Senior Research Associate

Gator Bio is a pioneering biotech company dedicated to transforming healthcare through innovative solutions. Located in Palo Alto, California, we develop and deliver cutting-edge bioanalytical tools that empower life science researchers across a wide range of fields. Our mission is to accelerate biological analysis, enabling groundbreaking discoveries in life sciences, drug discovery, and pharmaceutical development. 

We are seeking a highly motivated and experienced Senior Research Associate to play a pivotal role in the development and continuous improvement of our biosensor product. The Sr. RA will assist scientist _ MSAT in process improvement and execute Manufacturing Science & Technology (MSAT) projects. The successful candidate will be responsible for ensuring that our products consistently meet and exceed the highest quality standards, delivering exceptional value to our customers. This role requires strong technical expertise, problem-solving skills, and the ability to work collaboratively within the team and across function groups. 

• Independently design and execute complex laboratory research for Gator label-free detection assay development. 
• Support the Scientist _ MSAT in driving continuous improvement initiatives through proactive monitoring of product quality performance and collaborative identification and implementation of solutions for enhanced quality, efficiency, and cost-effectiveness. 
• Accomplish tasks from the Quality Management System (QMS) related to the investigation of customer complaints and non-conforming reports (NCRs) for Gator consumables.  
• Work closely with the Scientist in MSAT to conduct product transfer activities, which will involve significant interaction and coordination with our international manufacturing team. This includes actively participating in establishing clear communication channels, sharing technical expertise and documentation as directed, and contributing to the collaborative resolution for the successful transition of manufacturing processes across sites. 
• Maintain meticulous documentation in laboratory notebooks, ensuring data integrity, and facilitating knowledge transfer. This also involves diligent creation, maintenance, and adherence to Quality Management System (QMS) documents, including batch records, work instructions, and QC methods. 
• Proactively communicate experimental results, critical analyses, and strategic conclusions to project teams and stakeholders, contributing directly to key decision-making processes in a fast-paced environment 

• Bachelor’s degree in biochemistry, molecular biology, chemical engineering, bioengineering, or other relevant scientific discipline. 
• Minimum of 3-5 years of hands-on experience in a biotech/pharmaceutical laboratory setting, with direct exposure to manufacturing support, process development, or quality control activities. Demonstrated ability to work independently and manage projects with minimal supervision. 
• Prior experience with analytical instrumentation and familiarity with ISO 9001, GMP/GLP regulations is a plus. 
• Working knowledge of bioanalytical assays (e.g., ELISA, or other immunoassays),antibody drug discovery, protein characterization techniques, and experience with Surface Plasmon Resonance (SPR) or BioLayer Interferometry (BLI) in a manufacturing or development context is highly desirable. 
• Strong written and verbal communication skills, including experience in generating technical reports, protocols, and presenting data to cross-functional teams. Familiarity with statistical data analysis and process monitoring is beneficial. 

• To perform this job successfully, an individual must be able to perform each essential duty and responsibility satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. 
• Ability to lift, push, pull, carry, and/or move 20 lbs. 
• This role will require long periods of standing and sitting. 
• The employee will be required to use hands for computer work and pipetting. 
• Required biosafety training upon hiring. 
• Must pass a health screening.