Outgoing Quality Engineer Associate Jobs in California

May participate and/or perform vendor audits and qualifications. Participate in supplier approval and management activities.

Supplier Management/Production & Process Controls

Preferred: ASQ Certification, Lead Auditor Certification, ISO 13485 and/or FDA-regulated experience.

Maintain product quality by enforcing quality assurance policies and procedures and government requirements; collaborating with suppliers and operations when appropriate.

Resolve non-conformities and manage related CAPA activities.

2-5 years relevent work experience in a regulated industry

B.S. in Engineering/Chemistry/Biology/Technical or Science Discipline or equivalent combination of certification and work experience

Reviews procedural deviations for compliance to internal quality and external regulatory requirements

Computer skills – proficient in Microsoft Office, statistical software programs, operating systems, voice and email, etc.

Knowledge of quality systems and regulations for medical device industry

1-2 years of industry experience in medical device or equivalent s

Supports departmental activities in reducing product rejection, scrap and variances, and improving both the quality and business systems inefficiencies