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Manager, Manufacturing, INT

2 months ago


Norwood, Massachusetts, United States Moderna, Inc. Full time

The Role

In this role, you will oversee the production of clinical drugs in compliance with cGMP guidelines. This hands-on management role is essential for leading a team tasked with producing high-quality mRNA-based medicines for clinical trials. The successful candidate will manage operations effectively, ensuring adherence to safety, quality, and regulatory standards while driving team performance and efficiency. This is a night shift position on a rotating schedule.

Heres What Youll Do Develop and manage operational goals, ensuring objectives are met efficiently. Monitor operations to ensure the safe and timely completion of manufacturing activities. Act as the primary point of contact for technical and compliance issues, facilitating resolution with QA, QC, and Regulatory departments. Ensure compliance with all aspects of GMP, including facilities, SOPs, validation protocols, training, reports, and records. Oversee the hiring, training, development, and retention of manufacturing staff. Maintain a thorough knowledge of cGMPs and FDA guidelines to ensure all manufacturing processes meet regulatory standards. Serve as a subject matter expert on chromatography systems, TFF systems, and single-use process materials. Foster a culture of continuous improvement and operational excellence within the team. Liaise with other company departments to support overall company objectives and ensure smooth manufacturing operations. Additional duties as may be assigned from time to time Heres What Youll Need (Basic Qualifications) Bachelors degree in Science or Engineering relevant to biotechnology preferred. Minimum of 5 years in a biotechnology manufacturing, quality, or development environment. 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 Qualifications) In-depth knowledge of chromatography and TFF systems; additional training in GMP compliance and regulatory standards preferred. 7 years of professional cGMP experience in the biotech, diagnostic, therapeutic, or pharmaceutical industry is highly desirable. Excellent communication skills. Strong leadership, collaboration, and team building skills. Skill in conflict resolution and crucial conversations (within the team and between functions). Technical writing skills and proficient in investigations and root cause analysis. Proven ability to assess risk and collaborate with support groups to develop suitable action plans and minimize potential impact. A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.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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