Medical Technologist Associate Microbiology

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 Medical Technologist Associate to work in the Bacteriology Department at our Wilmington, MA location.

This individual is responsible for the effective processing and reporting of both internal and external samples for microbiological identification. They are expected to train microbiology staff as directed as well as maintain controlled documents to describe procedures.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

• Proficient in processing rodent, simian and environmental samples

• Reconcile customer paperwork with submission documentation to ensure accuracy

• Operate, maintain and perform troubleshooting procedures on microbiology analyzers and equipment

• Be proficient in the use and maintenance on all microbiological equipment in laboratory

• Prepare and label media, and supplies to support laboratory work and sample processing

• Proficient in proper media incubation location and time

• Obtain bacterial identification using MALDI-TOF, VITEK2 and biochemical tests as needed

• Perform antimicrobial susceptibility testing

• Document results to include creating orders and results data entry into results database in a timely fashion

• Communicate results, and clearly describe processes to internal and external clients

• Troubleshoot laboratory problems as tasked by management or Scientific Staff

• Collect and/or process samples according to departmental SOPs

• Maintain proper handling and inoculation techniques for media

• Work in a structured and regulated environment

• Work productively in group situations as well as independently

• Report all departmental exceptions to the manager or designee as instructed

• Provide leadership during training and motivation to all departmental personnel

• Share responsibility for departmental housekeeping and adherence to established safety procedures

• Maintain proficiency in all related department SOPs, policies, protocols and general knowledge of related laboratory processes

• Review and edit departmental SOPs and forms

• Train all new hires on departmental needs and expectations

• Organize and train Laboratory Technicians I and II

• Maintain up to date training records on all procedures and protocols applicable to work duties

• Perform and document internal qualification of new techniques and procedures under the guidance of management or Scientific Staff

• Adhere to all departmental SOPs, policies, safety procedures and protocols

• Remain organized in a fast-paced environment

• Perform all other related duties as required

MINIMUM QUALIFICATIONS:

• Bachelor's degree (B. S. ) or equivalent in biological sciences or related discipline

• A minimum of 2-3 years of experience in a clinical laboratory environment (using WASP/MALDI-TOF, VITEK2)

• 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

• An attention to detail and accuracy

• Effective verbal and written communication skills

• Must have the ability to communicate effectively in a small group or one-on-one setting

• Proficient in Computers (IE Basic skills in MS Office Suite)

PREFERRED QUALIFICATIONS:

• MT or MLT with certification or certification-eligible (ASCP or HEW)

• 6 months or more of training experience

• Leadership skills

The hourly pay range for this position is $26. 00 - $33. 00. 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 Opportun.