R&D Chemist II

{
  "content_hash": "64f3dad445d369b838b215ee00c5b7ac2b4bfe7e1b326d7a9d4a69feff5899d7",
  "source_hash": "0b2834789526bd015cd1a0aca25abf2b6ecba2aef42a640fce862508ff9cc0c1",
  "last_changed_at": "2026-06-19T13:58:59.576Z",
  "active_status": "active"
}

{
  "dedupe": null,
  "language": "en",
  "location": {
    "raw": "Nephron SC, LLC",
    "city": "West Columbia",
    "region": "SC",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.8
  },
  "salary_max": null,
  "salary_min": null,
  "inferred_at": "2026-06-21T14:28:03.248Z",
  "launch_scope": {
    "reason": "paylocity_production_catalog",
    "included": true,
    "location": {
      "raw": "Nephron SC, LLC",
      "city": "West Columbia",
      "region": "SC",
      "country": "United States",
      "is_remote": false,
      "confidence": 0.8
    },
    "countries": [
      "United States"
    ]
  },
  "remote_policy": null,
  "salary_period": null,
  "workplace_type": null,
  "salary_currency": null
}

{}

{
  "detail": {
    "url": "https://recruiting.paylocity.com/recruiting/jobs/Details/4267055/Nephron-Pharmaceuticals/R-and-D-Chemist-II",
    "job_type": null,
    "pageData": {
      "jobTitle": "R&D Chemist II",
      "moduleName": "Nephron Pharmaceuticals",
      "showSocialWidget": true
    },
    "apply_path": "/Recruiting/jobs/Apply/4267055",
    "html_title": "Nephron Pharmaceuticals - R&D Chemist II",
    "description_html": "<p>&nbsp;&nbsp;</p><p>• Perform research and development projects for established products and new products including but not limited to analytical test method validation/transfer/verification, deformulation, procedures, investigations, and other non-specified projects or initiatives.&nbsp;</p><p>• Plans, organizes, and manages resources on projects to assure technical quality and schedule adherence&nbsp;</p><p>Performs other duties as assigned or apparent</p><p>&nbsp;&nbsp;</p><p><strong>Essential Duties and Responsibilities:</strong></p><p>• Capable of working in a GMP environment and responsible for generating GMP data.&nbsp;</p><p>• Capable of working with different analytical techniques including but not limited to HPLC, UPLC,&nbsp;</p><p>GC, Automatic Titrator, IR, DSC, ICP, and Mass Spectrometry.&nbsp;</p><p>4500 12th Street Extension, West Columbia, SC 29172 • Phone: 800.443.4313 • Fax: 803.926.9853 • nephronpharm.com&nbsp;</p><p>• Responsible for performing different analytical tests for R&amp;D and QC as needed.&nbsp;</p><p>• Responsible for executing research and development projects for established products and new product development with respect to formulation, laboratory investigations, and early process development.&nbsp;</p><p>• Responsible for evaluating new raw materials and components for quality and safety prior to implementation into exhibit batches and GMP production.&nbsp;</p><p>• Responsible for conducting the development and validation of analytical methods for pharmaceutical ingredients and dosage forms, including establishment of specifications.&nbsp;</p><p>• Assist in drafting R&amp;D and QC protocols and report.&nbsp;</p><p>• Performs research and development stability testing as necessary.&nbsp;</p><p>• Participates in the development and implementation of associated programs (e.g. cleaning validation, process validation, GMP compliance, equipment validation, maintenance and use, etc.)&nbsp;</p><p>• Oversee and ensure reports, submission documentation, and development summaries documenting the product development process are available for clients, partners, and health authorities (i.e. FDA)&nbsp;</p><p><strong>Supplemental Functions:&nbsp;</strong></p><ul><li>Performs job duties with minimal supervision.</li></ul><p><strong>Knowledge &amp; Skills:&nbsp;</strong></p><p>• Highly skilled in conducting analysis by LCMS, HPLC, UPLC, GC, FT-IR, UV/Vis spectroscopy as well as wet chemistry techniques, needing little or no guidance.&nbsp;</p><p>• Strong interpersonal, verbal, and written communication skills. Effective organization, multitasking, and problem-solving skills&nbsp;</p><p>• Computer experience (Microsoft Word, Excel, Power Point, Project)&nbsp;</p><p>• Specific expertise, skills and knowledge within research, product development, analytical method development, and troubleshooting gained through education and/or experience&nbsp;</p><p>• The ability and willingness to change direction and focus to meet shifting organizational and business demands&nbsp;</p><p>• The ability to effectively manage one self, demonstrates integrity, be productive under pressure, and achieve development goals&nbsp;</p><p>• Possesses the initiative and follow through to implement, track and achieve on-time completion of projects, as assigned by management.&nbsp;</p><p>• Must strive for continuous improvement in all work activities.&nbsp;</p><p>• The ability to take strategic objectives and accept accountability, motivate and influence others thinks globally and leverages diversity&nbsp;</p>",
    "jsonld_jobposting": {
      "@type": "JobPosting",
      "title": "R&D Chemist II",
      "@context": "https://schema.org",
      "datePosted": "2026-06-18T20:31:32-05:00",
