In this role, you will be developing and executing CQV protocols using Good Documentation Practices (GDPs), investigating and resolving protocols exceptions or discrepancies, developing technical reports and CQV summary reports. You’ll also be responsible for reading and verifying field, facility and equipment drawings (e.g., P&IDs, AF&IDs, etc.), developing Standard Operating Procedures (SOPs), process workflows, and Construction Turnover Packages. We do have many client sites that we support and you will need to be flexible and willing to travel and work at various clients' locations, although this will account for less than 25% of your time. This role requires excellent organizational skills to manage deadlines and deliverables and exceptional communication skills (both written and verbal) as you will need to regularly communicate to internal stakeholders at various levels of our organization and external stakeholders such as clients and contractors.
- Bachelor’s degree in Mechanical, Chemical, or Electrical Engineering
- 0-2 years of experience in the Life Sciences industry
- Proficient with Microsoft Office – Word, Excel, PowerPoint, Project
- This position is based in-person and requires the successful candidate to live within a commutable distance.
- Flexibility and willingness to travel and work at various clients’ locations
