Manufacturing Quality Engineering Co-op

At Johnson & Johnson, we believe health is everything.

Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function:
Career Programs

Job Sub Function:
Non-LDP Intern/Co-Op

Job Category:
Career Program

All Job Posting Locations:
US345 MA Danvers - 22 Cherry Hill Dr

Job Description:

Johnson & Johnson is currently seeking a Manufacturing Quality Engineering Co-op to join our Manufacturing Quality Team located in Danvers, MA.

At Johnson & Johnson, we believe health is everything.

Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for humanity. Learn more at https://www.jnj.com/.

POSITION SUMMARY

The Manufacturing Quality Engineering Co-op will assist in sustaining and improving the quality processes across the manufacturing workflow to ensure quality product is produced and quality procedures are upheld.

KEY RESPONSIBILITIES


* Participate in the investigation of failures and formulation/implementation of action plans for non-conformances, internal corrective actions, and audit findings.


* Work in cross-functional teams to identify and address non-conformances throughout assembly to final shipment of product.

 


* Work with engineering teams to ensure quality procedures are followed in all manufacturing and distributing areas.


* Use Lean and Six Sigma tools to analyze non-conformance data and identify opportunities for improvement across Material Review Boards (MRB) and other processes. 


* Support and enforce company goals and objectives, policies and procedures, Good Manufacturing Practices, Good Documentation Practices, FDA QSR and ISO regulations.


* Assist in the development and maintenance of quality documentation, including investigation reports, correction efforts, CAPAs, and process FMEAs.


* Assist in reviewing process validations and equipment qualifications, including plans, protocols, and reports. 


* Utilize software tools to capture non-conformance data in order to analyze and identify trends for corrective actions or escalations.

REQUIREMENTS


* Undergraduate or graduate student pursuing a degree in engineering.

Focus on medical devices is preferred


* Ability to communicate...