Quality Assurance Specialist

Quality Assurance Specialist

Isotopia is a global biotech company manufacturing key ingredients for pharmaceutical cancer drugs. At our US headquarters in Indianapolis, we will be next door to our key customers, delivering our products just in time, each day, every day. We are seeking a highly motivated and detail-oriented Quality Assurance Specialist to join our dynamic team. You will play a crucial role in ensuring the safe and efficient production of our products. You will be part of a family and a team, dedicated to our mission to deliver on our covenant with our customers.

Responsibilities:

• Creation, implementation and support of a comprehensive QMS (Quality Management System).
• Participate in the qualification of key suppliers, including executing internal and external audits and assessments.
• Creation and implementation of processes which support manufacturing of active drug substance, such as issuance of batch records and test records, raw material release, batch record review, and finished drug product release.
• Creation and management of site training and development programs, including GMP and GDP training.
• Support of critical manufacturing investigations, including out of specification results and deviations in the manufacturing process.
• Support the preparation and submission of regulatory filings, agency responses, and supplements to include FDA deficiency resolution, annual reporting and other correspondence between Isotopia and regulatory agencies (Nuclear Regulatory Commission, Food and Drug Administration, European Union, etc.).
• Execution of other tasks as needed to support ongoing tasks and projects critical to the success of the site.