Encoded Therapeutics
Encoded Therapeutics Benefits Overview
Compensation + Benefits
Offers 401(K)
Offers life insurance
Offers disability insurance
Offers accidental death & dismemberment insurance
Offers company equity
Offers performance bonuses
Offers dental insurance
Offers health insurance
Offers Flexible Spending Account (FSA)
Offers vision insurance
Offers generous parental leave
Work-Life Balance + Wellbeing
Offers company-sponsored outings
Offers an Employee Assistance Program (EAP)
Offers generous PTO
Provides paid sick days
Provides paid holidays
Provides bereavement leave
Career Growth + Development
Provides customized development tracks
Company Culture
Office is pet friendly
Provides free snacks and drinks
Recently posted jobs
Biotech
Provides external quality assurance oversight for CDMOs and analytical laboratories supporting clinical and commercial gene therapy supplies. Reviews GMP documentation, batch records, specifications, testing protocols, deviations, CAPAs, and change controls. Authors quality procedures, monitors quality metrics, guides cross-functional compliance decisions, manages suppliers, and supports audits, regulatory inspections, technology transfers, and commercial readiness.
Biotech
Designs and analyzes small-scale upstream process studies for AAV and plasmid manufacturing. Supports preclinical and clinical manufacturing across upstream, downstream, fill-finish, and drug-device processes; facilitates technology transfers to internal and external GMP sites; provides on-site manufacturing support; and develops tools for technology-transfer workflows. Requires expertise in cell culture, single-use bioreactors, cGMP, process sciences, and preferably gene therapy processes.
Biotech
Lead Site Quality Assurance for a clinical manufacturing facility, overseeing CGMP compliance, quality operations, batch disposition, investigations, CAPA, change control, validation, regulatory inspections, supply chain quality, environmental monitoring, and data integrity. Build and mentor the local QA team, provide quality oversight for AAV and gene therapy manufacturing, support regulatory filings, and drive risk-based decisions and continuous improvement.
