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RxSight

Post-implantation adjustable intraocular lens system

Senior Scientist - Analytical Chemistry

Biomedical Engineering & Medical DevicesConfirmed live in the last 24 hours
Full-timeAliso Viejo, CA, USA$130k - $160k /yrIn-person

About the Job

Requirements

  • Strong foundation in analytical chemistry and method development.
  • Experience developing, validating, troubleshooting, and transferring analytical methods.
  • Hands-on expertise with chromatographic techniques including gas chromatography-mass spectrometry, gas chromatography-flame ionization detector, headspace gas chromatography, high-performance liquid chromatography/ultra-performance liquid chromatography, liquid chromatography-mass spectrometry, and gel permeation chromatography/size-exclusion chromatography.
  • Experience interpreting chromatographic and mass spectrometric data and developing scientifically defensible conclusions.
  • Knowledge of extractables and leachables testing, impurity characterization, degradation-product analysis, and chemical characterization principles.
  • Familiarity with spectroscopic techniques including Fourier-transform infrared spectroscopy, Raman spectroscopy, ultraviolet-visible spectroscopy, nuclear magnetic resonance, and related analytical methods.
  • Hands-on experience with relevant materials-characterization techniques, such as thermogravimetric analysis, differential scanning calorimetry, tensile testing, and nanoindentation, and the ability to integrate these results with chemical characterization data.
  • Working knowledge of polymeric and biomaterial systems sufficient to support analytical investigations involving silicone- and acrylic-based materials and to connect chemical composition, structure, processing, aging, and degradation with observed material and product behavior.
  • Strong statistical analysis, experimental design, and data interpretation skills.
  • Excellent technical writing and documentation abilities.
  • Ability to work independently while collaborating effectively with materials scientists, optical scientists and engineers, mechanical engineers, process engineers, quality professionals, manufacturing personnel, regulatory partners, and external laboratories.
  • Ph.D. in Analytical Chemistry, Chemistry, Polymer Chemistry, Materials Science or a related scientific discipline with substantial analytical training.

Responsibilities

  • Develop, optimize, qualify, validate, and execute analytical methods supporting product development, design verification, manufacturing support, and regulatory submissions.
  • Perform analytical testing and data interpretation using chromatographic, spectroscopic, and related techniques including gas chromatography-mass spectrometry, gas chromatography-flame ionization detector, headspace gas chromatography, high-performance liquid chromatography/ultra-performance liquid chromatography, liquid chromatography-mass spectrometry, gel permeation chromatography/size-exclusion chromatography, Fourier-transform infrared spectroscopy, Raman spectroscopy, ultraviolet-visible spectroscopy, and related methodologies.
  • Serve as the technical lead for chemical characterization of materials and finished devices, including extractables and leachables, hydrolytic stability, photostability, and other studies conducted in accordance with applicable ISO 11979 and ISO 10993 requirements. Own analytical strategy, method selection, study execution, data analysis, scientific interpretation, and reporting.
  • Characterize impurities, residues, additives, degradation products, process residuals, and other chemical species associated with ophthalmic materials and finished devices, and assess their likely source and relevance to product performance or safety.
  • Collaborate with research and development functions, including materials scientists, optical and mechanical engineers, and process engineers, as well as Operations, to investigate product performance, material changes, aging effects, process interactions, and development-related technical issues and to recommend scientifically justified next steps.
  • Train and mentor junior laboratory staff in sample preparation, routine analytical testing, data quality expectations, and safe, compliant laboratory practices.
  • Author analytical protocols, test methods, validation reports, technical reports, summaries, and supporting documentation for regulatory submissions.
  • Analyze and interpret complex datasets and communicate results and recommendations to cross-functional teams.
  • Lead or support root-cause investigations involving materials, finished products, manufacturing processes, analytical methods, and process or material changes. Integrate analytical results with input from materials scientists and engineers to identify likely mechanisms, evaluate competing hypotheses, and recommend corrective or development actions.
  • Collaborate with Analytical Chemistry Quality Control and external laboratories to transfer methods, review data packages, resolve analytical issues, and ensure data integrity.
  • Evaluate and implement new analytical technologies and methodologies to expand laboratory capabilities.
  • Maintain laboratory organization, instrumentation readiness, and compliance with applicable procedures and quality requirements.

Desired Qualifications

  • Working knowledge of Food and Drug Administration-regulated product development and applicable analytical and chemical-characterization expectations under ISO 11979 and ISO 10993 is preferred.
  • Three or more years of relevant industrial analytical chemistry experience in product development, verification, manufacturing support, or troubleshooting in medical devices, pharmaceuticals, biomaterials, or another regulated technical environment is preferred.
  • Demonstrated experience applying analytical methods to polymeric or biomaterial systems, including silicones, acrylics, hydrogels, or related soft materials, is highly desirable.
  • Experience with chemical characterization such as extractables and leachables, hydrolytic and photostability studies, method validation, and regulatory-supporting analytical activities is preferred.
  • Exposure to polymeric or biomaterial systems, including silicones, acrylics, hydrogels, or related materials, is highly desirable.
  • Experience supporting Food and Drug Administration-regulated products or equivalent quality systems is preferred.

About the Company

RxSight

Post-implantation adjustable intraocular lens system

RxSight develops medical devices for vision correction in cataract surgery. Its flagship product is the Light Adjustable Lens (LAL), an intraocular lens that can be adjusted after implantation using a Light Delivery Device (LDD) to achieve the best possible vision. How it works: after the LAL is implanted, doctors use controlled light exposure via the LDD to fine-tune the lens power post-operatively, allowing precise refractive outcomes before finalizing vision. How RxSight differs from competitors: instead of relying on fixed lenses, it offers an adjustable lens system that enables post-operative customization, paired with a dedicated delivery device and support for ophthalmologists and clinics to optimize patient results. Its goal is to improve quality of life for patients with cataracts and corneal astigmatism by delivering superior, individualized visual outcomes and expanding access to precise vision correction in the cataract market.

Company size
201-500
Company stage
IPO
Headquarters
Aliso Viejo, CA
Founded
1997

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