Quality Control Reports Coordinator

Quality Control Reports Coordinator: This position is responsible for auditing raw data for compliance with Good Laboratory Practices (GLP) data recording regulations, study protocols and appropriate Standard Operating Procedures (SOPs). This position is also responsible for compiling and generating all raw data into a study report with the appropriate tables and appendices

• Read, apply, and maintain adherence to GLP regulations, SOPs, and client protocols
• Demonstrate basic understanding of GLP regulations and their implementation
• Collate and organize raw data records into data books
• Understand purpose and procedures of raw data forms
• Responsible for auditing raw data for consistency, completeness, and accuracy
• Maintain a strong working relationship with the Quality Assurance (QA) Department
• Provide input to management about process improvement
• Provide additional QC data review support as needed
• Work with various personnel to ensure reports are accurate and completed in a timely manner
• Work with Inotiv Evansville Study Directors to implement the needs of each report
• Be familiar with all types of data generated by the lab and be able to incorporate into the final report
• Perform any report function as requested by Study Director or immediate supervisor
• Keep abreast of information relating to government guidelines and specified sponsor requests
• Generate special tables and analysis not performed by computer
• Electronic formatting for individual reports
• Data entry Participate in in-house training programs for the technical staff
• Maintain confidential information

Bachelor’s degree in related science with Quality Assurance/ Quality Control and/or Laboratory Animal Technician experience preferred.

*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.

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, 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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