Staff Quality Engineer
Where
- Los Angeles, CA
What you'll be doing
- The staff quality engineer is responsible for ensuring product and process robustness and regulatory compliance through implementing and leading quality initiatives. This individual will be responsible for the execution and trending of quality metrics including corrective and preventative actions, non conformances, internal or external audits, annual drug product reviews, Change Control management and good documentation practices. The Staff Quality Engineer will be responsible for Quality Engineering support for base business, new product development, or supplier quality and ensure product and process robustness through quality initiatives. This individual will prioritize and implement improvement opportunities within the quality processes. This position will be a strong influence to ensure that all functions are trained in, understand, and comply with all relevant quality as well as providing guidance and collaborate with internal and external customers to ensure flawless execution of quality.
What your background should be
- 7 years of professional experience in quality assurance, specific to working within a GMP facility is required. Experience in conducting, executing and leading investigations is required. Experience in leading quality assurance projects is required. It is strongly preferred that this individual has quality assurance experience in pharmaceutical, cosmetics or personal care manufacturing environments. Experience in a production or process development environment in the consumer products or drug industry is preferred.
Required Schooling / Training
- Bachelor degree
Who is the client company
- The company is an American multinational medical devices, pharmaceutical and consumer packaged goods manufacturer.
- If you are interested in this position, send your resume to apply@kochdavis.com
