Downstream Process Development, Engineer II

Role: Support downstream biotherapeutics process development as an Engineer II, focusing on purification and recovery experiments. Responsibilities: execute chromatography, ultrafiltration, diafiltration, and viral clearance studies across micro, bench, and pilot scales; maintain lab equipment; document experiments in electronic notebooks; perform data analysis; and contribute to process optimization and continuous improvement. Qualifications: associate degree with 2+ years or bachelor’s in chemical engineering, chemistry, biochemistry, or biotech; experience with bioprocess steps such as chromatography, ultrafiltration, and viral clearance; proficiency in lab data management and basic data analysis; familiarity with process development practices and quality standards. Preferred: experience with digital tools and AI-enabled workflows; knowledge of bioprocess control systems. High-value specifics: biopharma process development, biologics or biosimilars, early- to late-stage development, GxP environment, and working in a regulated lab setting. Collaboration involves working closely with senior process engineers and team members in a controlled environment. Location: Lexington, MA, with potential for shifts and PPE requirements. The role emphasizes adherence to safety and quality protocols specific to biopharma manufacturing.