Quality Engineer

Quality Engineer Katalyst Healthcares & Life Sciences - 4.0 Irvine, CA Job Details Contract 6 hours ago Qualifications Statistics Microsoft Outlook Six Sigma Green Belt Pharmaceutical regulatory compliance Process design Six Sigma methodology implementation Good documentation practices (GDP) GMP Mid-level GD&T Project management in manufacturing Post-sales issue resolution Technical support ASQC Certification Minitab Collaboration with product development teams Analysis skills Policy & process development Bachelor's degree in engineering Production validation processes Quality risk management Compliance documentation Design engineering Collaboration with manufacturing teams Engineering product development Design controls Biomedical regulatory compliance Quality audits Engineering functional testing Quality assurance within manufacturing

Full Job Description Summary :

New Product Development project or legacy product engaged in the development or sustenance of Pharmaceutical Electrophysiology medical device products. Performs ongoing execution of and provides guidance to good manufacturing practices, compliance to internal and external policies and other applicable standards. Roles & responsibilities : Provides product team support for multitude of new product development activities (e.g. engineering testing, design and process characterization, and other V&V activities) Assists in conducting Quality Assurance documentation reviews and audits as needed Support execution of risk management activities Support development and execution of relevant process development and validation activities (e.g.

IQ/OQ/TMV/APQ

) Utilizes multifaceted industry and process excellence standards in daily quality operations, including, but not limited to, good manufacturing practices (GMP) and Good Documentation Practices (GDP) Assists in addressing product or process issues (internally or externally manufactured) or in investigating customer complaints as needed Supports handling complex technical issues for manufacturing processes that are to be transferred to satellite facilities. Collaborate with cross-functional teams to achieve project team goals and objectives

Education & Experience:

A minimum of a bachelor's degree required (preferably in Engineering or related technical field); or a minimum of 2 years of quality, manufacturing, or research and development experience in a medical device or other regulated industry Ability to develop and implement Quality standards Thorough knowledge of Quality systems and processes, including GMP and QSR requirements for medical devices Knowledge of new product development design controls, and verification and validation (V&V) tools and methodologies Demonstrated problem solving skills Competent in using basic documentation applications such as MS Office (Word, Excel, Powerpoint, Outlook), Adobe PDF, etc. Ability to multi-task and manage multiple assignments in a timely manner Good verbal and written communication skills Strong analytical skills Ability to apply project management skills to ensure fulfillment of new product development requirements Experience working in both an FDA and European regulatory environment Expertise in NPD (New Product Development) process and Design/Process Validation American Society for Quality (ASQ) certification, Six Sigma experience, and/or knowledge of Process Excellence tools Six Sigma Green/Black Belt Certified Knowledge of GD&T (Geometric Dimensioning and Tolerancing) Knowledge of statistical analysis tools such as Minitab is a plus