Laboratory Associate II, GMP

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

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.

What You\'ll Do

• Operate and verify in the synthesis, purification, and fill/finish operations for clinical grade oligonucleotides by following established SOPs
• Operate complex lab equipment systems to manage product formulation through an automated workflow
• Execute batch production records or protocols independently, efficiently, and in compliance with site and quality management system requirements
• Handle chemical solutions
• Ensure laboratory products and supplies are maintained and stocked
• Capture production data in compliance with site and quality management system requirements
• Collaborate with Supply chain, Quality Assurance, Warehouse, and other cross-functional teams to meet deadlines
• Troubleshoot routine process and equipment issues under supervision
• Assist in authoring revisions of SOPs, work instructions, and batch records
• Train other Laboratory Associate team members on manufacturing processes
• Utilize ERP system to submit material requests, track inventory, and support production planning
• Perform batch record review for accuracy, completeness, and compliance prior to submission to Quality

About You

• Bachelor’s degree in chemistry or a related field
• 1–2 years of experience in a GMP or GLP-regulated manufacturing environment
• Understanding of quality concepts and familiarity with Quality Management Systems (QMS)
• Great communication skills and able to work with various personalities
• Strong desire to work in a fast-paced, collaborative startup environment
• Demonstrates strong interpersonal skills, as well as a strong commitment to quality
• Demonstrates ability to work independently and as part of a team
• Must be able to lift/move up to 25 pounds
• Must be able to sit and/or stand for extended periods up to four (4) hours at a time

Nice to Have

• Experience working with oligonucleotides
• Experience working with aseptic fill/finish operations
• Experience working with chromatography systems

Our Mission

Synthego® is a pioneering force in the biotechnology industry, dedicated to advancing the frontiers of CRISPR cell and gene therapies through cutting-edge CRISPR technology and expertise. Our mission is to provide unparalleled access to CRISPR solutions at scale, empowering applications from Discovery to Clinic. Driven by a visionary approach, we strive to accelerate the therapeutic development process with best-in-class CRISPR solutions, simplified licensing & expert guidance, driving the adoption and success of CRISPR-based therapies to benefit all patients.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.