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Director, Quality Assurance
The Director, Quality Assurance will be responsible for the GMP audit and compliance functions of the Quality Assurance Department, including QA documentation, and support for GLP and GCP operations. This position will report directly to the President.
Clinical Research Associate
The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP and all applicable regulatory requirements.
Manager, Clinical Supply Chain and Packaging
The Manager of Clinical Supply Chain and Packaging will be responsible for clinical labeling, packaging and distribution as well as for planning and implementing activities related to the timeline, cost-effective procurement, inventory and quality control of reference standard and production intermediates.
Director Regulatory Affairs
The Director, Regulatory Affairs is responsible for leading and reviewing the company’s regulatory strategy and gaining an understanding of the regulatory requirements for approval, to make recommendations to the development team. He/she supervises the preparation of all regulatory agency submissions, compliance and communications.
Associate Director, Drug Product Development
The Associate Director, Drug Product Development will play a pivotal role in advancing our therapeutic innovations through the formulation and development of drug products from the pre-IND to the clinical stages. They will be responsible for overseeing the design, optimization, and validation of drug product processes while ensuring alignment with regulatory standards and company objectives.
Senior Scientist, Drug Substance Manufacturing
The Senior Scientist, Drug Substance Manufacturing will be responsible for the manufacturing of drug substances at external providers. They will oversee the technical aspects of drug substance route scouting, process development and manufacturing activities including process transfer, scale-up, registration batch manufacture, validation, launch, on-going manufacturing support and process improvements.
We want leaders who will champion programs and change lives.
Thryv Therapeutics is proud to be an equal opportunity workplace and an affirmative action employer.