For 70 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.
We are seeking an Quality Assurance Auditor 1 for our Biologics Testing Solutions site located in Malvern, PA.
This position will perform audits of basic records and reports and inspections of routine processes to assure compliance with
applicable regulatory requirements, international standards, and corporate policies and procedures.
The following are responsibilities related to the Quality Assurance Auditor 1:
• Perform GMP data and document (SOPs, protocols/batch records) reviews to assess that records follow ALCOA+ and are in
compliance with all applicable regulations, international standards, and corporate policies and procedures.
• Provide Quality Assurance support to Operational laboratories including, but not limited to: room clearances, product and raw
material inspections and release, training, and facility inspections.
• Participate in development of corrective and preventative actions and process improvements in response to client and regulatory audits.
• Perform all other related duties as assigned.
The following are minimum requirements related to the Quality Assurance Auditor 1 position:
• Education: Bachelor’s degree (B.A./B.S.) or equivalent, preferably in a life science or related discipline.
• Experience: 1-2 years’ experience in a QA role; an equivalent combination of education and experience may be accepted as a satisfactory
substitute for the specific education and experience listed above.
• Certification/Licensure: None.
• Other: Knowledge of Microsoft Office applications (e.g. Word, Access, Excel). Must be able to comprehend regulations and guidance
documents and apply critical thinking skills to evaluate requirements. Must be detail oriented and able to effectively communicate verbally and in writing.
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 characterization, 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 17,000 employees within 90 facilities in 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. And in 2018, revenue increased to $2.62 billion.
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 ~85% of the drugs approved by the FDA in 2019.
Equal Employment Opportunity
Charles River Laboratories is an Equal Opportunity Employer – M/F/Disabled/Vet