Quality System Document Control

Other special projects and duties as assigned. Work with internal stakeholders to create, revise, review, and release requested documents.
** Minimum Requirements
*** Education and Experience
* Bachelor’s Degree, preferably in English or technical writing discipline, with minimum of 1 year work experience  2+ years direct work experience in technical writing or document management within a scientific and/or regulated industry.

Equivalent combination of related education and required work experience will be considered.

Ability to read, write, speak, and understand English.

Organized work habits and the ability to multi-task i

* Skills and Abilities

* Strong understanding of detailed requirements, methodology, and approach for managing and controlling documents within a formal QMSAbility to communicate and resolve document Ability to work on multiple tasks and prioritize work.

Excellent verbal and written communication skills.
** Working Conditions &

Physical Requirements
** Ability to read and interpret materials, verbally communicate, and hear required.  Able to communicate information and ideas clearly and articulately both in oral and written form. Uses appropriate language, style and methods depending on audience and the purpose of communication. Able to convey complex information clearly. Anticipates the information that others will need. Expresses ideas effectively.  Practices attentive and active listening.
** Improvement Driven.
** Inspires and generates new solutions and approaches to issues and challenges to maximize efficiency and effectiveness through everyday practice of root cause analysis and critical thinking problem solving;
Continually works to refine skills and abilities;
Builds on ideas of others to come up with new ways to address issues or problems;
Generates creative new solutions and approaches to issues and processes. ### Get In Touch Introduce yourself to our recruiters and we'll get in touch if there's a role that seems like a good match.

We’re looking for people who will help us grow and support our shared purpose: to help our clients discover and develop life-changing therapies for people around the world. As a leading contract research organization (CRO), Inotiv supports discovery and nonclinical development through investigational new drug (IND) and beyond. By leveraging our deep expertise and scientific capabilities, we help you increase efficiency, improve data, and reduce the cost of taking new drugs to market.

By providing critical research models and related services, we help researchers realize the full potential of their R&D projects, all while working together to build a healthier and safer world.  We hope you consider our opportunities and a future with Inotiv!
#J-18808-Ljbffr