Role OverviewCritical Mass Consulting, LLC is seeking a Full Time CQV Engineer to join its San Diego field office. The role involves developing and executing commissioning/validation protocols, performing risk analyses, and supporting multiple client sites on validation projects.
What You Will Do
Develop and execute commissioning/validation protocols, perform risk analyses, support multiple client sites, and work on developing internal processes to increase quality of delivery and team engagement.
Why It Might Be a Fit
The ideal candidate will have a strong interest in Life Sciences, excellent written and verbal communication skills, and a minimum of 2 years of technical experience working in the pharmaceutical, medical device, or biotech industry.
Requirements
- Belief in our Core Values
- Strong interest in Life Sciences
- Excellent written and verbal communication skills
- Minimum 2 years of technical experience working in the pharmaceutical, medical device or biotech industry
- Strong understanding of Good Documentation Practices (GDP)
- Experience working in FDA regulated industries
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