Shipping Coordinator I
Charles River Laboratories International Inc (CRL)
Mattawan, MI, US, 49071
Job Summary
SALARY: The hourly rate for this position is a flat rate of $20.00. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.
SHIFT: Monday - Friday, 8:00am - 4:30pm
Central shipping supports the transfer of generating, organizing, and verifying, and general oversight of materials shipped. Staff manages shipping materials related to biological specimens, test article, formulation samples and multiple other study materials. Staff also supports the shipping process by maintaining shipment status within the proper shipping system. Staff are knowledge in application of GxPs and applicable SOPs, U.S. Department of Transportation (DOT)/International Air Transportation Association (IATA) regulations, along with adhering to study protocols to accurately ship materials.
Essential Functions (The fundamental Competencies/Skills & Responsibilities of the role (products and services provided/results accomplished) include, but are not limited to, those listed: • Efficiently performs and documents all procedures, materials, and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.) • Demonstrates effective teamwork, and communication skills through informal discussions with peers, supervisor, and team • Accurately identifies and effectively communicates any regarding materials shipped/to be shipped • Maintains the integrity and security of archived materials, as applicable to the discipline • Effectively performs tasks including but not limited to generating, organizing, and verifying shipping documents, and packaging material in accordance with DOT/IATA regulations, and processes shipments with courier services, with oversight • Develops knowledge for one operational area of shipping, with oversight • Develops critical thinking, troubleshooting and time management skills aligned with the needs of the discipline • Perform all other related duties as assigned
Job Qualifications
Qualifications (Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to: • HS/GED/Associate’s degree or equivalent experience. No previous experience required • An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above • Ability to communicate verbally and in writing at all levels inside and outside the organization • Basic familiarity with Microsoft Office Suite • Computer skills, commensurate with Essential Functions, including the ability to learn a validated system • Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice • Ability to work under specific time constraints
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 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 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.
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 [email protected]. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
Job posted: 2024-06-21
