Engineer II, Drug Product, Manufacturing… at Moderna · Norwood

Summary: Moderna is a pioneering company revolutionizing medicine through mRNA technology. The Engineer II role focuses on supporting product labeling, packaging, and storage processes to ensure high-quality mRNA medicines reach patients. Responsibilities: - Supporting day-to-day technical activities related to both automated and manual label and packaging equipment, as well as the storage conditions of finished drug product - Participating in execution and monitoring of packaging and storage processes to ensure optimal performance - Drafting and contributing to SOPs related to labeling and packaging workflows, ensuring they meet evolving GMP and regulatory expectations - Supporting deviation investigations and implementing corrective and preventive actions (CAPAs) - Assisting with updates to batch records and controlled documentation within the GMP framework - Participating in internal and external audit activities as a subject matter expert in label and packaging - Collaborating directly with Process Experts and Technicians to ensure consistent process performance - Acting as a liaison between Operations and the Quality organization to enable compliant, high-quality product handling - Engaging in continuous improvement initiatives under the guidance of senior team members - Ensuring strict adherence to Moderna’s GMP standards while supporting operational readiness and scalability Required Qualifications: - Bachelor's or Master's degree in Chemical Engineering, Biochemical Engineering, Biotechnology, or related field - A minimum of 1-3 years of experience in the biotech or pharmaceutical industry, with a focus on drug formulation, filling processes and label and packaging - Strong understanding of GMP regulations and guidelines - Proven ability to troubleshoot issues related automated systems - Strong written and verbal communication skills - Candidates must already hold work authorization in US and be able to maintain that status without the need for future sponsorship Required Skills: GMP regulations, Drug formulation, Label, packaging Important Skills: Troubleshooting automated systems, SOP writing Nice-to-Have Skills: Continuous improvement, communication skills Benefits: 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