AR&D Scientist

Kelly; Summit (NJ); On-site; USD 55,000 - 69,000; Full time

Benefits offered by this job

Medical benefits

Paid time off

Holidays

401K

Job summary

Kelly Science and Clinical is seeking an Analytical R&D Scientist for an engagement with a global consumer product and pharmaceutical client in Summit, NJ. The role focuses on developing analytical and bioanalytical methods for skin health compounds, performing IVPT analyses, and reporting results using HPLC-MS, HPLC-UV, and HPLC-CAD.

Responsibilities include method development/validation, data documentation, strict SOP and EHS compliance, and collaboration with R&D teams to meet project

Qualifications

• Develop and validate HPLC-MS methods for qualitative and quantitative analysis.
• Perform IVPT sample analyses for formulation screening.
• Document results and write technical reports.
• Ensure EHS compliance and maintain SOPs.
• Independent work and meeting deadlines.

Responsibilities

• Perform analytical testing including sample preparation and method development/validation.
• Develop analytical methods for material characterization and identification.
• Maintain compliance with EHS and SOPs.
• Document data accurately and maintain laboratory notebooks.
• Communicate results with R&D teams and meet project deadlines.

Skills

Analytical testing

Data documentation

Independent work

Team communication

Education

Bachelore2s or Mastere2s degree in Chemistry/Analytical Chemistry/Pharmaceutical Sciences

Tools

HPLC-MS

HPLC-UV

HPLC-CAD

GC-MS

SEM-EDS

TGA/DSC

Job description

Analytical R&D Scientist

Kelly Science and Clinical has an opening for an AR&D Scientist for an engagement at one of our Global consumer product & pharmaceutical clients in Summit, NJ. The role is eligible for medical benefits, paid time off including vacation (PTO), and holidays, and 401K. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.

Schedule

Mon-Fri, 8AM-5PM

Duration: 12mo, can extend

Compensation: $40-$50/hr

Summary

This role is responsible for the development of analytical and bioanalytical methodologies for new compounds in Skin Health and associated molecules to support In Vitro Permeation Test (IVPT) or other associated activities using HPLC-MS, HPLC-UV, or HPLC-CAD as needed. Perform IVPT sample analyses for formulation screening projects. Record experimental data and write analytical reports.

Responsibilities

• Perform analytical testing of samples including but not limited to: Sample preparation and HPLC-MS method development/validation for qualitative and quantitative analysis; Sample analysis of APIs in biological matrices using HPLC-MS.


• Develop analytical methodologies for material characterization and structural identification using various technologies including HPLC-UV, HPLC-CAD, HPLC-MS, and GC-MS, etc.


• Maintain Compliance with EHS requirements;


• Participate in job-related projects, technical and compliance meetings as needed.


• Understand the operation of all applicable lab equipment


• Ability to understand and apply SOPs for documenting and maintaining an accurate laboratory notebook, including sample data for all tests performed


• Proper and timely documentation in instrument logbooks in accordance with current SOPs utilizing the following programs: EMPOWER3, and Microsoft Office Suite


• Understand and follow safety procedures


• Learn additional techniques as needed


• Meet established deadlines for all sample testing


• Daily communication with internal members concerning testing, results, and project plans

Qualifications

• Bachelor’s or Master’s degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related field, with intermediate-level GxP laboratory experience.


• Hands-on experience developing and validating HPLC-MS methods for qualitative and quantitative analysis, including biological matrices.


• Proficiency with HPLC-UV, HPLC-CAD, GC-MS, and related analytical instrumentation; experience with SEM-EDS and TGA/DSC.


• Experience with IVPT, formulation screening, sample preparation, laboratory SOPs, EHS compliance, and accurate data documentation.


• Ability to work independently, meet deadlines, interpret results, prepare technical reports, and communicate effectively with R&D teams


• BSL-2 experience preferred.

What happens next

Once you apply, you’ll proceed to the next steps if your skills and experience look like a good fit. But don’t worry—even if this position doesn’t work out, you’re still in our network. That means all of our recruiters will have access to your profile, expanding your opportunities even more. Helping you discover what’s next in your career is what we’re all about.