Job Details:
My client is a highly respected Consulting engineering firm that specializes in the pharm and biomedical market. They are seeking a Senior Validations Engineer with CQV and the ability to be a Project Lead. Responsibilities include:
- Min of 10yrs experience
- Full-time employment w/ benefits or 1099 contract arrangement
- Engineering / technical background required.
- Project lead role that can oversee other CQV engineers (when required), coordinate their work on a daily basis.
- Potential to work on and oversee multiple projects.
- Coordinate schedules, deliverables and track budgets.
- Must be self-motivated, a go-getter, resourceful, organized
- A “take-charge” personality is needed to push a project along.
- Must be able to develop test protocols utilizing client standards, vendor and design documentation. Be able to develop test scripts (not just handed a template to re-use).
- Wear multiple hats to function as a project lead and execute projects on their own.
- Coordinate with other CQV engineers as needed to support project execution (doc development/execution/reports)
- Experience in some or all of these areas:
- HVAC / BAS
- Clean Utilities
- Filling Machines
- Isolators
- CIP Systems
- Tanks & Transfer Systems
- Process Controls
- Proficient with MS Office suite of programs (Word, Excel at a minimum)
- Strong communication skills
- Plan to be onsite 4-5 days a week
- Job tasks may entail (at a minimum but not limited to)
- Project management tasks
- Scheduling
- Coordinate with Owner to complete the CQV process
- Oversee and draft Commissioning and IOPQ protocols
- Perform CQV execution as required
- Coordinate other CQV engineers to execute project work as needed
- Track and resolve issues with the owner
- Develop summary reports
Send a resume to dg@libertyjobs.com and/or call Dan Gallagher at 484 567 2084 for immediate consideration!
#midsenior
#Libertyjobs
#ConsultingEngineering
#CIVILMEP
#Validations
#Pharmacueutical
#CQV