Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Product facility in Research Triangle Park (RTP). These teams are the backbone of our operations – each playing a critical role in delivering our therapies to the patients who need them. Our teams are organized by the steps in the biomanufacturing process that they operate in; including – Parenteral Filling M - As perform these critical steps in a clean environment governed by Current Good Manufacturing Practices (cGMP). What You’ll Do. Execute daily manufacturing activities, to include operating process equipment and executing validation protocols according to cGMP Standard Operating Procedures (SOPs)Document and record all cGMP data & information (including deviations) for processing steps and equipment activities. Create and revise key documentation like batch records, SL - Rs, and equipment logbooks. Assist in conducting in-process sampling and sampling analysis (p. H, Conductivity, Protein Concentration, Osmolarity, Cell Counts, etc.)Help maintain a clean and safe work environment, always focusing on audit readiness of process areas. Be a team player and leader; always showing up to contribute your energy and focus. Actively participate and lead in training and development initiatives, both for personal growth and for that of your team members. Who You Are. You are someone with a deep passion for doing work that furthers a mission to save lives. Biomanufacturing is complex, so you have a high degree of demonstrated learning agility and love a fast-paced work environment where everything you do is incredibly impactful. Requirements. Bachelor’s Degree (STEM preferred) and at least 2 years of directly transferrable experience OR - Bio. Work Certificate or Associate’s Degree at least 2.5 year of directly transferrable experience OR - High School Diploma (or equivalent) plus at least 3 years of direct and/or military experience Job Level: Entry Level.