Synthego is enabling genome engineering at scale with a blend of scientific instrumentation, industrial automation, and data science. Our team of scientists and engineers are putting multidisciplinary fields together to solve problems that no one field can tackle alone.
We are searching for a motivated and enthusiastic individual to join our Chemistry Development team to improve our oligonucleotide manufacturing process and to directly contribute to launching new oligonucleotide products. As a Process Development Engineer at Synthego, you will have direct responsibility for the development of new techniques for synthesis and purification of RNA and DNA from nanomole to millimole scales. Primary goals include scaling manufacturing processes, improving cost and margin, improving quality of oligonucleotide products, and reducing production times. This role will include developing in both a research and clinical environment, as well as transferring technology into the manufacturing lines. With a focus on the successful introduction and adoption of new technologies in operations, this role will collaborate closely with the hardware, software, operations, quality, and product teams.
What You'll Do:
Design, develop, and implement methods to scale oligonucleotide synthesis and purification
Synthesize, purify and analyze oligonucleotides to specifications, using proprietary and commercial instrumentation
Analyze data from assays such as UV, chromatograms and mass spectrometry for optimizing experimental conditions and determining root causes of failures
Work alongside a cross-functional group of Chemists, Engineers, and Scientists to execute developmental processes and collaborate on designed experiments.
Conduct experimentation using automated instrumentation and liquid handling equipment
Write development protocols and reports and regularly present findings to interdepartmental stakeholders
Conduct IQ/OQ/PQ for new instrumentation acquired for development projects
Practice continuous improvement by contributing ideas and suggestions to new and existing processes
Generate and maintain records or documents in a detailed and consistent manner
Assist with Quality data management, including writing new or updating Standard Operating Procedures, Batch Records, and Change Control documents
Work with vendors to acquire reagents, consumables, or instrumentation as needed for development efforts
Train others on new or updated processes and procedures
About You:
BS in Chemistry, Chemical Engineering, Bio-engineering or a similar field
2-5 years of industry experience within a research/manufacturing/production environment, preferably in a small company/start-up setting
Direct experience in the synthesis and analysis of oligonucleotide products
Experience in data analysis with languages such as Python, SQL.
Understanding of aseptic handling techniques, including liquid handling, pipetting, reagent preparation, and consumables.
Experience using larger scale instrumentation such as HPLCs, oligonucleotide or peptide synthesizers, tangential flow filtration, and/or liquid handlers.
Strong desire to work in a fast-paced, collaborative start-up environment
Demonstrates strong interpersonal and communication skills (both written and oral)
Demonstrates ability to work independently and as part of a team to curate and execute development projects.
Nice to Have:
Deep knowledge of oligonucleotide chemistry or reagent manufacturing, specifically using fluorophores, quenchers, or other oligonucleotide modifiers
Familiar with qPCR
Familiar with fluorescence assays and how to create functional tests for newly developed products
Familiar with biotechnical instrumentation in aspects such as coding new methods, data analysis pipeline, servicing, etc
Company Perks & Benefits:
Medical, dental, and vision benefits
401k Program
Catered meals on Tuesday and Thursday
Paid parental leave
Flexible paid time off
Education Reimbursement Program
