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Surgical Diagnostic Associate I

Charles River Laboratories International Inc (CRL)

Mattawan, MI, US, 49071

Job Summary

We are seeking an experienced Surgical Diagnostic AssociateI for our Surgery (OR) Team at our Safety Assessment site located in Mattawan, MI.

A Surgical Diagnostic Associate I regularly performs basic imaging using diagnostic equipment for all applicable species with minimal supervision. The individual in this role may also document setup, provide quality control for procedures, and administer procedural anesthesia for all species, as well as operate and maintain specialty equipment such as imaging equipment or other diagnostic equipment with little supervision.

Essential Functions:

  • Ensure welfare and humane care for all animals worked with through gentle, positive human-animal interactions.
  • Operate diagnostic equipment, maintain, and troubleshoot instrumentation and equipment with minimal supervision.
  • Occasionally perform basic skills of department, with minimal supervision. Skills may include animal handling/restraint, housing, and maintenance, feeding procedures, collecting data, and observing the animals for health status.
  • Document processes and provide timely analysis of study data.
  • Serve as liaison with contractors.
  • Provide general support to technical staff.
  • Conduct peer review of imaging and data integrity for quality control.
  • Perform specific imaging or diagnostic tasks, based on department training plans.
  • Collect, document, review, and verify data on forms, or in electronic data capture systems, as required/applicable.
  • Review documentation of functions performed as part of quality control requirements.
  • Maintain procedure room and stock lab supplies.
  • Perform all other related duties as assigned. 

The pay range for this position is $22.50 - $24.00/hour USD.  Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

Qualifications:

  • Education: High school diploma or General Education Degree (G.E.D.) required. Bachelor's degree (BA/BS) or equivalent in a biological science, preferred.
  • Experience: 2 years of relevant experience.
  • An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
  • Certification/Licensure: Functional certification preferred. 
  • Skill plan completed for this role based on department training plan.
  • Demonstrated ability to consistently and effectively produce high quality results, interpret protocol requirements, troubleshoot quality issues, and record accurate study and departmental data.
  • Ability to communicate verbally and in writing at all levels inside and outside the organization.
  • Excellent written and verbal communication skills. 
  • Ability to manage multiple tasks and priorities to achieve goals.
  • Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
  • Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
  • Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
  • Ability to exercise independent decision-making and self-manage under the direction of a supervisor.
  • 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: 2024-02-22

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