Senior Scientist, Sterile Oligonucleotide Formulations

Stoke Therapeutics

Bedford (MA)

Vor Ort

USD 160.000 - 173.000

Vollzeit

Vor 4 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Annual bonus
Equity participation
Medical, dental, vision
401K with company match
Unlimited vacation

Zusammenfassung

Stoke Therapeutics in Bedford, MA is seeking a Senior Scientist, Sterile oligonucleotide drug product development to help drive formulation development and process scale-up for investigational medicines. The role focuses on translating R&D to compliant manufacturing with contract facilities.

You will apply robust scientific methods, lead experiments, and contribute to regulatory documentation while collaborating with CMOs. Office-based, with travel required.

Qualifikationen

  • PhD in Bio/Chemical Engineering, Pharmaceutical Sciences, or related field with 4+ years of industry experience; MSc with 6+ years; or BSc with 10+ years.
  • One or more years of experience in oligonucleotide or mRNA sterile drug product development.

Aufgaben

  • Develop oligonucleotide prototype formulations in-house and scale up processes to manufacturing at contract facilities.
  • Apply DOE and perform characterization using DSC, UV/Vis, HPLC, LC-MS, viscometry, and particle sizing.
  • Lead experiments, analyze data, and document results for regulatory filings and MBR/MBR reviews.
  • Collaborate with CMOs, select equipment, and support manufacturing operations to mitigate risks.
  • Travel 5-10% as needed.

Kenntnisse

Independent leadership
Problem solving

Ausbildung

PhD in related field
Advanced degree options (MSc/BSc)

Tools

JMP
MasterControl
Veeva
Prism

Jobbeschreibung

Stoke Therapeutics in Bedford, MA is seeking a Senior Scientist, Sterile oligonucleotide drug product development to help drive formulation development and process scale-up for investigational medicines. The role focuses on translating R&D to compliant manufacturing with contract facilities.

You will apply robust scientific methods, lead experiments, and contribute to regulatory documentation while collaborating with CMOs. Office-based, with travel required.

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