For 75 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.
Job Summary
We are seeking a
Laboratory Technician to work at our
Serology Department at our Wilmington, MA location.
The
Laboratory Technician is responsible for the effective processing and reporting of both internal and external samples by various serologic assays as specified by departmental SOPs.
Essential Duties And Responsibilities
- Under direct supervision, perform laboratory activities including but not limited to reagent preparation, laboratory maintenance/monitoring and routine testing of client samples by the various serologic methods in compliance with departmental SOPs
- Reconcile customer paperwork with submission documentation to ensure accuracy
- Assist in the receipt of samples to be tested
- Document sample receipt using the Central Receipt database
- Knowledge of various sample types and storage conditions
- Follow instructions on sample submission forms for sample organization
- Knowledge of proper sample dilution technique
- Transfer samples to holding plates either manually or with the aid of a sample transferring device
- Perform at least one serologic assay
- Operate and maintain pipettes
- May assist in the preparation of departmental media and diluents, including knowledge of proper labeling technique and storage conditions
- Share responsibility for maintaining appropriate inventory levels of departmental supplies
- May prepare samples for additional testing in another lab within the company or for an outside source
- Document results to include creating orders and results data entry into laboratory database in a timely fashion
- Collect and/or process samples according to departmental SOPs
- Ability to work in a structured and regulated environment
- Work productively in group situations as well as independently
- Assist in reporting departmental exceptions to the manager or designee as instructed
- Share responsibility for departmental housekeeping and adherence to established safety procedures
- Responsible for proficiency in all related department SOP’s, with general knowledge of the laboratory processes
- Maintain skills in using computer programs such as Microsoft Word, Microsoft Excel and others as the need arises
- Maintain up to date training records on all procedures and protocols applicable to work duties
- Adhere to all departmental SOPs, policies, safety procedures and protocols
- Remain organized in a fast-paced environment
- Perform all other related duties as assigned
Minimum Qualifications
- Bachelor’s degree (B.S.) or equivalent in biological sciences or related discipline
- 0 to 2 years related technical experience in a Pharmaceutical, Biotech, or Contract Research Organization laboratory environment
- An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
- Strong organization and prioritization skills.
- Attention to detail and accuracy.
- Effective verbal and written communication skills.
- Communicate effectively in a small group or one-on-one setting.
- Proficient in Computers (ie: Microsoft Office Suite).
Preferred Qualifications
- Experience in immunoassays including knowledge of basic immunoassay methods and ability to operate typical laboratory equipment, specifically pipettes, spectrophotometer, centrifuges, microscopes and other laboratory equipment.
The hourly pay range for this position is $22.00 - $23.50. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.
About Research Models & Services
Fundamental to basic research and discovery is the use of in vivo models to help identify disease targets and determine potential biological pathways that regulate the condition. As the world’s leader in the production and distribution of the highest quality research animal, with 1 out of 2 animal models produced for preclinical research globally, we understand the importance of this step. With seven decades of experience, our expertise is unmatched, allowing us to provide you with the perfect model, including disease-specific and preconditioned options, for basic research and beyond.
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.
We’re committed to providing benefits that elevate 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
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.
It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
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.
For more information, please visit www.criver.com.
225681
