Process Engineer - Advanced

Role: Senior Process Engineer leading complex manufacturing process design, optimization, and project management within a GMP biopharma API facility focused on oligonucleotide therapeutics. Responsibilities include troubleshooting, SOP/MBR review, managing capital projects from design through qualification, supporting process transfer and scale-up, and ensuring EHS, validation, and quality compliance. Qualifications: Bachelor's/Master's in Chemical Engineering or equivalent, with 4+ years in pharma/biopharma and fine chemicals; 3+ years managing projects across all phases. Preferred skills include familiarity with ASME BPE standards, control system design (SCADA, PLC), validation protocols, AutoCAD/Visio, and experience with facility layouts, P&IDs, and process troubleshooting. High-value specifics: GMP manufacturing, oligonucleotides, process validation, cross-disciplinary coordination, occasional travel, day shift, located in Frederick, Colorado.