Job description
Overview:
Join us in embracing research and science to impact the health and well-being of people all over the world. Responsibilities:
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, gender, gender identity, sexual orientation, 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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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.
- Method development, experimental design, and study conduct to evaluate concentrations of potential drug substances by chromatography/mass spectrometry.
- Serve as Inotiv representative and point of contact to Study Directors and/or Sponsors for bioanalytical projects. This includes documenting Study Director/client exchanges (including phone conversation, emails, etc.).
- Establish the experimental design and manage the conduct of studies in compliance with the protocol/amendments/planned changes, Best Practice Documents and SOPs.
- Operate analytical instrumentation and lab equipment and perform analyses according to the Operation Manuals, SOPs, and/or Best Practices.
- Review literature to determine appropriate approach for project-specific bioanalytical needs.
- Consult with Operational Management to determine the availability of resources prior to initiation of study activities and during the project as needed.
- Assure necessary personnel (e.g. QAU, Study Director, etc.) are aware of any deviations from the study protocol/Best Practice Documents and/or SOPs during the course of a study and ensure that proper documentation is performed.
- Provide leadership, management, training, and mentoring of direct reports and colleagues, to enhance their skills and knowledge, as appropriate.
- Generate and report results accurately and within defined timelines. Ensure any deviations are reflected as appropriate.
- Assure that study data and samples are compiled, organized, inventoried, and archived at Inotiv or transferred to the testing facility archive/client, or disposed, prior to or upon completion of the services, as applicable.
- Demonstrate an understanding of Best Practices, SOPs and Good Laboratory Practice Regulations (21 CFR, Part 58) as these relate to study-specific services provided, this job description, and general facility operations.
- Perform all other duties and responsibilities of Principal Investigator when assigned as defined in applicable SOPs
- Interact with clients, other employees, and the community in a professional manner
- Support and participate in departmental and company initiatives
- Perform other duties as assigned
- BS or equivalent degree in Chemistry, Biochemistry, or related field, and greater than 15 years qualified experience in vitro/in vivo Drug Metabolism studies, or
- MS in Chemistry, Biochemistry, or related field, and at least 10 years qualified experience with in vitro/in vivo Drug Metabolism studies, or
- PhD in a Pharmaceutical-related science with full knowledge and post-doctoral experience with in liquid chromatography-mass spectrometry LC-MS/MS, LC-HRMS
Preferred Skills and Abilities:
- In-depth knowledge and specific understanding of all the processes related to Bioanalysis and drug discovery and development
- Versatility and accuracy performing laboratory operations, some of which may be difficult and/or non-routine.
- Ability to use a computer to compile and maintain databases for records and inventory, utilizing the appropriate software.
- An attitude for quality, an eye for detail, the ability to follow written instructions and work with a minimum of supervision.
- A working knowledge and awareness of general laboratory procedures.
- Good written and oral communication skills.
- Ability to adhere to all safety regulations and procedures.
Inotiv has been named a 2023 Top Workplace!
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 participation with company match, 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, gender, gender identity, sexual orientation, 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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