Quality Engineer - CAPA

Quality Engineer CAPA

Onsite / hybrid Bakery Square PA (will move to Murrysville PA in the coming months)

12 Months

Job Description Summary

CAPA subject matter expert who can confidently advise and critically review Corrective and Preventive Actions (CAPAs) in various stages of the CAPA workflow and facilitate CAPA investigations from issue identification through implementation of solution and effectiveness monitoring.

Job Description

Your responsibilities

Critically review product and process Corrective and Preventive Actions (CAPAs) in various stages of the CAPA workflow

Facilitate CAPA investigations from issue identification through implementation of solution and effectiveness monitoring

Support updating the business processes relating to CAPA

Responsible for performing timely detailed CAPA engineering tasks like assessing issue descriptions reviewing CAPA data sources assisting with root cause analysis and quality problem solving

Project manage all aspects of CAPA activity which includes gaining the commitment of cross functional resources scheduling CAPA team meetings and ensuring CAPA deliverables per project timelines

Support and prepare spokespersons in representing CAPAs during audits and CAPA Review Board meetings

Lead and mentor crossfunctional teams with the implementation of appropriate root cause analysis techniques

Analyze quality monitoring data sources and apply statistical techniques to identify existing and potential causes of nonconformances

Work effectively with all levels of management to ensure CAPA action plans can be supported and that costs / resources needed to implement the plan are available

Perform periodic trend analysis and corrective action effectiveness measures of all quality system events and identify opportunities for improvement

To succeed in this role you should have the following skills and experience

At least a bachelors degree in an engineering or scientificrelated field or other plus equivalent technical experience working in a medical device environment

At least 10 years practical experience with CAPA

Able to understand and analyze complex problems including software and hardware design issues

Demonstrated knowledge of tools and techniques required to perform thorough root cause analysis and develop strong investigations

Strong understanding of appropriate global regulations requirements and standards such as 21 CFR Parts 803 806 and 820 ISO 13485 ISO 9001 and ISO 14971Demonstrated ability to partner with the business and effectively interact with and influence employees and managers on all levels

Strong Project Management skills including ability to project manage all CAPA activities

Strong reasoning and logical thinking skills

Excellent written and verbal communication skills in English

Key Skills

APQP,Quality Assurance,Six Sigma,ISO 9001,PPAP,Minitab,Root cause Analysis,ISO 13485,Quality Systems,Quality Management,As9100,Manufacturing

Employment Type : Full Time

Experience : years

Vacancy : 1