Operator II - Production Operations (Second Shift) at Cordis

Santa Clara, California, United States -

Full Time

Start Date

Immediate

Expiry Date

28 Jul, 26

Salary

0.0

Posted On

29 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Manufacturing, Quality Systems, GMP, GDP, Microscope operation, Cycle time management, Attendance, Safety compliance, 5S principles, Hand-eye coordination, Communication skills, Inventory control, Polymer forming, Tip forming

Industry

Medical Equipment Manufacturing

Description

Overview When you join the team at Cordis, you become part of an inspiring mission to save lives, impacting millions of people and broadening access to life-saving cardiovascular and endovascular technology. As a global leader for over 60 years, we are dedicated to being the heart of innovation to transform cardiovascular care. At Cordis, we're teammates, not just employees. We embrace an empowered and one-team culture where teammates are inspired to unleash their full potential. With diverse teams on a global scale, we believe the richness of our experiences and backgrounds enhances the careers of our teammates, the service to our customers, and ultimately, the lives of our patients. If you love a challenge and are ready to have a direct, transformative and positive impact on the lives of millions, then Cordis is just the place for you. We are the people behind the people who keep saving lives. Responsibilities The 2nd shift Operator II - Production Operations is responsible for building product by following all Quality Systems and Processes (in which trained and certified to) and complete other assigned tasks while meeting manufacturing goals and metrics. Adheres to all Quality Policies and Systems of the Company Maintains accurate records, including Lot History Records (LHR), and adheres to all GMP/GDP policies Must be able to process small parts under a microscope Consistently meets (or may occasionally exceed) the average cycle time and quality standard requirements for the stations/processes trained/certified to Maintains an acceptable level of attendance (including scheduled overtime) Maintains a professional work relationship with other team members and other cross‐functional groups Able to flex and rotate to other stations as necessary Understands and follows safety policies and practices, and escalates any issues related to product quality or workplace safety Follows and adheres to 5S principles and goals Qualifications High school diploma or equivalent and 2‐5 years experience in the medical device/pharmaceutical field or in a related area Must be able to work in a Controlled Environment Room Must have good hand‐eye coordination Must have good verbal and written communication skills Demonstrates reading, writing, and math & inventory control skills (with respect to accuracy and counts) Polymer and/or tip forming experience a plus

Responsibilities

The Operator II is responsible for building medical device products while strictly adhering to quality systems, GMP/GDP policies, and manufacturing metrics. They must maintain accurate production records and rotate between various manufacturing stations as required.