Jobs Companies CSBio Microbiology Technician

Sobre esta vaga de Microbiology Technician na CSBio

CSBio · Presencial · Milpitas, California, United States

CSBio is a peptide contract manufacturer founded in 1993, serving research organizations and pharmaceutical companies worldwide with automated synthesizers and high quality cGMP peptides. We operate cGMP peptide production facilities in Menlo Park, CA, and passed an FDA inspection in 2017 that recommended us for commercial drug substance manufacturing. In 2023, we added cGMP clinical production capacity in Milpitas, CA.

Position Summary

CSBio is seeking a detail-driven Microbiology Technician to join our QC Microbiology laboratory at our Milpitas facility. You will primarily perform bacterial endotoxin and bioburden testing on peptide intermediates, APIs, and drug products, with a focus on our GMP programs. This is an ideal role for a recent BS graduate or early-career technician looking to build a career in pharmaceutical QC microbiology; full training will be provided. Fully on-site at our Milpitas facility.

Job Responsibilities

•   Endotoxin testing: Perform LAL-based bacterial endotoxin testing (USP <85>) on in-process samples, APIs, drug products, and water.

•   Bioburden testing: Perform microbial enumeration and tests for specified microorganisms (USP <61> / <62>) on raw materials, intermediates, and finished product.

•   Monitoring support: Assist with environmental monitoring of cleanrooms and water-system monitoring; read, enumerate, and record microbial growth.

•   cGMP documentation: Record raw data and results in worksheets and LIMS per cGMP and ALCOA+ data-integrity practices; support OOS/OOT investigations and deviations.

•   Clinical batch support: Support timely testing and release of API and clinical batch products to production timelines.

•   Lab operations: Prepare and quality-check media and reagents; maintain aseptic technique, equipment, and laboratory supplies; and perform other QC micro duties as assigned.

Why This Role

You will learn compendial endotoxin and bioburden testing end-to-end in an FDA-inspected cGMP environment, working alongside an experienced Microbiology Lead on testing that directly enables clinical and commercial peptide products to reach patients.

Requirements

•   BS degree in Microbiology, Biology, Biochemistry, Biotechnology, or a related life-science discipline. An Associate degree with relevant laboratory experience will be considered.

•   0–2 years of laboratory experience; academic, internship, or co-op laboratory experience qualifies for entry-level candidates.

•   Working knowledge of aseptic technique and basic microbiology laboratory practices.

•   Careful, accurate documentation habits, strong attention to detail, and the ability to follow written procedures precisely.

•   Able to commit to a full-time, fully on-site role at the Milpitas facility, including occasional off-shift or weekend hours to meet clinical batch testing timelines.

•   Ability to wear sterile cleanroom gowning (including face masks, gloves, and safety glasses) for extended periods.

•   Ability to lift up to 25 lbs (e.g., media prep supplies, autoclave loads).

•   Good manual dexterity for precise pipetting and sample handling.

Nice to haves:

◦    Hands-on experience with bacterial endotoxin (LAL) testing and/or bioburden / microbial enumeration methods (USP <85>, <61>, <62>).

◦    Exposure to a cGMP, pharmaceutical, biotech, or other regulated laboratory environment.

◦    Familiarity with environmental monitoring, water-system monitoring, or media preparation.

◦    Experience with LIMS and electronic data-recording systems, and understanding of data integrity (ALCOA+) and good documentation practice (GDP).

Benefits

•   Medical, dental, and vision insurance (Kaiser HMO or BlueShield PPO. Employer pays 90% for Employee and 75% for Employee's family; Dental: Aetna Dental, Delta Dental, Guardian Dental, MetLife Dental. Vision: VSP and Aetna EyeMed)

•   401k 10% 1:1 match

•   PTO policy. 10 days PTO

•   Companywide paid holiday during: Week of July 4, Thanksgiving (2 days), Week of December 25

•   Basic life ($20,000 paid by company) and supplemental life insurance (optional supplemental).

•   Disability insurance 50% standard employer paid.

•   Carpool, clean air vehicle, and cell phone reimbursement

•   Employee rewards and recognition program

•   Company organized social events

•   Quarterly sponsored team building activities

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Sobre a CSBio

CSBio is a leading peptide and peptide synthesizer manufacturing company located on the edge of Silicon Valley in Menlo Park, California. Since 1993, CSBio has been providing high quality custom peptides, cGMP peptides and automated peptide synthesizers to the global biotech community. Our peptide products and peptide synthesis equipment can be found in peptide production laboratories and pharmaceutical companies worldwide.

Our state of the art cGMP manufacturing facility provides cGMP peptides for preclinical and clinical programs and our commercialization and regulatory teams can take you from toxicology studies through market commercialization. CSBio has recently received a Recommendation For Approval from the USFDA following an extensive USFDA PAI audit. Our Quality and Regulatory teams can assist our clients in every step of the clinical study and commercialization processes. We are committed to helping our clients reach the ultimate goal of FDA approval and subsequent commercialization.

CSBio’s product line also includes a complete list of generic peptide APIs including the most widely used peptide APIs in the industry. CSBio now also offers solid phase peptide synthesis resins as well as high quality Fmoc and Boc protected amino acids for use in both R&D and cGMP peptide manufacturing. Whatever your peptide requirements, CSBio can assist you in reaching your ultimate goals by offering high quality products and world class support.

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