CVQ EngineerOur client is a global biopharmaceutical company whose purpose is to innovate to transform the lives of patients and their families. Dedicated to developing life-changing medicines for people with serious diseases - often with limited or no therapeutic options our client has a diverse portfolio of marketed medicines and novel product candidates, from early- to late-stage development.This is a fixed term 6 month contract for immediate startThe key items to be qualified will be vessels, powder transfer systems (PTS), a parts washer, a liquid filling (bottling) machine and necessary updates to existing utilities.Brief Description:Reporting into the head of Manufacturing Sciences & Technology (MS&T), the role will ensure that systems and equipment are properly installed on the site, meet design specifications and are capable of producing high-quality product.This position may also support new process introduction and process qualification activities as required.The role may work in close collaboration with a project team lead who is the primary owner of the team processes, tools, metrics, and all aspects of project management to ensure successful completion of assigned projects.Essential Functions/ResponsibilitiesSupport the on-site Commissioning, Qualification and Validation (CQV) process. Draft, review, and approve CQV documentation (protocols, reports, change controls, deviations) as appropriate. Support re-qualification activities as required.Support the installation and startup of equipment and systems in a safe compliant manner. Verify that all equipment functions safely and meets user requirements. Ensure systems and equipment that impact product quality and patient safety are correctly installed and fit for intended use.Assessment of site systems for compliance with new or developing regulatory expectations as they apply to validation.Generate documentary evidence that processes and systems consistently produce reproducible results in compliance with regulatory standards.Support process validation / qualification activities as required.Support and lead continuous improvement activities.Provide trouble shooting & technical input to significant issues/ deviations etc.Work with global functions and other sites to facilitate transfer of technical knowledge.Support the global regulatory team in dossier development or post market changes as required.Provide support as appropriate to New Product and Technology Introduction teams.Support manufacturing and site activities with technical support as required.Required Knowledge, Skills, and AbilitiesMinimum 3 years pharmaceutical industry experience in Commissioning, Qualification and Validation processes.Experience supporting manufacturing, process support, process validation and process troubleshooting in a GMP environment desirable.Experience in drug product and packaging environments preferential.Excellent organizational, verbal, communication, presentation, and data analysis skills.Ability to work independently, as well as a member of multi-disciplinary teams in a dynamic, fast-paced environment.Ability to establish collaborative working relationships at all levels, regardless of seniority.Strong understanding of project management processes, risk management processes, pharmaceutical quality management systems and pharmaceutical regulations.High level of competence with MS Word/Excel/Power point.Experience of project management on technical programs is desirable.Ability to manage multiple assignments, changing priorities and achieve required deadlines.Required/Preferred Education and LicensesBSC in life sciences, engineering related field, or equivalent combination of education and work-related experience required.Cv to