Life Sciences Technical Consultant - Los Angeles
Job Description
Job Description
Job Description: Life Sciences Technical Consultant – Los Angeles
Critical Mass Consulting, LLC is seeking individuals who want to learn and develop within a dynamic, start-up environment. We believe in our purpose: To develop a company which thrives on connectivity and engagement; to build a premier consulting organization, which rewards creativity, contribution, and growth.
Critical Mass Consulting, LLC is supporting Life Sciences clients in the areas of:
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Project Management
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Process Engineering
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Quality Management Systems Development
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Validation Program Development
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GMP System Commissioning and Qualification
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Cleaning and Process Validation
- Computerized System Validation (CSV)
Our company places an emphasis on continuous personal development. This includes support/financing of technical training, mentorship, and development of high performance teams.
Job Description:
Critical Mass Consulting, LLC is recruiting Consultants to join its Los Angeles, CA field area. If you have a passion for Life Sciences and helping others, we are interested in discussing our company, our process and what it means to join our team-focused organization.
Expected Activities
Develop and execute commissioning/validation protocols, such as factory and site acceptance test (FAT, SAT), installation, operational and performance qualifications (IQ/OQ/PQ) on various critical systems, process equipment and supporting processes.
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Develop and perform Risk Analyses
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Support multiple client sites on validation projects throughout the Los Angeles area
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Work on developing internal processes to increase quality of delivery, and increase team engagement
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Consult clients on latest industry approaches to commissioning, qualification and validation
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Develop standards and best practices for development and validation activities
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Manage medium-small teams and/or projects
Additional Responsibilities
Participate in team-based projects, supporting life sciences clients in the areas of Quality Systems and Validation
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Establish or maintain quality systems, including Change Control, Deviations, and CAPAs programs
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Consult clients on latest industry approaches to commissioning, qualification and validation
Required Qualifications:
- Belief in our Core Values. These 4 values provide the foundation for how we operate as a company. With these common shared values, we can effectively accomplish our mission of organizational excellence.
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People Come First
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We Build Together
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Empowering Growth and Leading People to Make a Difference
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Joy and Discipline, Life in Balance
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Strong interest in Life Sciences and a passion for helping others
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Excellent written and verbal communication skills, emphasizing strong technical writing skills
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Minimum 2 years of experience working in the pharmaceutical, medical device or biotech industry
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Strong understanding of Good Documentation Practices (GDP), and experience working in FDA regulated industries
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Proficiency in no-code business intelligence tools is a nice to have (Power BI, Tableau, Looker, etc.)
