Job Description The QC Manager / Group Leader is responsible for leading a team of approximately seven lab technicians in a GMP (Good Manufacturing Practice) environment, working fully onsite at a laboratory in Indianapolis. The primary focus is overseeing routine quality control testing for clinical supplies—ensuring medical packaging such as syringes and vials are safe and do not leak—while keeping operations running smoothly. This leader plans daily work, assigns tasks, manages schedules, and ensures timely completion of all activities. The role includes managing documentation, supporting audit preparation, and ensuring strict adherence to GMP standards. Troubleshooting is generally minor, with the QC Manager / Group Leader providing guidance as needed. Success in this position requires fostering a positive team culture and maintaining strong communication with other departments in a dynamic, fast-paced setting. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/. Skills and Requirements Education & Experience: Bachelor’s degree & 4 years of relevant experience, or Master’s degree & 2 years of relevant experience. Demonstrated experience leading teams in a GMP laboratory environment (leadership does not need to be in identical test types). Laboratory testing experience (No specific type required - PLEASE make sure to document which type) Strong interpersonal skills and professional presence, with the ability to build trust, communicate effectively, and foster a supportive team environment. Proven ability to manage documentation, validations, and method-related reports in compliance with GMP standards. Hands-on experience with container closure integrity (CCI) methods and dye ingress protocols. Background in clinical supplies workflows and sample logistics. Experience preparing for regulatory audits and supporting audit responses. Exposure to validation or method development documentation in QC or packaging contexts.