CQV Engineers / Specialists - Open Applications

VTI Life Sciences (VTI) is seeking forward-thinking and ambitious engineers looking to accelerate their careers in the pharmaceutical, biotechnology and medical device industries.

We offer an opportunity to help support our teams of industry subject matter experts and thought leaders while consulting with some of the biggest companies in the Life Sciences industries.

We are looking for multiple CQV Engineers with 5+ years of experience in Project Engineering and Validation for a long-term project to help  support Engineering and CQV activities related to the project expansion at our client's pharmaceutical facility in the Greater Los Angeles area.  Our client is seeking experienced validation Engineers / Specialists with a wide range of experience to fill the multiple roles.   RESPONSIBILITIES :

• Project Engineering Support User Requirement Specifications Functional Specifications Design Specifications SOPs Management of Change (MOC) Support FMEA activities.
• Support HAZOP processes.
• Perform Risk Assessments.
• Perform Gap Assessments.
• Project Closeout Documentation Turnover Package Generation Project Change Requests Support Client and A / E Firm in Project Design, Conceptual Design, Basic Design, Detailed Design and Design Review Construction Activities Generate and Manage Safety Management Plans and Documentation Disruptive Construction Activity Requests Job Hazard Analysis Lockout Tag Out Plan Hot Work Permitting Permit to Work Detour Plans Construction Signage Plant-wide Communications.
• Generate and Manage Quality Management Plans and Documentation Construction Control Plan Manage Installation, Operational, and Performance Qualification Summary Report Training and Documentation Risk Assessment and Mitigation Change Control Quality Audits Validation Support Equipment Installation Qualification, Operational Qualification and Performance Qualification Process Validation Equipment Cleaning Validation Facility Qualification Conduct validation of critical facility systems Software Validation   including data management and process control systems.

Compile Validation Reports Qualifications :