Quality Auditor

Details of the offer

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies.
When you join our family, you will have a significant impact on the health and well-being of people across the globe.
Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform.
In return, we'll help you build a career that you can feel passionate about.
Job Summary We are seeking an experienced Quality Auditor for our Biologics Division located in Ballina, Co. Mayo, Ireland .
This role shall report to the QA Manager and the main duties & responsibilities shall be: Perform general auditing duties for compliance with quality standards.
Prepare written reports on audit and inspection activities.
Review SOPs.
Assist in the administration of the Quality Department and of Quality systems.
Assist with Vendor Assessment, client audits and subcontractor audits.
Job Qualifications The following are minimum requirements related to the Quality Auditor position.
BSc.
in a Science discipline Established experience of working within a GLP/GMP environment is preferable, but not essential to the role Previous quality auditing experience preferable.
Meticulous attention to detail and high level of accuracy.
Comfortable working with calculations.
Ability to work both individually and within a team Excellent interpersonal & communication skills both written and verbal.
IT Skills – MS Word, Excel, PowerPoint.
About Biologics Testing Solutions With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide.
Offering a variety of services such as contamination and impurity testing, protein characterzation, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products.
Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs.
Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.
About Charles River Charles River is an early-stage contract research organization (CRO).
We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development.
Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities.
Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges.
Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
At Charles River, we are passionate about our role in improving the quality of people's lives.
Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe.
We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.
At Charles River Laboratories, we recognize and recruit all talent.
We are a company committed to the principle of diversity and inclusion and work daily in this direction.


Nominal Salary: To be agreed

Source: Talent_Ppc

Job Function:

Requirements

Validation Supervisor

We Make Life More Rewarding and Dignified  Location: Ballina  Department: Quality    Summary: The primary purpose of the Continence Care Validation Superviso...


Hollister Incorporated - County Mayo

Published a month ago

Spuiter Bij Autoschade Herstel Roos

Ben jij een vakman die kwaliteit op nummer één heeft staan? Dan is de functie van Spuiter bij Autoschade Herstel Roos echt iets voor jou! Als Spuiter heb je ...


Toppa Nederland - County Mayo

Published 17 hours ago

Supplier Quality Auditor

McKesson is an impact-driven, Fortune 10 company that touches virtually every aspect of healthcare. We are known for delivering insights, products, and servi...


Mckesson - County Cork

Published 23 days ago

Uat Analyst (6-Month Maternity Leave)

The Company Founded in 2009, Cubic Telecom has grown to become one of the leading providers of connectivity solutions and analytics services that help vehicl...


Cubic Telecom - County Dublin

Published 23 days ago

Built at: 2024-11-21T16:41:39.580Z