Analytical Chemist

Hubot, Inc. is an FDA-registered contract development and manufacturing organization (CDMO) serving global pharmaceutical and personal care brands - including Fortune 500 clients. With 25-30% projected year-over-year growth through 2030, we're building the infrastructure, systems, and team to match world-class ambition.

This position is not eligible for visa sponsorship.

Growth-Stage Opportunity We're forecasting 25-30% year-over-year revenue growth through 2030. This is a rare chance to join a scaling CDMO where your contributions directly shape laboratory capabilities not just maintain them.

Real Client Impact You'll work on products that ship to Fortune 500 pharmaceutical and personal care brands. Your analytical work isn't academic it releases product, supports regulatory submissions, and protects patients and consumers.

Regulated Industry Depth Our laboratory operates under FDA 21 CFR 210/211, ISO 13485, ISO 9001, ISO 14001 and ISO 22716 cGMP standards. You'll sharpen expertise in frameworks that are valued across the global pharmaceutical and personal care supply chain.

Ownership Over Systems, Not Just Instruments You'll hold supervisory sign-off authority in LIMS, author the SOPs your team works from, and drive method development from concept through validation with real technical autonomy.

A Defined Path Forward We promote from within. Strong performers move into Principal Chemist, Method Development Lead, and ultimately Analytical Sciences Manager with mentorship from senior technical leadership and visibility across client programs from day one.

We're hiring a Analytical Chemist to serve as a technical anchor in our method development and analytical sciences function. This is a hands-on, high-ownership role you'll independently develop, validate, and troubleshoot complex analytical methods, mentor junior scientists, and serve as a trusted point of contact for internal teams and external clients alike.

This is not a routine testing position. We're looking for someone who is energized by complex problems, takes pride in airtight documentation, and wants to do meaningful work with real pharmaceutical and consumer products that reach patients and consumers every day.

• Independently develop, evaluate, validate, and verify analytical methods across chromatographic and spectrophotometric platforms HPLC, GC, UV/Vis, FTIR, and titration
• Apply methods to excipients, new chemical entities, drug products, and stability samples
• Support cleaning validation method development and associated sample testing
• Serve as the go-to troubleshooting resource for method performance issues - identify root causes, document critical factors, and resolve problems efficiently and cost-effectively
• Interpret complex data sets, compare results against specifications, and prepare clear, defensible reports
• Trend data to proactively flag concerns and identify process improvement opportunities
• Author SOPs, analytical testing procedures, batch release testing forms, and document templates for team-wide use
• Serve as the site's resident LIMS expert, including supervisory sign-off authority for electronic reports

• Ensure proper use, calibration, and care of reference standards, timers, thermometers, and analytical instrumentation
• Follow all method instructions and internal SOPs to minimize repeat testing, deviations, and investigations
• Review routine laboratory work completed by junior analysts for accuracy and GMP compliance
• Support laboratory management in the preparation and execution of investigations, deviations, and CAPA
• Serve as a technical point of contact for laboratory testing support providing timely, clear updates to supervisors and clients
• Support…