Senior CQV Validation Project Lead

CAI; New Jersey; On-site; USD 120,000 - 180,000; Full time

Benefits offered by this job

4% retirement contribution

24 days PTO

5 sick days per year

Health insurance

Education support

70% long term disability paid by the公司

Job summary

CAI is seeking a Project Manager with strong CQV strategy and field execution experience. The ideal candidate will manage projects valued at $1M+ and lead teams of 6-8 engineers and consultants on defined scopes of work.

We value culture fit and proven ability to handle scope, schedule, and budgets. Requirements include a BS in science/engineering, 8–12 years in bio-pharma commissioning, and strong leadership, English communication, and risk-management skills.

Qualifications

• BS in a science or engineering field or equivalent experience
• 8-12 years’ Experience commissioning and qualifying bio-pharma systems equipment and systems
• Experience with risk assessments, qualification protocols, commissioning plans/test scripts and summary reports is desired
• Experience with CIP/SIP is desired
• Excellent skill in leading teams to perform complex tasks under pressure
• Excellent problem-solving skills
• Proficient and experienced with various Project Management software tools
• Customer-service focused
• Three (3) or more years serving as a program or project manager for life science projects with budgets of $1MM+.

Responsibilities

• Lead budget review meetings
• Lead daily huddle with your team
• Review a summary report
• Write a protocol
• Support your team executing in the field
• CAI project managers report to a client manager or an area manager

Skills

Team leadership

Problem solving

English communication

Customer service oriented

Project management familiarity

Education

BS in science or engineering field

Tools

Project Management software

Job description

CAI is seeking a Project Manager with strong CQV strategy and field execution experience. The ideal candidate will manage projects valued at $1M+ and lead teams of 6-8 engineers and consultants on defined scopes of work.

We value culture fit and proven ability to handle scope, schedule, and budgets. Requirements include a BS in science/engineering, 8–12 years in bio-pharma commissioning, and strong leadership, English communication, and risk-management skills.