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About Us…
Obsidian Therapeutics is expanding the reach of TIL therapy. We are pioneering engineered tumor infiltrating lymphocyte (TIL) therapies to deliver transformative outcomes for patients suffering from solid tumor malignancies. Obsidian’s programs apply our cytoDRiVE® platform technology to express regulated therapeutic proteins to enhance anti-tumor activity. We’re currently investigating our lead program OBX-115 and enrolling patients in an ongoing clinical trial in advanced or metastatic melanoma.
We’re proud of our diverse talented team and committed to cultivating an environment where each person feels a strong sense of belonging and is supported to continuously learn and contribute their best work. Our research team is based in the heart of Cambridge, MA, and our Technical Development, Manufacturing & Quality team is based in our facility in Bedford, MA. Obsidianites enjoy a highly collaborative culture, competitive salary and benefits, and potential for ownership through stock options.
On April 3, 2024, we announced closure of a significantly oversubscribed $160.5 million Series C financing with a top-tier syndicate of life science investors led by new investor, Wellington Management. Proceeds from the financing will advance Obsidian’s lead program in its ongoing trials. We’re focused on enrolling patients and reaching key clinical and regulatory milestones, as well as manufacturing scale-up ahead of pivotal trial readiness.
Our Opportunity…
We’re seeking a visionary and hands-on leader for this newly created position. This position is responsible for oversight of all GXP operations inclusive of leading Clinical Quality, Quality Assurance, Quality Control, Quality Systems, Quality Assurance Validation, Quality Risk Management and Quality Compliance. The charter is to partner across the organization to define and drive a holistic Quality strategy and roadmap to enable success from clinical development through commercialization and cultivate a culture of quality while ensuring overall GxP compliance.
The ideal candidate must bring significant leadership experience in building phase appropriate Quality operations including organization capabilities and quality management systems in small to medium sized biotech companies (including cell- or gene-therapy). Critical success factors include well-rounded GXP experience, success in developing and leading robust Quality operations, developing and motivating high performing teams, and overseeing an externalized GMP environment.
This role reports to our Chief Technical Officer (with a dotted line to the CEO) and is based in our Bedford MA location (hybrid).
You Will…
You Bring…
Core Qualifications
Obsidian is proud to be an equal opportunity employer, cultivating a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status or any other applicable legally protected characteristics.
Full Time
Durable Manufacturing
$243k-328k (estimate)
05/26/2024
07/25/2024
obsidiantx.com
CAMBRIDGE, MA
<25
2015
Private
PAUL K WOTTON
<$5M
Durable Manufacturing
Obsidian Therapeutics is a biotechnology company that discovers and develops cell and gene therapies for the treatment of cancer.