Manufacturing QA Engineer

at  Agilent Technologies Inc

WE ARE LOOKING FOR A NEW TEAM MEMBER. JOIN US!

Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications, and expertise. Agilent enables customers to gain the answers and insights they seek - so they can do what they do best: improve the world around us. Information about Agilent is available at www.agilent.com.
We are looking for a Manufacturing Quality Engineer to help us become even better in what we do. We are offering a phenomenal opportunity to contribute with ideas and have an influence on how we develop the future. You will be joining a collaborative team ready to share their knowledge and help you build your knowledge through support and comprehensive training.
With reference to our Manufacturing Quality Engineer, you will be part of a team that is responsible for ensuring products are manufacturing to the highest quality standards, while partnering with a dynamin manufacturing and R&D team.

QUALIFICATIONS:

• Bachelor’s or master’s degree in a technical discipline.
• +2 years of work experience in the medical device or pharmaceutical industry
• Experience working with In Vitro Diagnostic and/or Medical Devices
• Good knowledge of Medical Device and In-vitro Diagnostic Standards and Regulations. Including, ISO 13485, IVDR Regulation (EU) 2017/746, ISO 14971 and the Regulations governed by Medical Device Single Audit Program (MDSAP).
• Strong verbal and written communication skills
• Full fluency to read/write/speak in English on a business level.
• Detail oriented as well as a proactive team player who’s capable of independently working cross-functionally with people at all levels of the organization.

• Play a pivotal role in the Non-conforming (NC) and Corrective and Preventive Action (CAPA) programs. Drive, teach, and mentor peers to ensure thorough investigations, root cause analysis, corrective/preventive actions, and verification plans occur.
• Lead and drive a collaborative culture that shares best practices, proactively partners across the organization, and mentors team members on Quality principles (both within and outside Quality).
• Apply advanced Quality Engineering techniques, such as statistical process controls and sample plans, to drive proactive Quality improvements.
• Lead complex projects from initiation to completion, while planning for resource needs, identifying compliance needs, collaborating with internal partners/stakeholders and proactively providing solutions.
• Integration of the principles of Lean methodology (GEMBA, Kaizen, Tier Metrics, etc.) to drive overall systemic Quality improvements.
• Work independently, or with teams, to find solutions to manufacturing quality related opportunities.