Process Development Chemist II

Must have a minimum of 2 years of practical experience working in an organic or bioprocess laboratory.
Bachelor’s degree in chemistry, Chemical Engineering, or a related field.
Proficiency working with HPLC, UV, and pH equipment.
Proven ability to provide technical support in root cause failure analysis for production and quality incidents.
Outstanding record-keeping of production activities, experimental procedures, and analytical data.
Maintain the chemistry laboratory space in strict compliance with safety regulations.
Ability to provide technical customer support and routine progress updates to clients, in conjunction with the project manager assigned to each specific project.
Self-motivated with the capacity to work independently as well as collaboratively in teams.
Strong professional presence and meticulous attention to detail.
Technical proficiency that ensures effective execution of detailed procedures.
Demonstrated experience with common computer software packages (Windows, MS Office, etc.).
Capable of multitasking in a fast-paced environment.
Excellent communication and problem-solving skills.

No responsibilities provided.

Master’s degree in chemistry, Chemical Engineering, or a related field.
Expertise in optimizing and scaling up/down solid-phase oligonucleotide synthesis, purification, conjugation, and downstream processing methods in preparation for handover to routine manufacturing.
Experience providing technical and early-stage manufacturing support in the development of therapeutic GMP manufacturing processes and capabilities, including drafting manufacturing procedures.
Extensive experience in nucleoside, nucleotide, nucleic acid, or oligonucleotide chemistry.
Proven experience in process development, process transfer, scale-up/down modeling, equipment, and Unicorn software.
Experience in solid-phase oligonucleotide synthesis chemistry, anion-exchange, and/or reverse-phase chromatography.