Gator Bio is a growing biotech company located in Palo Alto, CA. We develop, manufacture and market instruments, biosensors, reagents, and consumables used by life science research for biotherapeutic characterization, drug discovery, pharmaceutical and vaccine development. Our mission is to simplify and accelerate biological analysis for biotherapeutic research and development.
Gator Bio is looking for an entry level temporary to permanent Quality Control (QC) biochemist who will perform QC tasks, assay development, reagents validation, troubleshooting and documentation based on methodologies and approaches according to strict SOP.
ESSENTIAL DUTIES AND RESPONSIBILITIES
Performing QC testing and validation following written procedures using GMP compliance.
Performing material incoming QC, in-process testing, and final product release.
Preparing reagents, buffers, standards, samples, and controls according to approved procedures.
Multitasking effectively and efficiently to ensure maximum and high-quality output.
Maintaining cleanliness and orderliness of work area .
Performing assay development task based on the project.
Using good documentation practices (GDP) to record original data.
Compliance with all on-going training requirements.
Independently drafting QC protocols or SOP.
Participating in the direction of QC analytical method troubleshooting and in investigations of OOS results.
Coordinating laboratory maintenance activities, including the monitoring of supply inventories, logbooks, and equipment calibration status.
Must be a team player with good communication skills and detail oriented.
Other duties as assigned.
QUALIFICATIONS
BS in biology, chemistry, biochemistry, or other related science.
0 - 2 years’ experience in the related IVD or biotech field.
High level of integrity, flexible, action oriented.
High attention to detail, excellent organizational skills, and ability to work on multiple projects.
Ability for problem-solving and decision-making.
Excellent interpersonal and verbal communications skills.
Proficient in Microsoft Office Suite - Word, Excel, PowerPoint, etc.
POSITION REQUIREMENTS
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 up to 20 lbs.
The ability to lift 30 lbs. chest high will be required.
The role will require long periods of standing and sitting.
The employee will be required to use hands for computer work and pipetting.
Must pass a health screening.
Required biosafety training upon hiring.
Numbers & Facts
Location
Palo Alto, CA
Job Type
Full-time
Skills
Analysis Skillsunmatched
Assay Developmentunmatched
Biochemistryunmatched
Biologyunmatched
Biotech and Pharmaceuticalunmatched
Calibrationunmatched
Chemistryunmatched
Communication Skillsunmatched
Detail Orientedunmatched
Documentationunmatched
Drug Developmentunmatched
Drug Discoveryunmatched
GMP (Good Manufacturing Practices)unmatched
Interpersonal Skillsunmatched
Lift/Move 20 Poundsunmatched
Lift/Move 30 Poundsunmatched
Microsoft Excelunmatched
Microsoft Officeunmatched
Microsoft PowerPointunmatched
Microsoft Wordunmatched
Multitaskingunmatched
Organizational Skillsunmatched
Presentation/Verbal Skillsunmatched
Problem Solving Skillsunmatched
Product Testingunmatched
Quality Controlunmatched
Research & Development (R&D)unmatched
Scientific Researchunmatched
Standard Operating Procedures (SOP)unmatched
Team Playerunmatched
Testingunmatched
Validation Testingunmatched
🎯
Be found by employers
5,500+ employers search our resume database daily. Add yours to get found by recruiters looking for candidates like you.
Level up your application
Professional resume templates
Browse dozens of recruiter approved resume templates, layouts and formats. Choose your favorite and make it your own in minutes.