EV Process Auditor

3 weeks ago


Danvers Massachusetts, United States ITW Performance Polymers Full time
Job Description

Our Quality team plays an important role in our business operations and success. As an EV Process Auditor, you will get to work in a fast-paced and dynamic environment, leveraging your entrepreneurial spirit, affinity for detail- and process-oriented work, and collaborative skills to create great Quality outcomes. This is an exciting opportunity to utilize your knowledge of ISO and IATF requirements to support the growth of an industry-leading Division within a Fortune 200 organization. Come grow with us 

ITW’S BUSINESS MODEL & CULTURE: 

We have an environment shaped by our decentralized, entrepreneurial culture that brings our exciting ideas to life.  Our people thrive in our “flexibility within the framework” approach. 

We are committed to providing you with growth and development opportunities that maximize your unique potential. 

Our culture empowers you to think and act like a business owner – we want your entrepreneurial spirit to thrive 

Be a part of One ITW/One Team, where everyone’s contribution matters in our quest to achieve our full potential. 

We live by our Core Values: 

We focus on the essential core of each business opportunity, fostering simplicity in how we think and execute.  

We gain strength through trial and error and work as a team through jointly sharing risk. 

We treat our customers and suppliers with integrity and transparency, and constantly strive to do the right thing. 

We deeply respect diversity at every level of the company and consequently promote an open environment where innovations can emerge from our various backgrounds and experiences. 

We trust our team members and are confident that they each work to the highest professional standards and in the company’s best interests. 

YOU MIGHT LIKE THIS JOB IF YOU… 

You enjoy creating and following structured processes and easily pick up on granular details others may miss. 

Are intrinsically motivated. You are self-driven, thrive in an autonomous environment, and are always proactively looking to make progress on your goals and tasks. 

Enjoy working with a team, but also thrive when you work independently. 

PRIMARY RESPONSIBILITIES: 

Conduct manufacturing process audits to verify, review and evaluate the manufacturing process and critical process monitors to established criteria. 

Perform manufacturing process audits to verify conformance to technical documentation, engineering specifications, and contractual requirements. 

Coordinate process audits of documented engineering procedures and report the results to management. 

Produce audit observation reports, defend audit findings and assist with corrective actions. 

Investigate issues, monitor and enter corrective actions as necessary, and manage Supplier Corrective Action Request (SCAR) programs.  

Perform Root-Cause-Analysis and Corrective/Preventive action planning, and present audit reports to senior level management with suggestions and feedback for corrective actions. 

Perform audits, maintain documentation, and ensure that company processes and procedures are compliant with ISO and IATF guidelines. 

Perform manufacturing system audits to ensure elements of the quality system have been developed, documented and effectively implemented. 

Develop audit checklists based on contracts, government requirements, and internal procedures to ensure compliance. 

Participate as an internal auditor for the Quality Management System. 

Audit all processes to verify compliance against product work instructions, raw material tolerances, product manufacturing parameters, internal packaging standards, finished goods FIFO and requirements dictated by internal procedures and ISO 9001 / IATF 16949 current revisions. 

Identify and develop process improvement plans/root cause analysis for Senior Management. 

Maintain documentation of completed audit findings, and pertinent notes in all tracking systems. 

Promote, support, and adhere to all safety, environmental, and quality-related policies and procedures in the facility. 

 


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