Scientist, Process Development

Leading or being actively involved in process development projects including oligonucleotide synthesis activities, process development, optimization and scale-up. Working closely with process sciences and cross-functional teams within the organization. In-process analytical method development and utilization. Communicate relevant information and results to CMC development department as well as other key stakeholders throughout the organization. Creation, review, and usage of SOPs and batch records employed for the in-house non-GMP oligonucleotide manufacturing. Technical protocols and reports authoring and reviewing. PhD in Organic/Medicinal Chemistry, Chemical Engineering with 1-3 years post degree experience, preferably in an industrial setting. Strong experience and knowledge in oligonucleotide synthesis, purification, and characterization. Hands-on experience in automated solid-phase DNA synthesizer, demonstrated strong operational execution and problem-solving skills. Experience in analytical techniques (pH, HPLC, LC-MS etc.), or related hands-on experience, is preferred. Ability to work within cross-functional teams and work as a team player. Ability to lead projects and demonstrate strong oral & written communication, and presentation skills. Strong experience in record-keeping and excellent laboratory documentation practice are required. Strong commitment to preserving a high laboratory and scientific standard; maintaining a safe, clean, and orderly laboratory work environment.