Manufacturing Representative - Night Shift

Role: Manufacturing Associate supporting oligonucleotide API production in a GMP-regulated facility. Primary objectives include commissioning, qualification, validation (CQV) of new equipment, and manufacturing at scale. Responsibilities encompass operating and maintaining complex process equipment, assisting with tech transfer and process scale-up, writing SOPs, troubleshooting, and collaborating with engineering, validation, and quality teams to resolve technical issues and support documentation such as CAPAs and deviations. Qualifications: Associate’s or Bachelor’s in a scientific or technical field; 1+ years' GMP manufacturing experience; familiarity with oligonucleotide synthesis, HPLC, lyophilization is advantageous. Skills required include attention to detail, SOP adherence, documentation, troubleshooting, and mechanical aptitude. High-value details: focus on oligonucleotide therapeutics, GMP environment, supporting process validation, equipment calibration, and validation documentation. Work setup: full-time, day shift transitioning to night shift; no travel required.