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.
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
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
