The #1 Site for Finance Jobs - search all Finance jobs.
Mwy4x56vwqy3cn5jsz4

Agilent Senior RA/QA QMS Auditor

Description

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. The Agilent QMS Auditor is responsible for maintaining the Agilent QMS. The Agilent QMS includes products and processes associated with ISO 9001, ISO 13485 and various Medical Device regulations, including the Quality System Regulation (QSR) of the USFDA. Auditor responsibilities include:

  • Act as a focal point for assessments for a specific assigned business, region or function following all appropriate internal requirements
  • Uses the Audit Schedule to independently plan assigned assessments
  • Perform product, process, supplier and other assessments and complete and distribute assessment reports within 30 days
  • Verify closure of previous assessment findings
  • Summarize internal assessment findings
  • Educate others in quality and regulatory standards and consult in the development of processes and procedures consistent with those standards
  • Perform gap analyses for Business partners as needed
  • Keep skills current. Stay abreast of changing standards and regulations and share information as appropriate
  • Maintain external certification as a quality auditor from a recognized authority, e.g. ASQ/RAB
  • Participate in improvement efforts of the internal audit process
  • Assist Business Group QMS Manager with QMS activities and other tasks as requested
  • Attend required meetings, e.g. audit team, department meetings, etc.
  • Generate and distribute metrics illustrating effectiveness of the Internal Audit Program
  • Develop and manage travel schedules to ensure timely and effective audits for internal customers.
  • Facilitate conversations with Business RA and QA as needed
  • Collaborate with Agilent's medical device regulatory experts to ensure consistent regulatory interpretations, strategies and programs


Location -- Preferably Santa Clara, CA -- Will consider candidates from Austin, Texas, Wilmington Delaware, Colorado Springs, Colorado, Folsom or La Jolla, California (near a major Agilent facility)

Requirements

 

Job Snapshot

Location US-CA-Santa Clara
Employment Type Full-Time
Pay Type Year
Pay Rate N/A
Store Type QA - Quality Control, Finance, Science, Information Technology, Accounting
Apply

Company Overview

Agilent

As the world’s premier measurement company, Agilent works in close collaboration with engineers, scientists, and researchers around the globe to meet the communications, electronics, life sciences, and chemical analysis challenges of today and tomorrow. The company operates two primary businesses -- electronic and bio-analytical measurement -- supported by Agilent Laboratories, its central research group. Learn More

Contact Information

US-CA-Santa Clara
Snapshot
Agilent
Company:
US-CA-Santa Clara
Location:
Full-Time
Employment Type:
Year
Pay Type:
N/A
Pay Rate:
QA - Quality Control, Finance, Science, Information Technology, Accounting
Store Type:

Description

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. The Agilent QMS Auditor is responsible for maintaining the Agilent QMS. The Agilent QMS includes products and processes associated with ISO 9001, ISO 13485 and various Medical Device regulations, including the Quality System Regulation (QSR) of the USFDA. Auditor responsibilities include:

  • Act as a focal point for assessments for a specific assigned business, region or function following all appropriate internal requirements
  • Uses the Audit Schedule to independently plan assigned assessments
  • Perform product, process, supplier and other assessments and complete and distribute assessment reports within 30 days
  • Verify closure of previous assessment findings
  • Summarize internal assessment findings
  • Educate others in quality and regulatory standards and consult in the development of processes and procedures consistent with those standards
  • Perform gap analyses for Business partners as needed
  • Keep skills current. Stay abreast of changing standards and regulations and share information as appropriate
  • Maintain external certification as a quality auditor from a recognized authority, e.g. ASQ/RAB
  • Participate in improvement efforts of the internal audit process
  • Assist Business Group QMS Manager with QMS activities and other tasks as requested
  • Attend required meetings, e.g. audit team, department meetings, etc.
  • Generate and distribute metrics illustrating effectiveness of the Internal Audit Program
  • Develop and manage travel schedules to ensure timely and effective audits for internal customers.
  • Facilitate conversations with Business RA and QA as needed
  • Collaborate with Agilent's medical device regulatory experts to ensure consistent regulatory interpretations, strategies and programs


Location -- Preferably Santa Clara, CA -- Will consider candidates from Austin, Texas, Wilmington Delaware, Colorado Springs, Colorado, Folsom or La Jolla, California (near a major Agilent facility)

Requirements

 
Mwh1l46d5322gwvlk3l
MoneyJobs Advice

For your privacy and protection, when applying to a job online: Never give your social security number to a prospective employer, provide credit card or bank account information, or perform any sort of monetary transaction.Learn More

By applying to a job using moneyjobs.com you are agreeing to comply with and be subject to the workinretail.com Terms and Conditions for use of our website. To use our website, you must agree with theTerms & Conditionsand both meet and comply with their provisions.
Agilent Senior RA/QA QMS Auditor Apply now