Manufacturing Associate I

at  Moderna

The Role
In this role, you will be part of a cohesive team responsible for Individualized Neoantigen Therapy (INT) Drug Substance (DS) clinical manufacturing. You will produce GMP mRNA-based medicines, applying new and existing knowledge of bioprocess unit operations and cGMPs to enable technical success with stringent adherence to a Quality System that respects global regulatory expectations. You will operate pilot-scale bioprocessing equipment and interact fluidly with peers and supervisors in Manufacturing, and cross-functionally with Quality Assurance, Digital Support, Manufacturing Sciences and Technology, Quality Control, and Logistical counterparts.
This position is located at Moderna’s GMP Manufacturing site in Norwood, MA. Night shift (12hr Shifts: 6pm-6am).
Here’s What You’ll Do
Practice safe work habits and adhere to Moderna’s safety procedures and guidelines.
Execute manufacturing operations using disposable technologies, automation, and Manufacturing Execution Systems (MES) to produce mRNA.
Demonstrate general knowledge of standard manufacturing practices and equipment.
Strict adherence to current good manufacturing practices, standard operating procedures, and manufacturing documentation.
Establish and follow written procedures for the clear and accurate documentation of equipment operation and process instructions, and of process data.
Monitor process operations to ensure compliance with specifications.
Closely partner with QA peers for rapid disposition of mRNA.
Assist in the investigation of procedural deviations.
Utilize knowledge to improve operational efficiency.
Adhere to gowning procedures and maintain a clean general operating area.
Adhere to documented waste handling procedures to respect environmental regulations.
Additional duties as may be assigned from time to time.
Here’s What You’ll Need (Minimum Qualifications)
Bachelor’s degree in Biology, Chemistry, Chemical Engineering, Biomechanical Engineering, Bioengineering, Biomedical Engineering, Biochemistry, or related field.
Associates with 2+ years related experience or 4+ years of related GMP experience.
Here’s What You’ll Bring to the Table (Preferred Qualifications)
Work in a complex, fast-paced manufacturing environment and rapidly adapt to changes.
Demonstrate consistent punctuality and recognize its importance in our operations.
Document and communicate technical and operational observations clearly and efficiently.
Exhibit honesty and uphold high ethical standards. Demonstrate unwavering integrity in all professional matters.
Maintain a positive attitude at all times, especially when challenges arise.
Participate actively and respectfully in team discussions and meetings.
Cultivate a positive work environment by consistently demonstrating a supportive and team-oriented attitude.
Engage with all team members respectfully. Acknowledge and appreciate their value.
Accomplish goals by working together and respecting others’ viewpoints. Be one team.
Deliver on the promise of mRNA technology to transform lives. Be visionary.
Seek to challenge and improve upon the status quo. Be innovative.
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 options
Flexible Spending Accounts for medical expenses and dependent care expenses
Lifestyle Spending Account funds to help you engage in personal enrichment and self-care activities
Family care benefits, including subsidized back-up care options and on-demand tutoring
Free premium access to fitness, nutrition, and mindfulness classes
Exclusive preferred pricing on Peloton fitness equipment
Adoption and family-planning benefits
Dedicated care coordination support for our LGBTQ+ community

Please refer the Job description for details