Quality Control Specialist

at  Stryker

San Jose, CA 95138, USA -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate09 Nov, 2024USD 26 Hourly10 Aug, 20242 year(s) or aboveGood communication skillsNoNo
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Description:

We are excited to be named one of the World’s Best Workplaces by Fortune Magazine! We are proud to offer you 12 paid holidays annually. For an overview of our benefits and time off, please follow this link to learn more:US Stryker employee benefits.
Work Flexibility: Onsite
On Site Location: 5900 Optical Ct., San Jose, CA
Shift: Monday - Friday, 7:30 AM - 4:00 PM
Starting Pay: $26.60/hr.
Come join Stryker, one of the world’s leading medical technology companies who, together with our customers, is driven to make healthcare better. We offer innovative products and services in Medical and Surgical, 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.
We are proud to be named one of the World’s Best Workplaces and a Best Workplace for Diversity by Fortune Magazine!

Responsibilities:

The Quality Control (QC) specialist of a service team meets goals for the repair and processing of medical devices. They ensure all consoles/devices are within specifications according to FDA and Stryker standards prior to departing the Stryker facility and sent to hospitals. Additional responsibilities may require you to:

  • Meet daily with both the team leads and supervisor to provide their daily plan and priorities, along with obtaining the daily goals set by the team lead.
  • Support production, business, and other processes in a team-based manufacturing environment.
  • Inspect various medical equipment on all production lines within FDA/Stryker standards.
  • Perform activities in production planning, quality management, equipment management and new process implementation.
  • Ensure products are reviewed properly and complete inspections of medical devices.
  • Assist engineers in training of core skill areas, and interact with supervisors and customer service to problem solve and improve processes.
  • Perform packaging line, income and/or manufacturing inspections of mechanical and electro/mechanical products and/or components.
  • Ensure raw materials in process and/or finished products meet company and FDA standards, using engineering schematics or blueprints to perform accurate checks and tests
  • Inspect packaging and/or labeling and literature to ensure regulatory compliance; assist in devising standard and non-standard inspection procedures.


REQUIREMENT SUMMARY

Min:2.0Max:7.0 year(s)

Hospital/Health Care

Pharma / Biotech / Healthcare / Medical / R&D

Health Care

Diploma

Proficient

1

San Jose, CA 95138, USA