10 дней назад
Director, Analytical Development (mRNA)
167 000 - 300 700$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Director, Analytical Development (mRNA): Leading next-generation analytical methods and technologies across Moderna’s Quality Control network with an accent on method innovation, lifecycle adoption, automation, and regulatory readiness. Focus on translating emerging analytical science into scalable methods, guiding technology transfer and validation, and building cross-functional capabilities for mRNA and advanced therapeutic modalities.
Location: 100% onsite in Norwood, Massachusetts, United States. Due to U.S. export control requirements, only U.S. persons are eligible.
Salary: $167,000–$300,700 per year, with potential annual bonus, incentive compensation, or equity award.
Company
develops mRNA medicines and advanced therapeutic technologies through its mRNA platform.
What you will do
- Lead the Innovative Technology and Methodology capability within Analytical Development and define the strategy and roadmap for next-generation analytical methods.
- Build an end-to-end innovation pipeline from unmet analytical needs and proof of concept through development, validation, transfer, implementation, and lifecycle adoption.
- Drive modernization, replacement, simplification, consolidation, and harmonization of analytical methods across the Quality Control network.
- Partner with Analytical Sciences, QC, AST, Quality, Regulatory, Digital, Automation, and external organizations to implement scalable analytical technologies.
- Advance automation-, digital-, and data-enabled workflows that improve robustness, throughput, data integrity, and review efficiency.
- Develop scientific talent and establish success measures for analytical innovation, including method performance, turnaround time, cost, and network adoption.
Requirements
- Ph.D. in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering, Bioengineering, or a related field with 12+ years of relevant industry experience; alternatively, an M.S. or B.S. with 18+ years of relevant experience.
- Extensive experience in analytical development, analytical technology, or pharmaceutical sciences for biologics, vaccines, mRNA, or other advanced therapeutic modalities.
- Experience defining analytical innovation strategies and moving technologies from proof of concept through implementation, transfer, validation, change control, and adoption.
- Strong knowledge of analytical procedure lifecycle principles, GMP, data integrity, global regulatory expectations, ICH Q14, and Q2(R2).
- Demonstrated leadership of complex matrixed initiatives and scientific talent across Analytical Development, QC, Manufacturing, Quality, Regulatory, Digital, and external partners.
- Must be a U.S. person eligible to access export-controlled information; cannot sponsor non-U.S. persons for an export control license.
Nice to have
- Experience with analytical automation, high-throughput workflows, digital integration, advanced data analysis, or AI/ML-enabled analytical applications.
- Experience with nucleic acids, lipid nanoparticles, vaccines, biologics, advanced characterization, or other advanced modalities.
- Experience collaborating with technology vendors, academic groups, consortia, CROs, and CDMOs.
Culture & Benefits
- In-person work model with direct collaboration, mentorship, and hands-on partnership at the site.
- Healthcare and voluntary benefit programs, fitness and mental health support, and family planning benefits.
- Paid vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown.
- Savings and investment programs, plus location-specific perks and extras.
- Smoke-free, alcohol-free, and drug-free work environment.
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