GMP Laboratory Associate II – Oligonucleotide Synthesis

Synthego; Redwood City (CA); On-site; USD 50,000 - 70,000; Full time

Job summary

A biotechnology pioneer in Redwood City is seeking a Laboratory Associate to operate synthesis operations for clinical grade oligonucleotides. The ideal candidate has a Bachelor's degree in chemistry, 1-2 years of experience in a GMP or GLP-regulated environment, and great communication skills. Responsibilities include managing complex lab equipment, ensuring inventory is stocked, and collaborating with cross-functional teams. The company fosters a fast-paced, collaborative startup culture and offers a unique opportunity to contribute to advancing CRISPR technologies.

Qualifications

• 1–2 years of experience in a GMP or GLP-regulated manufacturing environment.
• Must be able to lift/move up to 25 pounds.
• Must be able to sit and/or stand for extended periods up to four hours at a time.

Responsibilities

• Operate and verify synthesis operations for clinical grade oligonucleotides.
• Collaborate with Supply chain, Quality Assurance, and Warehouse teams.
• Troubleshoot routine process and equipment issues under supervision.

Skills

Understanding of quality concepts

Great communication skills

Strong interpersonal skills

Ability to work independently

Education

Bachelor’s degree in chemistry or a related field

Tools

Chromatography systems

Job description

A biotechnology pioneer in Redwood City is seeking a Laboratory Associate to operate synthesis operations for clinical grade oligonucleotides. The ideal candidate has a Bachelor's degree in chemistry, 1-2 years of experience in a GMP or GLP-regulated environment, and great communication skills. Responsibilities include managing complex lab equipment, ensuring inventory is stocked, and collaborating with cross-functional teams. The company fosters a fast-paced, collaborative startup culture and offers a unique opportunity to contribute to advancing CRISPR technologies.