Sr. Associate Sterilization Engineering - Scottsdale

This is an onsite position requiring the team member to be onsite 5 days a week. This position offers relocation assistance. · Responsible for the development and execution of sterilization strategies to ensure medical devices meet functionality and design standards. · Perform ri ...

For this onsite position, employee will serve as resource to project teams to support all sterilization-related activities as it relates to research and development of health care products. · ...

We're a dedicated team that is connected by a purpose to improve patient lives. A name started our story. How will yours help write our future? · There's no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and developme ...

For this onsite position employee will serve as resource to project teams to support all sterilization related activities as it relates to research and development of health care products Contribute to identification and selection of appropriate sterilization technology and manag ...

For this onsite position, employee will serve as resource to project teams to support all sterilization-related activities as it relates to research and development of health care products. · ...

The Regulatory Affairs Specialist role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions and documentation for other international regulatory bodies. · Responsible for managing and preparing 510(k) submissions to obtain FDA clear ...

The Regulatory Affairs Specialist role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions and documentation for other international regulatory bodies. This position requires a minimum of five years medical device regulatory experi ...

· At West, we're a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government du ...

Plan, direct and supervise operations production processes and personnel within the proprietary product value streams in Operations. · ...

We're looking for a Production Supervisor to join our team at West Pharmaceutical Services Inc. You will plan direct supervise operations production processes and personnel within the proprietary product value streams in Operations under appropriate guidance leadership. · ...

Job summaryLensas is a career site that helps job seekers find great jobs in the US and does not hire directly for these jobs but promotes them on LinkedIn behalf of its direct clients recruitment ad agencies marketing partners. · ...

Plan direct and supervise operations production processes and personnel within the proprietary product value streams in Operations under appropriate guidance and leadership. · ...

+Job summary · The Regulatory Affairs Specialist role is responsible for preparing and submitting documentation for FDA 510(k) submissions.++•Ability to work in a fast paced collaborative team environment+•Ability to handle multiple projects and coordinate cross functional teams+ ...

The Regulatory Affairs Specialist role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions. · ...

Responsible for Test Method Validations, conducting investigations, assists in the investigation of design and manufacturing issues. · ...

Assist in new process development for new or existing medical devices and processes. · ...

Create quality standards and procedures in accordance with established Erbe Quality system. · Implement and evaluate changes to existing processes designed to improve product quality. · ...

This position is responsible for contributing to the development implementation and execution of the full product lifecycle quality management program at Erbe.The job duties include creation and collaboration on design process risk management measurement systems analysis design v ...

This is a technical role assisting and leading R&D engineer medical device testing. · Experience working in a laboratory or controlled manufacturing environment; knowledge of good documentation practices. · ...

Join one of our growing Medical Device/Manufacturing clients in Tempe, AZ as Supply Chain Planning Lead to plan and prepare production schedules for device components manufacture. · ...