10 дней назад
Engineer II, Drug Product Development
74 000 - 118 400$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Engineer II, Drug Product Development (Pharmaceutical Sciences/Biotechnology): Developing sterile drug product processes and products for clinical and future commercial supply with an accent on formulation, aseptic fill/finish operations, scale-up, and container compatibility. Focus on designing experiments, characterizing processing and stability, supporting technology transfer, and solving manufacturing process challenges.
Location: Norwood, Massachusetts, United States; full-time, on-site role with up to 20% travel.
Salary: $74,000–$118,400 per year, with potential bonus, incentive compensation, or equity eligibility.
Company
develops mRNA technology and medicines for clinical and commercial use.
What you will do
- Develop sterile drug product processes, formulations, and aseptic fill/finish unit operations for clinical and future commercial supply.
- Conduct scale-up and technology-transfer studies covering freeze/thaw, mixing, filling, filtration, lyophilization, transport, and stability.
- Develop protocols to evaluate compatibility with processing materials, container-closure components, and sterilization processes.
- Plan and execute experiments using design of experiments where appropriate, then prepare protocols, presentations, and study reports.
- Perform characterization activities including opacity testing, microscopy, and particle sizing, while supporting troubleshooting and investigations.
- Collaborate with analytical development, pilot operations, manufacturing, and other interdisciplinary groups to solve formulation and process challenges.
Requirements
- Master’s or bachelor’s degree in chemical engineering, biochemical or biomedical engineering, pharmaceutical sciences, materials science, or a related discipline.
- 0–2 years of relevant experience after a master’s degree or at least 2 years after a bachelor’s degree.
- Strong laboratory skills and the ability to work efficiently in a dynamic environment.
- Knowledge of statistical design of experiments and data analysis.
- Ability to work on-site in Norwood, Massachusetts, United States.
- Access to export-controlled information may require U.S. person status or an export license.
Nice to have
- Experience in the biopharma, biopharmaceutical, pharmaceutical, or biotechnology industry.
- Knowledge of GMP compliance.
- Knowledge of nucleic acid chemistry and biology.
Culture & Benefits
- Healthcare coverage and voluntary benefits.
- Fitness, mindfulness, and mental health resources.
- Family planning support, including fertility, adoption, and surrogacy benefits.
- Paid vacation, volunteer days, sabbatical, global recharge days, and discretionary year-end shutdown.
- Savings and investment programs, plus location-specific benefits.
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