**Downstream Manufacturing Scientist II** Manufacturing Middlesex County, NJ, US + Added - 22/01/2025 Apply for Job We are currently hiring for a Downstream Manufacturing Scientist to join a dynamic and growing biopharmaceutical company. If you are passionate about working in the biotechnology field and have experience in manufacturing processes, we want to hear from you! **Shift:** **Second Shift (2 pm -10pm)** **Location:** Middlesex County, NJ **Pay:** 80-100k Salary **Essential Duties & Responsibilities** + Perform downstream processing at various scales in a cGMP environment, including column packing, process troubleshooting, and data analysis. + Provide technical guidance in the execution and development of purification processes. + Utilize systems to collect and analyze operational data and make real-time adjustments to products, instruments, or equipment. + Ensure timely execution of engineering and clinical batches. + Develop equipment operating specifications and enhance manufacturing techniques. + Collaborate with other teams and external vendors to address technical challenges and maintain production equipment. + Follow GMP guidelines in the manufacturing area and lead efforts to uphold environmental health and safety policies. + Oversee investigations and corrective actions for issues identified during batch execution. + Perform additional tasks as assigned. + Comply with all company policies and operational standards. **Requirements** **Education and Experience** + Bachelor’s or Master’s degree in chemical, biological, or biochemical sciences with 4-5 years of relevant experience in the biopharmaceutical industry. + Experience working in GMP and aseptic manufacturing environments. + Proficiency in operating systems like AKTA Process skids (or similar) and familiarity with single-use manufacturing consumables, including bags, tube sets, columns, and process manifolds. + Knowledge and experience in executing engineering and clinical batches, as well as familiarity with GMP documentation. **Special Skills** + Ability to collaborate with team members and work independently; strong interpersonal skills. + Excellent verbal and written communication skills; strong organizational skills and attention to detail. + Basic computer proficiency, including knowledge of Word, Excel, and spreadsheets. + Expertise in GMP batch manufacturing and packaging documentation, including auditing and review processes. + Familiarity with cleaning verification and validation processes. INDBH We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.