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Tango Therapeutics
Boston, MA
Source: Tango Therapeutics careers · View original posting
From Tango Therapeutics's posting. “We” and “our” refer to the employer.
Company Overview
Tango Therapeutics is a biotechnology company dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the treatment of cancer.
Using an approach that starts and ends with patients, Tango leverages the genetic principle of synthetic lethality to discover and develop therapies that take aim at critical targets in cancer.
This includes expanding the universe of precision oncology targets into novel areas such as tumor suppressor gene loss and their contribution to the ability of cancer cells to evade immune cell killing.
The Tango labs and offices are located at
201 Brookline Avenue, in the Fenway area of Boston, Massachusetts.
Summary
This role will report to the Director of Quality and operate across departments, supporting regulated activities and studies. This new role will support CMC development and clinical disposition activities for Tango’s development programs. Tango works in a matrixed, outsourced model where compliance and inspection readiness are key to our programs as we advance through the development cycle.
The Manager, Quality Assurance, will provide GMP QA oversight for Tango’s CMC development programs and clinical supply activities. This role partners cross-functionally with Technical Operations, Regulatory, and external manufacturing partners to ensure compliance with global GMP requirements while supporting the advancement of investigational therapies through clinical development.
Review batch documentation and dispositions materials for use in clinical trials
Lead & manage strategic GMP QA activities associated with Tango CMC development programs
Ensure compliance with regulations related to manufacturing, testing, packaging & distribution of investigational drug products and active pharmaceutical ingredients. Identify compliance gaps and propose solutions
Execute and lead implementation of phase-appropriate quality guidance, review, and approval processes for product development programs across Phases 1–3
Oversee projects independently, identifying, evaluating, and resolving product quality concerns in compliance with GMP requirements
Identify trends related to development compounds, operations, etc.
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
Compensation
$116,000 — $174,000 USD
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