2 дня назад
Specialist, Analytical Technical Operations (mRNA/LNP)
74 000 - 118 400$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Specialist, Analytical Technical Operations (mRNA/LNP): Coordinating analytical testing, stability studies, data management, and digital operations for mRNA and LNP drug candidates with an accent on CMC development, laboratory efficiency, and data integrity. Focus on integrating laboratory systems, trending analytical data, coordinating cross-functional timelines, and improving automated workflows for regulated development programs.
Location: Site-based in Norwood, Massachusetts; full-time on-site attendance required. This position is not eligible for remote work. Only U.S. persons are eligible due to U.S. export control requirements.
Salary: $74,000–$118,400 per year, plus potential annual discretionary bonus, incentive compensation, or equity award.
Company
develops mRNA-based therapeutics and vaccines using mRNA science, delivery technology, and manufacturing capabilities.
What you will do
- Coordinate analytical testing schedules across CMC Development programs, laboratory capacity, digital systems, and program priorities.
- Support the authoring, execution, and maintenance of stability protocols and studies for mRNA and LNP drug candidates.
- Compile, review, trend, and summarize analytical data; perform peer reviews and prepare technical data packages.
- Coordinate multiple program timelines, testing milestones, study deliverables, and reporting commitments.
- Support forecasting, sample management, testing strategies, and development program planning with cross-functional teams.
- Improve laboratory efficiency through digital tools, automated workflows, system integration, and data management processes.
Requirements
- Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Biology, Chemical Engineering, or a related scientific discipline.
- 3–6 years of experience in biotechnology, pharmaceuticals, analytical development, technical operations, or CMC Development.
- Experience with stability studies, analytical testing programs, or laboratory operations in a regulated environment.
- Experience with LabVantage, Benchling, or similar LIMS, ELN, or laboratory data management systems.
- Strong organizational, analytical, problem-solving, communication, and prioritization skills.
- Must work full-time at ’s site in Norwood, Massachusetts and qualify as a U.S. person under applicable export control requirements.
Nice to have
- Experience with mRNA, LNP, biologics, or other advanced therapeutic modalities.
- Familiarity with CMC Development, stability programs, and regulatory expectations.
- Experience with process improvement, workflow optimization, automation, digital transformation, or cross-functional project coordination.
Culture & Benefits
- In-person culture supported by a 70/30 work model with emphasis on office collaboration, teamwork, and mentorship.
- Healthcare and voluntary benefit programs.
- Fitness, mindfulness, and mental health resources.
- Family planning support, including fertility, adoption, and surrogacy benefits.
- Paid time off including vacation, volunteer days, sabbatical, global recharge days, and year-end shutdown.
- Savings and investment programs.
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