will be joining a leading Biopharma company who focus on a range of products which are life-changing for individuals. We

Options: Contract
Location

Tipperary

Description

Our Partner in the Tipperary area develops and supplies the active ingredients and final formulated product for a range of innovative medicines at its manufacturing and R&D facilities. The plant,

Options: Contract
Location

Dublin

Description

Long term contract assignment for an experienced Upstream Manufacturing Support Scientist. Joining a new state-of-the-art multi-product biologics manufacturing facility based in Dublin, we are

Insights

International
mobilisation 

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