Process Engineer II

Insmed Inc. • Bridgewater, NJ • 15h ago

Company Description Insmed is a global biopharmaceutical company on a mission to transform the lives of patients living with serious and rare diseases. Our most valuable resource is our employees, and everything we do is motivated by a patients-first mentality. We are dedicated to growing our team with talented individuals from around the world who are willing to challenge the status quo, solve problems, and work collaboratively with a sense of urgency and compassion. Guided by our core values of collaboration, accountability, passion, respect, and integrity, we aim to foster an inclusive, diverse, and flexible work environment, where our employees are recognized for leaning in and rolling up their sleeves. If you share our vision and want to work with the most dedicated people in the biopharma industry, come to Insmed to accelerate your career. Recognitions Consistently Ranked Science 's Top Employer Insmed is dedicated to creating a collaborative environment where our team can thrive. Every day, our employees turn their passion for science and research into innovative solutions for patients. That's why we've been named the No. 1 company to work for in the biopharma industry in Science 's Top Employers survey for four years in a row.A Certified Great Place to Work We believe our company is truly special, and our employees agree. In July 2025, we became Great Place to Work-certified in the U.S. for the fifth year in a row. We are also honored to have been listed on the Best Workplaces in Biopharma, Best Workplaces in New York, PEOPLE Companies That Care, Best Workplaces for Women, Best Workplaces for Millennials, and Best Medium Workplaces lists. Overview The Process Engineer II will have responsibility for process development, process characterization, scale-up, and technology transfer activities, supporting new and existing pharmaceutical products. Responsibilities Contribute to the design and execution of process development and process engineering experiments for fermentation /chromatography or other project related processes. Key member of a dynamic, scientifically driven team, dedicated to the development and optimization of robust manufacturing processes for drug products. Key contributor to process development strategies to define manufacturing processes for clinical and commercial products. Apply fundamental engineering principles to characterize and solve process challenges across multiple unit operations, using both experimental and process simulation/modeling approaches. Apply appropriate research tools, instrumentation, technologies, and methodologies to support efficient and effective drug product process development. Manage external vendors and contractors as related to drug product manufacturing services and products. Maintain safety, regulatory, and compliance standards as they relate to the development of pharmaceuticals. Prepare technical reports, publications, and oral presentations.Position Requirements: Bachelor's degree with 5+ years of pharmaceutical experience strongly preferred. Strong background in fermentation/chromatography purification of biopharmaceutical proteins both small scale and large scale. Strong background operating fermentation/chromatography equipment in the preparation of proteins at small and large scale. Extensive experience in pharmaceutical development as it relates to process development/optimization. Demonstrated capability in execution of an experimental program to address issues of process robustness, productivity, and cost, integrating efforts with specialists in other technical disciplines. Proven record of implementing novel and creative solutions to overcome process development obstacles. Working knowledge of quality systems, Quality by Design, validation principles for product and manufacturing processes, engineering design, and statistical process control fundamentals. Solid understanding of GLPs and cGMPs during pharmaceutical develop

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