Engineer II, Drug Product Development
Norwood, MN - USA
Job Summary
The Role:
We are seeking a highly skilled and motivated Engineer II in Drug Product Development to work in a team developing Modernas 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. The applicant should have 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.
Heres What Youll Do:
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.
Heres What Youll Need (basic qualifications):
Education Qualifications - Masters or Bachelors Degree in on one of the following fields: Mechanical Packaging or Chemical Engineering Pharmaceutical Sciences or any related or sub-disciplines of the above.
Relevant Experience: 0 2 years post Masters Degree or at least 2 years post Bachelors Degree.
Exceptional laboratory skills with ability to work efficiently and productively in a highly dynamic environment
Knowledge of statistical design of experiments (DoE) and analysi
This position is site-based requiring you to be at Modernas site full-time. This position is not eligible for remote work.
Heres What Youll Bring to the Table (preferred):
Preferred: Experience in BioPharma BioPharmaceutical Pharmaceutical or Biotechnology industry
Preferred: Knowledge of GMP compliance.
Pay & Benefits
At Moderna we believe that when you feel your best you can do your best work. Thats why our US benefits and global well-being resources are designed to support youat work at home and everywhere in between.
Best-in-class healthcare coverage plus voluntary benefit programs to support your unique needs
A holistic approach to well-being with access to 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
Location-specific perks and extras
About Moderna
Since our founding in 2010 we have aspired to build the leading mRNA technology platform the infrastructure to reimagine how medicines are created and delivered and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.
By living our mission values and mindsets every day our people are the driving force behind our scientific progress and our culture. Together we are creating a culture of belonging and building an organization that cares deeply for our patients our employees the environment and our communities.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer a Fast Company Best Workplace for Innovators and a Great Place to Work in the U.S.
If you want to make a difference and join a team that is changing the future of medicine we invite you to visit to learn more about our current opportunities.
Our Working Model
As we build our company we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation teamwork and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn contribute and make a meaningful impact.
Moderna is a smoke-free alcohol-free and drug-free work environment.
Equal Opportunities
Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a persons 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 is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day please apply!
Moderna is an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories consistent with legal requirements.
Accommodations
Were focused on attracting retaining developing and advancing our employees. By cultivating a workplace that values diverse experiences backgrounds and ideas we create an environment where every employee can contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations team at .
Export Control Notice This position may involve access to technology or data that is subject to U.S. export control laws including the Export Administration Regulations (EAR). As such employment is contingent upon the applicants ability to access export-controlled information in accordance with U.S. law. Due to the nature of the work and regulatory requirements only individuals who qualify as U.S. persons (citizens permanent residents asylees or refugees) are eligible for this position. For this role Moderna is unable to sponsor non-U.S. persons to apply for an export control license. #LI-TR2-
Required Experience:
IC
About Company
Learn how we’re changing the world of medicine. Discover career opportunities, our product pipeline, and browse media resources. Meet Moderna.