Engineer II, Drug Product Development
Listed on 2026-06-18
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Engineering
Biomedical Engineer, Research Scientist, Quality Engineering, Process Engineer
The Role
We are seeking a highly skilled and motivated Engineer II in Drug Product Development to work in a team developing Moderna’s device combination products that enable clinical and future commercial supply. The primary role for this position will be to support drug product development activities including: device development, combination product development and packaging development. Applicants should have relevant device engineering related experience in the pharmaceutical space and exceptional ability to plan, execute and report, to communicate and collaborate, and requires strong attention to detail while working in a fast-paced, interdisciplinary environment.
Responsibilities- Plan, organize and execute experiments to support combination product/device development – prepare study protocols and summarize the development results with presentations and study reports.
- Contribute to combination product technical documentation including design history file documents, design input requirements, test plans/protocol/reports, engineering assessments, and design outputs.
- Perform required risk assessments, propose mitigation strategies, and document approaches through appropriate risk management systems.
- Communicate and collaborate with various groups such as analytical development to execute experiments and compile data.
- Maintain an up-to-date ELN with good documentation practices.
- Closely collaborate with multiple groups to generate innovative solutions to challenging device problems.
- Education:
Masters or Bachelor’s Degree in Mechanical, Packaging or Chemical Engineering, Pharmaceutical Sciences, or related sub-disciplines. - Relevant
Experience:
0 – 2 years post Master’s Degree or at least 2 years post Bachelor’s Degree. - Exceptional laboratory skills with ability to work efficiently and productively in a highly dynamic environment.
- Knowledge of statistical design of experiments (DoE) and analysis.
- Experience in Bio Pharma, Bio Pharmaceutical, Pharmaceutical, or Biotechnology industry.
- Knowledge of GMP compliance.
- Best‑in‑class healthcare coverage, plus voluntary benefit programs to support your unique needs.
- Health and wellness resources including fitness, mindfulness, and mental health support.
- Family planning benefits, including fertility, adoption, and surrogacy support.
- Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year‑end shutdown.
- Savings and investment opportunities to help you plan for the future.
This position is site‑based, requiring you to be at Moderna’s site full time and is not eligible for remote work. Salary range: $74,000.00 - $.
Work EnvironmentModerna champions a smoke‑free, alcohol‑free, and drug‑free work environment.
EEO StatementModerna is committed to equal employment opportunity and non‑discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law.
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