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Engineer II, Manufacturing Science and Technology
2 months ago
The Role
In this role, you will be part of Modernas Manufacturing Science and Technology team responsible for process implementation, technical support, and person-in-plant coverage to ensure the robust End-to-End production of our new mRNA Individualized Neoantigen Therapies (INT). The individual will work collaboratively with cross functional stakeholders such as Technical Development, Manufacturing, Regulatory, and Quality, to ensure all technical aspects of production are successfully executed. This will be a 1st shift role and the individual will be working a Sunday through Wednesday schedule from 6:00am until 4:00pm.
Heres What Youll Do
Provide expertise in bioprocessing unit operations and cGMP manufacturing, responsible for technical support, change control, safety observations, manufacturing investigations, and person-in-plant coverage for the INT process. Support process training for GMP operations and development of process understanding and expertise. Train and assist the manufacturing team in operational excellence projects driven by 5S, Lean Six Sigma, and similar programs. Lead/participate in cross functional technical process support and investigation teams. Partner with Technical Development, Manufacturing, and Quality to enable and sustain cGMP processes. Be the technical lead supporting cGMP manufacturing activities. Be the subject matter expert for plasmid, drug substance, and lipid nanoparticle processes for the INT process. This includes troubleshooting process and equipment issues. Author deviation/investigation reports, technical reports, and manage technical CAPA/change controls. Establish and maintain process performance trending / metrics using digital information and statistical analysis tools. MS&T will be providing weekend coverage for Manufacturing and as part of the team you will need to be flexible to work a weekend day on a rotational basis. Additional duties as may be assigned from time to time. Heres What Youll Need (Basic Qualifications) Biochemical engineer, Chemical engineer, Biochemistry or Biology background. BS with 3 to 5 years of experience or MS with 1 to 3 years experience in a pharmaceutical or biotechnology company. Heres What Youll Bring to the Table (Preferred Qualifications) Demonstrated knowledge of cGMPs and experience providing technical support in a cGMP manufacturing environment. Demonstrated expertise bioprocessing including fermentation and purification of protein and/or nucleic acids. Expertise in at least one of the following areas: chromatography, membrane separations, fermentation, enzymatic reactions, and formulation. Technical agility. The capability to manage diverse technical areas. Ability to collaborate effectively in a dynamic, cross-functional matrix environment. Preferred: Expertise in molecular biology Preferred: Experience in biologics process development and scale up / scale down. Preferred: Experience with single use bioprocessing technologies. Preferred: Proven track record leading and managing cross functional teams. Preferred: Knowledge of digital cGMP tools. For example: SAP, OSI PI, MES (eBR), Unicorn, eQMS A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative. This position is site-based, requiring you to be at Modernas site full-time. This position is not eligible for remote work. Moderna is pleased to provide you and your family with a comprehensive and innovative suite of benefits, including:Highly competitive and inclusive medical, dental and vision coverage optionsFlexible Spending Accounts for medical expenses and dependent care expensesLifestyle Spending Account funds to help you engage in personal enrichment and self-care activitiesFamily care benefits, including subsidized back-up care options and on-demand tutoringFree premium access to fitness, nutrition, and mindfulness classesExclusive preferred pricing on Peloton fitness equipmentAdoption and family-planning benefitsDedicated care coordination support for our LGBTQ+ communityGenerous paid time off, including:Vacation, sick time and holidays
Volunteer time to participate within your community
Discretionary year-end shutdown
Paid sabbatical after 5 years; every 3 years thereafterGenerous Paid Leave offerings, including 18 weeks of 100% paid parental leave for all new parents 401k match and Financial Planning toolsModerna-paid Life, LTD and STD insurance coverages, as well as voluntary benefit optionsComplimentary concierge service including home services research, travel booking, and entertainment requestsFree parking or subsidized commuter passesLocation-specific perks and extras About Moderna Since our founding in 2010, we have aspired to build the leading mRNA technology platform, theinfrastructure 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 peopleare 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. 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.
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.
Moderna is a smoke-free, alcohol-free and drug-free work environment.
Moderna 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 proud to be an equal opportunity workplace and is an affirmative action employer.
Moderna 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. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. Were focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to 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 (EEO/AAP Employer)
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