CQV Engineer: Life Sciences Validation Specialist

Critical Mass Consulting, LLC; San Diego (CA); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Support for technical training

Mentorship

Development of high-performance teams

Job summary

A consulting firm in San Diego seeks a Full Time CQV Engineer passionate about Life Sciences. Successful candidates will develop and execute validation protocols, manage projects, and consult clients on industry best practices. Required qualifications include a strong interest in Life Sciences and at least 2 years of experience in regulated industries. The role emphasizes team collaboration and continuous personal development.

Qualifications

• Minimum 2 years of technical experience in pharmaceutical, medical device, or biotech industry.
• Experience in FDA regulated industries.

Responsibilities

• Develop and execute commissioning/validation protocols on critical systems.
• Support multiple client sites on validation projects.
• Manage medium-small teams and/or projects.

Skills

Strong interest in Life Sciences

Excellent communication skills

Strong technical writing skills

Understanding of Good Documentation Practices (GDP)

Job description

A consulting firm in San Diego seeks a Full Time CQV Engineer passionate about Life Sciences. Successful candidates will develop and execute validation protocols, manage projects, and consult clients on industry best practices. Required qualifications include a strong interest in Life Sciences and at least 2 years of experience in regulated industries. The role emphasizes team collaboration and continuous personal development.