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Formulations Logistics Coordinator
Charles River Laboratories International Inc (CRL)
Horsham, PA, US, 19044
IMPORTANT: In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process. Please make sure work history and education are added correctly.
Job Summary
Manage the receipt, inventory and shipment of test materials and reagents ensuring compliance with Good Laboratory Practice (GLP), study protocols, and Standard Operating Procedures (SOPs).
ESSENTIAL DUTIES AND RESPONSIBILITIES: • Manage receipt of test materials and facility reagents including documentation of test material receipt according to facility SOPs • Maintain inventory of test materials and facility reagents within storage locations • Ensure Certificate of Analysis (COA) and Safety Data Sheets (SDS) are received for all materials and stored appropriately • Ensure Occupational Exposure Band (OEB) ranking or Biological Risk Assessment is conducted for all received test material, as appropriate • Assist in coordinating and resolving any deficiencies in shipping paperwork with clients, brokers, third party shippers to ensure timely receipt of test materials • Prepare shipping paperwork, package samples of formulations and test material and coordinate with shipping department for timely shipments • Order required supplies and reagents as needed and maintain inventory • Assist with Controlled Substance Control and inventory • Maintain Hazardous Chemical inventory • Ensure compliance with all applicable local, state, and federal regulations, including but not limited to GLP, FDA, DEA, IATA and OSHA • Any other duties as assigned
Job Qualifications
• Education: Bachelor’s degree (B.A./B.S.) or equivalent in life sciences or related discipline required • Experience: 1-2 years related experience in a CRO, bioanalytical or chemistry lab required • 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: Ability to organize, prioritize work and meet deadlines. Computer literacy including word processing, databases and spreadsheet software. GLP experience preferred.
IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.
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 experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 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 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 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.
Equal Employment Opportunity Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
If you are interested in applying to Charles River Laboratories 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 Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
Job posted: 2023-02-25
