Julia Garner

Julia Garner

Instrument And Compliance Coordinator @ Bristol Myers Squibb

About Julia Garner

Julia Garner is an Instrument and Compliance Coordinator at Bristol-Myers Squibb in Moreton, UK, with extensive experience in analytical and quality assurance roles.

Title and Company

Julia Garner currently holds the position of Instrument and Compliance Coordinator at Bristol-Myers Squibb in Moreton, UK. In this role, she is integral to the company's quality and compliance operations.

Professional Experience

Julia Garner has extensive experience in the pharmaceutical industry. She began her career at GSK as an Analytical Scientist from 1988 to 1992 in Worthing, West Sussex. She then transitioned to Seton Health Care as a Quality Assurance Analyst, a position she held from 1992 to 1998 in Bootle, Merseyside. Julia joined Bristol-Myers Squibb in 1998 as an Analytical Scientist in Merseyside, serving in the role for 14 years until 2012. Following this, she worked as a Stability Scientist at Bristol-Myers Squibb from 2012 to 2017 before assuming her current role.

Educational Background

Julia Garner completed her education at notable institutions. She studied at the University of Brighton from 1991 to 1992 and later pursued further education at Liverpool John Moores University from 1993 to 1994. Her academic background has fortified her expertise in the pharmaceutical field.

Role Responsibilities at Bristol-Myers Squibb

In her current role at Bristol-Myers Squibb, Julia Garner is responsible for instrument validation and approval of instrument calibrations. She is also involved in completing Infinity instrument change management records and conducting root cause analysis for investigations. Additionally, she facilitates quality risk management activities and monitors compliance, ensuring adherence to industry standards and protocols.

Authorship of Instrument Validation Documents

Julia Garner has authored numerous instrument validation documents during her tenure. Her expertise in this area is evident through her detailed and compliant documentation, which is crucial for maintaining the integrity and precision of pharmaceutical instruments.

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