Laboratory Assistant I
About the role
Perform basic laboratory support and record-keeping tasks.
Responsibilities
- Receive, monitor, and maintain inventory and stock levels of assigned areas.
- Operate lab equipment and perform routine maintenance as needed.
- Prepare lab solutions (e.g., buffers, media/common vehicles, and bleach solutions).
- Wash and dry glassware and distribute to appropriate locations within the laboratory.
- Keep glass-washing area clean and organized.
- Sterilize glassware and other items using an autoclave.
- Label tubes and perform laboratory set-up/clean-up.
- Organize and perform inventory of department refrigerators or freezers.
- Assist in the archiving of equipment/facility records.
- Assist technical personnel with clerical duties (e.g., filing, making copies, shipments set-up etc.).
- Record observations and measurements for basic lab/research tasks.
- Perform limited troubleshooting and maintenance of instruments as appropriate for assigned area.
- Generate forms, tables, and hand record data.
- Perform all tasks in compliance with Good Laboratory Practice Regulations (GLPs) and Standard Operating Procedures (SOPs).
- Ship, store, and document received supplies (e.g., test articles, bio-hazard boxes, dry ice, reagents, etc.).
- Assist technical personnel with laboratory supplies expiry check and discard as needed.
- Perform all other related duties as assigned.
Requirements
- High school diploma or General Education Degree (G.E.D.).
- Valid, state-issued, driver’s license.
- Detail-oriented with general familiarity with lab procedures.
- Good verbal communication skills.
- Basic computer skills; familiarity with Microsoft Office software.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Pay
The pay for this position is between $20.00 - $21.00/hour. Salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.
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 worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.