Manufacturing QA Engineer

Job Description

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.

Key Responsibilities:

• Play a pivotal role in oversight of production-related changes, 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).
• 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.

We offer:

• An inspiring and social environment with around 40 skilled colleagues in the QA department providing QA support within development, manufacturing, and sustain activities.
• An opportunity to make a significant impact and develop your skills in a world-class company that takes pride in developing innovative solutions for pathology labs worldwide to improve cancer diagnostics.
• A role among passionate colleagues, in a growth-oriented and inclusive environment. You will become part of a caring and fast-paced environment, built on integrity, sharing, and trust.
• Core global benefits, including the Agilent Result Bonus and Stock Purchase Plan.

 Please note Job level will be adjusted according to relevant experience and qualifications.

Qualifications

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.

Additional Details

This job has a full time weekly schedule.

Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locations

Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.

Travel Required:

Occasional

Shift:

Day

Duration:

No End Date

Job Function:

Quality/Regulatory