Base: $160k - $230k; bonus/equity: not specified; ...
15+ years life science operational experience
10+ years validation and project management
Cgmp and fda validation methods expertise
This role involves leading a Regulatory Compliance Validation team for pharmaceutical, biotech, and medical device manufacturing projects within the Southern California area
Job Summary
This role involves leading a Regulatory Compliance Validation team for pharmaceutical, biotech, and medical device manufacturing projects within the Southern California area.
The successful candidate will leverage past professional experiences to expand Design Group's presence in the Life Science market sector while managing complex capital projects.
Design Group offers a supportive culture with professional development resources including mentorships, Individual Development Plans, and career path tools.
Matching Summary
This role involves leading a Regulatory Compliance Validation team for pharmaceutical, biotech, and medical device manufacturing projects within the Southern California area.
Salary
Base: $160k - $230k; Bonus/Equity: Not specified; Benefits: Not specified
Skills & Requirements
Must-have
15+ years Life Science operational experience
10+ years validation and project management
cGMP and FDA validation methods expertise
Clean utilities and bioprocess systems knowledge
Proposal creation and business development skills
Nice-to-have
Client side consulting experience preferred
Entrepreneurial spirit and leadership qualities
Experience with GAMP methodologies
Strong presentation and communication skills
Willingness to travel for client meetings
Key Requirements
BS Degree in Engineering or related technical degree
15+ years of Life Science operational & engineering experience
10+ years' experience in validation/quality service and project management
Demonstrated client development experience
Project Management experience in scope, cost, schedule, quality and risk