Jobs for People with MS: National MS Society

We are excited to be named one of the World’s Best Workplaces by Fortune Magazine!

We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.

Basic Function:

Manufacturing Quality Engineer role is to implement a unified approach to Quality in Stryker with the intent to deliver high quality products and services in a manner that meets the high standards held by Stryker.

Responsibilities:

This role will provide support to the Site Quality team to ensure compliance to technical, regulatory and Stryker requirements.

• Executing Change Managements & Manufacturing Changes associated with Machine moves, Process changes, validation updates.

• Executing Production part approval process for any change request.

• Good hands-on experience on Validation (Validation PSPs, EQ, MSA execution)

• NC/ CAPA for internal Manufacturing issues (Clean, Pack, Label, Gage)

• Driving Internal Continuous Improvement projects at Site.

• Executing Gage Evaluation from QT's & focus on Gage/ fixture Updates & Development.

• Reviewing & providing inputs on Supplier Material Certificates.

• Ownership for site quality performance and measurement including KPI’s and participate in supplier performance reviews.

• Support quality issues with site & partner with Internal Customers; Lead effective supplier containment and corrections/corrective action.

• Provide support to Internal/ External Customer groups on compliance issues related to assigned sites.

• Participate in cross- functional teams in the development of new products or changes related to current products in meeting customer requirements.

• Applies sound, systematic problem-solving methodologies (5Why, DMAIC, 8D, C&E) in identifying, prioritizing, communicating, and resolving quality issues - NC & CAPA.

Professional Requirements:

• B.Tech (Electronics/Electrical/Mechanical) with 4-7 years of experience in Quality / Engineering / Manufacturing environment, preferably from medical industry with ISO 13485 auditor certification is a must.

• Intermediate level ability to use most MS tools (Word, Excel, PowerPoint, etc.)

Technical Competencies

• Supplier Quality Processes/ Tools - Working knowledge of basic and advanced Quality tools such as; Six Sigma, SPC, FMEA, Control Plans, Root Cause Analysis, Poke Yoke, Kaizen, Lean Manufacturing etc.

• Executes/ Masters & implements/ improve all supplier quality tools/ Processes . Trains supplier in these tools effectively.

• Commodity Domain Knowledge – Strong Knowledge & understands technology, regulatory requirement related to product, system & services. Determine supplier technical abilities based on these knowledges.

Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.