Position : CQV Engineer Citizenship : Open to All Location : Various locations -- The location for their main office is in CT, but these will all be assignments that are at the end client's site, so the candidates must be willing to travel and should be used to that type of work. Duration : 12+ months Type : Contract Experience: 3 - 5 Years Office Base : Connecticut (assignments will be at various client sites) About the Role We're hiring experienced CQV Engineering Consultants to support major pharmaceutical and life sciences projects. This role involves leading validation lifecycle activities, collaborating cross-functionally, and delivering high-quality engineering documentation. You'll be embedded at client sites, driving execution from planning through final reports. Key Responsibilities Lead or support Commissioning, Qualification, and Validation (CQV) activities

Develop documentation: SOPs, requirement specs, protocols (IQ/OQ/PQ), and summary reports

Collaborate across teams to execute project deliverables on schedule

Mentor and train junior team members on project tasks and technical skillsets

Support succession planning through knowledge transfer and feedback

Engage with clients to identify needs and recommend project support solutions

Contribute to business development through networking and client relationship management

Core Project Areas Commissioning & Qualification (IQ/OQ/PQ)

Process Validation & Tech Transfers

GxP Computer Systems & Automation

Capital Projects & Facility Builds

Quality, Compliance & Regulatory Strategy

Due Diligence and Business Consulting

Must-Have Qualifications Bachelor's in Engineering, Life Sciences, or related (or equivalent military experience)

3+ years in CQV roles within pharma/life sciences

Experience writing and executing protocols, technical documentation

Strong leadership, coaching, and team development skills

Willingness to travel extensively for project work

Excellent communication and collaboration skills