Summary

Inotiv is a leading contract research organization (CRO) specializing in nonclinical research services for the pharmaceutical, biotechnology, and medical device industries. The company provides comprehensive solutions including discovery and safety assessment services, research models, and analytical support. Inotiv operates through two main segments: Research Models and Services (RMS) and Discovery and Safety Assessment (DSA). The RMS segment offers research models, including purpose-bred rodents and large research models, along with related services. The DSA segment provides drug discovery and development services, including in vitro and in vivo studies, bioanalytical services, and regulatory support. With facilities across North America and Europe, Inotiv serves a global client base, supporting the development of new therapeutics from early discovery through regulatory submission. The company plays a critical role in advancing biomedical research by providing essential preclinical data and models that help accelerate the development of new drugs and medical treatments.

Job description

Essential Position Responsibilities

Proficiency in the operation of laboratory's instruments for analysis of biological samples collected from laboratory animals for standard panels of clinical chemistry, hematology, coagulation and urinalysis.
Maintenance of laboratory instruments and equipment according to company SOPs.
Records observations and collects data via data capture systems, and/or hand generated forms in accordance with GLPs, SOPs, and protocol.
Independently reviews data, performs laboratory QC and identifies potential problems.
Communicates with the study directors and in-life technicians regarding sample quality.

Additional Position Responsibilities / Critical Success Factors

Performs general laboratory support functions such as supply inventory, shipping procedures, administration of computer systems or data maintenance.
Ability to multi-task and participate in multiple nonclinical research studies concurrently.
Ability to produce high quality data while working under the pressure of strict deadlines.
Overtime, weekend and holiday work may be required.
Work requires passing pulmonary function test, annual physical and the use of other PPE (personal protective equipment).

Qualifications

B.S. or B.A. preferred.
ASCP certification or equivalent is required.
Experience with sample analysis in Clinical Chemistry, Hematology, Coagulation and Urinalysis.
Knowledge of Good Laboratory Practices (GLP) preferred.

Requirements

ASCP certification or equivalent is required
Experience with sample analysis in Clinical Chemistry, Hematology, Coagulation and Urinalysis
Knowledge of Good Laboratory Practices (GLP) preferred
B.S. or B.A. preferred
Ability to multi-task and participate in multiple nonclinical research studies concurrently
Ability to produce high quality data while working under the pressure of strict deadlines
Work requires passing pulmonary function test, annual physical and the use of other PPE

Benefits

Health coverage
Dental coverage
Short-term disability
Long-term disability
Paid time off
Paid parental leave
401(k)

Company overview

Inotiv is a leading contract research organization (CRO) specializing in nonclinical research services for the pharmaceutical, biotechnology, and medical device industries. The company provides comprehensive solutions including discovery and safety assessment services, research models, and analytical support. Inotiv operates through two main segments: Research Models and Services (RMS) and Discovery and Safety Assessment (DSA). The RMS segment offers research models, including purpose-bred rodents and large research models, along with related services. The DSA segment provides drug discovery and development services, including in vitro and in vivo studies, bioanalytical services, and regulatory support. With facilities across North America and Europe, Inotiv serves a global client base, supporting the development of new therapeutics from early discovery through regulatory submission. The company plays a critical role in advancing biomedical research by providing essential preclinical data and models that help accelerate the development of new drugs and medical treatments.