Essential Responsibilities
* Perform dose formulation analysis in support of GLP Toxicology assays
* Perform method validations for HPLC and correlating stability studies for analysis of test articles or other chemicals.
* Setup, maintenance and daily operation of HPLC system and related equipment.
* Aid in the writing and editing of analytical and formulation sections within protocols and reports.
* Prepare reagents, vehicles, solutions and suspensions following applicable SOPs, Protocols, and GLPs.
* Receipt of controlled and non-controlled chemicals
* Assures proper labeling, handling, and storage of all chemicals.
* Maintain up-to-date chemical inventory
* Perform solubility testing
* Perform dose formulation calculations and preparations
* Ensure chemical disposal is handled per local, state, and federal regulations
* Communicate with Study Directors, Program Managers, and analytical labs to ensure adherence to study protocols
Additional Responsibilities
* Prepare dose formulations for in vitro and in vivo experiments as needed
* Training of junior staff as needed.
* Work in a team environment with a professional and positive attitude
* Other duties as needed
Minimum Acceptable Qualifications
* Education:
o B.S. in chemistry or related field
* Experience:
o Two years' experience in a GLP scientific environment
* Skills:
o Ability to perform basic unit conversion calculations
o Experience working under GLP or regulatory requirements
o Ability to use, troubleshoot, and maintain standard chromatography laboratory equipment.
o Excellent written and oral communication skills
o Excellent computer skills working with MS Word/Excel/Powerpoint
o Attention to detail
o Excellent organizational skills
o Ability to exercise independent judgment
*This position could be offered at different levels for candidates who qualify with a combination of advanced levels of education and/or years of experience. The salary range will adjust along with the level of the role to match the person's relevant experience and/or education level.
Inotiv is a growing contemporary drug discovery and development company where we "Play to Win" in an industry rich with opportunity. Together, we face challenges and together we win in the delivery of world-class drug discovery and development solutions that impact the health and well-being of people all over the world. There's an opportunity for everyone at all phases of a career, each individual's unique skill set has an impact on the work we conduct. If you have the talent and desire to impact the quality of people's lives, we have the career opportunities to make it happen. Join us in embracing research and science to impact the health and well-being of people all over the world.
Salary will be commensurate with experience and responsibilities. Benefits include health and dental coverage, short- and long-term disability, paid time off, paid parental leave, 401K, and more!
Inotiv is an Equal Opportunity Employer. It is our policy to provide a fair and equal employment opportunity to all persons, regardless of age, race, color, religion, sex, gender, gender identity, gender expression, sexual orientation, genetic information, disability, national origin, veteran status, or any other basis prohibited by law. This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination and access to benefits and training.
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