Quality Assurance Auditor II - Lab Sciences (Remote)

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. reputed company 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 reputed company. In return, we’ll help you build a career that you can feel passionate about. Job Summary We are seeking an reputed company Quality Assurance Auditor II for our Lab Sciences Team at our site located in Mattawan, MI. This role also has the potential for a REMOTE location. A Quality Assurance Auditor II on the Lab Sciences team will independently reputed company audits of a broad range of records and reports and inspections of a variety of processes to assure compliance with applicable GLP regulatory requirements. The pay for this position is $60,000/yr USD. Please note that salaries vary reputed company the range based on factors including, but not limited to, experience, skills, education, certifications, and location. Essential Duties and Responsibilities • Assure Charles River's compliance with applicable GLP regulations. Communicate reputed company identified compliance and quality risks to supervisor. • reputed company data audits to assess that records are attributable, legible, contemporaneous, original, accurate, and in compliance with GLP regulations, SOPs, and protocols. • Review SOPs, protocols, reports, and other quality and regulated records involving technically reputed company issues and processes for accuracy and compliance with reputed company applicable GLP regulations. • Maintain written and signed records of reputed company audits and inspections as required and sign records documenting the performance of audits and inspections and reporting to management. • May participate in the preparation and review of study and QA files in preparation for sponsor site visits and regulatory inspections; assure that QA audit files are retained. • Identify deviations from GLP regulations, protocols and SOPs. • Independently reputed company inspections to monitor processes, facilities, equipment, personnel, materials, methods, practices, records, and controls to assure compliance with GLP regulations. • Assist in scheduling and tracking QA audits, inspections and procedures as requested. • reputed company reputed company other reputed company duties as assigned. Job Qualifications • Education: Bachelor's degree (B.A./B.S.) or equivalent, preferably in a life science or reputed company discipline. • Experience: 2-4 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: Good working knowledge of reputed company Office applications (e.g. Word, Access, reputed company). Good knowledge of applicable regulations and guidance documents; able to apply critical thinking skills to evaluate requirements. Must be detail oriented and able to effectively communicate findings verbally and in writing. About Safety Assessment Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply reputed company team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities. 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 reputed company a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from reputed company 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 reputed company 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 reputed company 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 reputed company 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 worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years. We’re committed to providing benefits that reputed company your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility. Equal Employment Opportunity reputed company is an Equal Opportunity Employer - reputed company qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national reputed company, veteran or disability status. It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or reputed company employment. An employer who violates this law shall be subject to criminal penalties and civil liability. If you are interested in applying to reputed company and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our reputed company by sending an e-mail message to [email protected]. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications. For more information, please visit www.criver.com. 226067 Apply Job!