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Life Sciences Technical Consultant - Los Angeles

Critical Mass Consulting
Los Angeles, CA

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Job Details

Full-time

Qualifications

Good documentation practices (GDP)
GMP
Pharmaceutical company experience
Technical writing experience within technology
FDA regulations

Full 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:

Project Management
Process Engineering
Quality Management Systems Development
Validation Program Development
GMP System Commissioning and Qualification
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.

Develop and perform Risk Analyses
Support multiple client sites on validation projects throughout the Los Angeles area
Work on developing internal processes to increase quality of delivery, and increase team engagement
Consult clients on latest industry approaches to commissioning, qualification and validation
Develop standards and best practices for development and validation activities
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

Establish or maintain quality systems, including Change Control, Deviations, and CAPAs programs
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.
- People Come First
- We Build Together
- Empowering Growth and Leading People to Make a Difference
- Joy and Discipline, Life in Balance
Strong interest in Life Sciences and a passion for helping others
Excellent written and verbal communication skills, emphasizing strong technical writing skills
Minimum 2 years of experience working in the pharmaceutical, medical device or biotech industry
Strong understanding of Good Documentation Practices (GDP), and experience working in FDA regulated industries
Proficiency in no-code business intelligence tools is a nice to have (Power BI, Tableau, Looker, etc.)

Quick Apply

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Critical Mass jobs

Life Sciences Technical Consultant - Los Angeles

Full Time CQV Engineer – San Diego

Director of Sales, Walmart

Director of Sales, Publix

Director of Sales, Kroger

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