Laboratory Associate II, GMP
Synthego, Redwood City, CA, United States
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.
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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.
#J-18808-Ljbffr