Manufacturing Associate I, INT
Moderna
Summary
As a Manufacturing Associate I, you will be a key member of a cohesive team responsible for the production of GMP mRNA-based medicines. Your role will involve operating bioprocessing equipment, adhering to cGMP guidelines, and collaborating with various departments to ensure the success of manufacturing processes. This position requires working 12-hour shifts.
Job description
The Role
As a Manufacturing Associate I, you will be a key member of a cohesive team responsible for the production of GMP mRNA-based medicines. Your role will involve operating bioprocessing equipment, adhering to cGMP guidelines, and collaborating with various departments to ensure the success of manufacturing processes. This position requires working 12-hour shifts.
Here's What You'll Do
- Practice safe work habits and adhere to safety procedures and guidelines.
- Execute manufacturing operations using disposable technologies, automation, and Manufacturing Execution Systems (MES).
- Demonstrate general knowledge of standard manufacturing practices and equipment.
- Maintain strict adherence to current good manufacturing practices (cGMP), standard operating procedures (SOPs), and manufacturing documentation.
- Establish and follow written procedures for clear and accurate documentation of equipment operation, process instructions, and process data.
- Monitor process operations to ensure compliance with specifications.
- Partner with QA peers for rapid disposition of mRNA.
- Assist in the investigation of procedural deviations and utilize knowledge to improve operational efficiency.
- Adhere to gowning procedures and maintain a clean general operating area.
- Follow documented waste handling procedures to comply with environmental regulations.
Here's What You'll Need (Basic Qualifications)
- Education: Degree
- Experience: 0-3 years relevant experience
- Specific Certifications or Training: None
- Other Quantifiable Preference: Experience in a GMP environment preferred.
Requirements
- Degree
- 0-3 years relevant experience
- Experience in a GMP environment preferred
- Ability to work 12-hour shifts
- Must qualify as a U.S. person (citizen, permanent resident, asylee, or refugee)
Benefits
- Healthcare
- Fitness support
- Mindfulness support
- Mental health support
- Family planning benefits
- Fertility support
- Adoption support
- Surrogacy support
- Paid time off
- Vacation
- Volunteer days
- Sabbatical
- Global recharge days
- Year-end shutdown
- Savings and investments
Company overview
Moderna, Inc. is a pioneering American biotechnology and pharmaceutical company headquartered in Cambridge, Massachusetts, that has revolutionized the field of medicine through its groundbreaking messenger RNA (mRNA) technology. Founded in 2010, the company has established itself as a global leader in RNA therapeutics, primarily focusing on mRNA vaccines and treatments. Moderna's innovative platform uses mRNA to provide cellular instructions for producing proteins that trigger immune responses, creating a new category of medicines with significant potential to improve patient outcomes across various therapeutic areas. The company gained worldwide recognition during the COVID-19 pandemic for developing one of the earliest and most effective mRNA vaccines, which demonstrated the transformative potential of its technology platform. Beyond infectious diseases, Moderna is advancing a diverse pipeline of 44 treatment and vaccine candidates across infectious diseases, immuno-oncology, rare diseases, cardiovascular diseases, and autoimmune conditions. With approximately 5,800 employees and a strong commitment to scientific innovation, Moderna continues to expand its manufacturing capabilities and research initiatives to deliver the greatest possible impact through mRNA medicines.