      "description": "<p>Description</p><p>  </p><p>• Perform research and development projects for established products and new products including but not limited to analytical test method validation/transfer/verification, deformulation, procedures, investigations, and other non-specified projects or initiatives. </p><p>• Plans, organizes, and manages resources on projects to assure technical quality and schedule adherence </p><p>Performs other duties as assigned or apparent</p><p>  </p><p><strong>Essential Duties and Responsibilities:</strong></p><p>• Capable of working in a GMP environment and responsible for generating GMP data. </p><p>• Capable of working with different analytical techniques including but not limited to HPLC, UPLC, </p><p>GC, Automatic Titrator, IR, DSC, ICP, and Mass Spectrometry. </p><p>4500 12th Street Extension, West Columbia, SC 29172 • Phone: 800.443.4313 • Fax: 803.926.9853 • nephronpharm.com </p><p>• Responsible for performing different analytical tests for R&D and QC as needed. </p><p>• Responsible for executing research and development projects for established products and new product development with respect to formulation, laboratory investigations, and early process development. </p><p>• Responsible for evaluating new raw materials and components for quality and safety prior to implementation into exhibit batches and GMP production. </p><p>• Responsible for conducting the development and validation of analytical methods for pharmaceutical ingredients and dosage forms, including establishment of specifications. </p><p>• Assist in drafting R&D and QC protocols and report. </p><p>• Performs research and development stability testing as necessary. </p><p>• Participates in the development and implementation of associated programs (e.g. cleaning validation, process validation, GMP compliance, equipment validation, maintenance and use, etc.) </p><p>• Oversee and ensure reports, submission documentation, and development summaries documenting the product development process are available for clients, partners, and health authorities (i.e. FDA) </p><p><strong>Supplemental Functions: </strong></p><ul><li>Performs job duties with minimal supervision.</li></ul><p><strong>Knowledge & Skills: </strong></p><p>• Highly skilled in conducting analysis by LCMS, HPLC, UPLC, GC, FT-IR, UV/Vis spectroscopy as well as wet chemistry techniques, needing little or no guidance. </p><p>• Strong interpersonal, verbal, and written communication skills. Effective organization, multitasking, and problem-solving skills </p><p>• Computer experience (Microsoft Word, Excel, Power Point, Project) </p><p>• Specific expertise, skills and knowledge within research, product development, analytical method development, and troubleshooting gained through education and/or experience </p><p>• The ability and willingness to change direction and focus to meet shifting organizational and business demands </p><p>• The ability to effectively manage one self, demonstrates integrity, be productive under pressure, and achieve development goals </p><p>• Possesses the initiative and follow through to implement, track and achieve on-time completion of projects, as assigned by management. </p><p>• Must strive for continuous improvement in all work activities. </p><p>• The ability to take strategic objectives and accept accountability, motivate and influence others thinks globally and leverages diversity </p><p>Requirements</p><p>  </p><p><strong>Education/Experience: </strong></p><p>• Regionally accredited Master’s Degree in Chemistry and/or a minimum of 8 - 10 years of previous experience in cGMP related environment </p><p><br/></p><p><strong>Working Conditions / Physical Requirements:</strong></p><p>• Position requires typing, climbing, lifting (up to 15lbs), reaching, vision (20/20), standing (10%), sitting (90%), walking, and hearing </p><p>• Additional Requirements: As needed </p>",
      "jobLocation": {
        "@type": "Place",
        "address": {
          "@type": "PostalAddress",
          "postalCode": "29172",
          "addressRegion": "SC",
          "streetAddress": "4500 12th Street Extension",
          "addressCountry": "US",
          "addressLocality": "West Columbia"
        }
      },
      "hiringOrganization": {
        "logo": "https://recruiting.paylocity.com/recruiting/jobs/GetLogoFile?moduleId=9003",
        "name": "NEPHRON SC, LLC",
        "@type": "Organization"
      }
    },
    "requirements_html": "<p>&nbsp;&nbsp;</p><p><strong>Education/Experience:&nbsp;</strong></p><p>• Regionally accredited Master’s Degree in Chemistry and/or a minimum of 8 - 10 years of previous experience in cGMP related environment&nbsp;</p><p><br></p><p><strong>Working Conditions / Physical Requirements:</strong></p><p>• Position requires typing, climbing, lifting (up to 15lbs), reaching, vision (20/20), standing (10%), sitting (90%), walking, and hearing&nbsp;</p><p>• Additional Requirements: As needed&nbsp;</p>",
    "requirements_text": "Education/Experience:\n • Regionally accredited Master’s Degree in Chemistry and/or a minimum of 8 - 10 years of previous experience in cGMP related environment\n Working Conditions / Physical Requirements:\n • Position requires typing, climbing, lifting (up to 15lbs), reaching, vision (20/20), standing (10%), sitting (90%), walking, and hearing\n • Additional Requirements: As needed"
  },
  "list_job": {
    "JobId": 4267055,
    "IsRemote": false,
    "JobTitle": "R&D Chemist II",
    "IsInternal": false,
    "Description": "",
    "JobLocation": {
      "Zip": "29172",
      "City": "West Columbia",
      "Name": "Nephron SC, LLC",
      "Metro": null,
      "State": "SC",
      "County": null,
      "Address": "4500 12th Street Extension",
      "Country": "USA",
      "Address2": null,
      "ModuleId": 9003,
      "LocationId": 4192215,
      "SmartyAddressId": "b754a282-c9bc-4e13-ace0-8de1e1f05f3d"
    },
    "LocationName": "Nephron SC, LLC",
    "PublishedDate": "2026-06-18T15:31:28-05:00",
    "HiringDepartment": null,
    "IndeedRemoteType": 2,
    "ShouldDisplayLocation": true
  },
  "detail_errors": []
}