Principal Engineer

Role: Senior engineering professional responsible for leading complex technical projects within biopharma, applying advanced scientific and engineering knowledge to ensure quality, compliance, and innovation. Responsibilities: design and execute medium- to large-scale projects, conduct risk assessments, manage project controls, and collaborate with cross-functional teams including marketing, manufacturing, and regulatory functions. Focus on optimizing processes and equipment, integrating regulatory and operational considerations, and mentoring team members. Requirements: Bachelor's degree in engineering, science, or related field; 8+ years of significant engineering or operational experience; proven technical contributions and project management skills. Preferred: background in healthcare, medical devices, biologics, or pharmaceuticals; experience with product/process development; familiarity with financial systems. High-Value: emphasis on complex process or product development in biopharma, with a likely focus on biologics or medical devices, supporting regulatory compliance, validation strategies, and cross-functional collaboration. Work setup and travel details are not specified.