Quality Assurance Auditor II page is loaded## Quality Assurance Auditor IIremote type : On-sitelocations : Mt. Vernon, INtime type : Full timeposted on : Posted Todayjob requisition id : JR100857 Inotiv , our work advances discoveries that improve lives—and our Quality Assurance (QA) team plays a vital role in making that possible. We're looking for a Quality Assurance Auditor to join our Evansville team and help ensure compliance, integrity, and excellence in every project.
- Purpose-driven work – your expertise ensures the reliability of data that drives life-saving research.
- Growth opportunities – expand your QA knowledge through diverse audits, regulatory exposure, and cross-functional collaboration.
- Supportive culture – be part of a team that values integrity, collaboration, and continuous improvement.
- Local stability + global impact – contribute to a mission-driven company with deep Evansville roots and international reach.What We Offer
- Salary - This is a non-exempt role paying $26.50 - $33.50 / hour and can adjust along with the level of the role to match the person's relevant experience and / or education level. 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.
- Benefits - Medical, dental, and vision effective within 30 days; 401k with employer match effective after 90 days; 23 PTO days + 10 paid holidays annually; overtime opportunities paid at 1.5x rate
- Schedule - Monday - Friday, 7 : 30a - 4p (flexible on hours, and this position may require earlier arrivals to accommodate study activities; advance notice will be provided)
- Location - Mount Vernon, IN (just 5 minutes past USI's campus)What You'll DoAs a QA Auditor, you'll be the bridge between regulatory standards and scientific excellence. Your day-to-day may include :
- Conducting audits of studies, facilities, and records to ensure compliance with protocols, SOPs, and GLP regulations.
- Reviewing protocols, study data, reports, facility documentation, and subcontractor contributions.
- Observing laboratory practices and processes to identify risks and areas for improvement.
- Preparing and delivering audit reports with findings and recommendations.
- Supporting inspections by sponsors and regulatory agencies.
- Providing guidance and training on regulatory topics to colleagues.
- Collaborating with the QA team to continuously strengthen processes and outcomes.What We're Looking For Education / Experience : + B.S. in Chemistry, Life Sciences, or related field, OR + 1–3 years of pharmaceutical auditing experience, OR + 3–5 years of pharmaceutical lab experience with at least 1 year in auditing, OR + Equivalent blend of education and QA / regulatory experience. Skills : + Strong communication and interpersonal skills—you can partner effectively across all levels. + Highly organized with sharp attention to detail. + Familiarity with laboratory procedures and government regulations. + Comfortable using Word, Outlook, Excel, SharePoint, and electronic data systems. + Able to work independently while staying collaborative and solutions-oriented.What to Expect
- Mix of desk-based work and active lab / facility presence.
- Some physical activity, including walking, standing, and light-to-moderate lifting (up to 50 lbs).
- Occasional business travel. This role is a great fit if you're looking to grow your career in quality assurance while contributing to research that truly matters. Apply today and help us drive science forward. #LI-Onsite #LI-OF1
- 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. ### Get In TouchIntroduce 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!
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