GMP Chemistry Manufacturing Associate

Singular Genomics; San Diego (CA); On-site; USD 69,000 - 86,000; Full time

Benefits offered by this job

Equity compensation

Job summary

Singular Genomics is seeking a Manufacturing Associate 2 on the chemistry team to produce dye labeled NTPs and other organic compounds used in NGS and Spatial technologies. You will join a fast-paced environment and contribute to both routine production and the development of new manufacturing processes.

The role requires a BS in a scientific field and 3–5 years of GMP experience, experience with chromatography, and maintaining strict cGMP/cGDP production standards.

Qualifications

• Bachelor degree in a scientific field preferred.
• 3–5 years manufacturing organic compounds in a GMP environment.
• Experience with reverse phase, normal phase, and anion exchange chromatography.
• GDP, GLP, GMP experience.
• Familiar with 5S and lean six sigma principles.

Responsibilities

• Manufacture chemical compounds (nucleotides, linkers, triphosphates) using established synthesis schemes.
• Document manufacturing processes on batch records per good documentation practices.
• Submit samples to QC departments and maintain lab inventory.
• Maintain laboratory instrumentation and ensure safe conditions per cGMP/cGDP.
• Operate in a fast-paced environment with shifting priorities.
• Wear full PPE and follow EH&S programs throughout the shift.

Skills

GMP manufacturing experience

Laboratory techniques

Chromatography knowledge

Documentation practices

PPE proficiency

Education

Bachelor of Science in a scientific field

Tools

LC-MS

HPLC

Rotary evaporators

UV-Vis Spectrophotometers

Job description

Singular Genomics is seeking a Manufacturing Associate 2 on the chemistry team to produce dye labeled NTPs and other organic compounds used in NGS and Spatial technologies. You will join a fast-paced environment and contribute to both routine production and the development of new manufacturing processes.

The role requires a BS in a scientific field and 3–5 years of GMP experience, experience with chromatography, and maintaining strict cGMP/cGDP production standards.