Backed by Third Rock Ventures.
About the role
Seaport Therapeutics is a clinical-stage biopharmaceutical company advancing the development of novel neuropsychiatric medicines in areas of high unmet patient needs. The Company has a proven strategy of advancing clinically validated mechanisms previously held back by limitations that are overcome with its proprietary GlyphTM technology platform.
What they're looking for
- Bachelor's degree in Science or related fields
- 8 – 10 years of experience in the pharmaceutical or biotechnology industry, with significant expertise in Quality or a related function
- Strong knowledge of GMP and regulatory requirements, with hands-on experience managing external CMOs
- Strong organizational, analytical, and problem-solving skills, with the ability to manage multiple priorities in a dynamic environment
- Small molecule drug development experience highly desirable
- Motivated by patient focus and personal commitment to high performance and results
More about this role
Seaport Therapeutics is a clinical-stage biopharmaceutical company advancing the development of novel neuropsychiatric medicines in areas of high unmet patient needs. The Company has a proven strategy of advancing clinically validated mechanisms previously held back by limitations that are overcome with its proprietary GlyphTM technology platform. All the therapeutic candidates in its pipeline of first and best-in-class medicines are based on the Glyph platform, which is uniquely designed to enable oral bioavailability, bypass first-pass metabolism and reduce hepatotoxicity and other side effects. Seaport is led by an experienced team that invented and advanced important neuropsychiatric medicines and are guided by an extensive network of renowned scientists, clinicians and key opinion leaders. For more information, please visit www.seaporttx.com .
Reporting to the Head of Quality, Seaport Therapeutics is seeking an experienced Associate Director, Quality Assurance CMC to manage GMP quality assurance activities supporting clinical development programs, ensuring compliance with Good Manufacturing Practice (GMP), regulatory requirements, and company policies. This role is...
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