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Scientist

0fad767f F389 40ea B2d1 D8df05098476 19000101 000001 · Exton, PA, US, Exton, PA · Active · ADP Workforce Now Recruiting

Job facts

FieldValue
Company0fad767f F389 40ea B2d1 D8df05098476 19000101 000001
TitleScientist
Normalized title-
Department / team-
LocationExton, PA, United States
Work model-
Employment typeFull Time
Salary-
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2025-05-13 / 2026-05-31
Changed / last seen2026-06-06 / 2026-06-06

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PageWhat it containsOpen
Company jobsActive postings from 0fad767f F389 40ea B2d1 D8df05098476 19000101 000001.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through ADP Workforce Now Recruiting.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Exton.Open
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Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

Company0fad767f F389 40ea B2d1 D8df05098476 19000101 000001
Source57b990c1-73e8-474a-b966-75ea19495511
ATS providerADP Workforce Now Recruiting

Description

Scientist/Sr. Scientist Division/Department: Analytical Services, CMC (Chemistry, Manufacturing, and Controls) Reports to: Manager/Group Leader Full-time Location: Exton, PA Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials. Job Summary The Scientist or Sr. Scientist is responsible for supporting in vitro release Testing /In vivo Release testing on drug products. The scientist’s duties include analytical method development/method validation, protocol/report writing, IVRT/IVPT apparatus maintenance and qualification. Role & responsibilities 1. Hands-on experience in conducting, planning and monitoring In-vitro skin permeation studies and Invitro Release Testing: IVPT/IVRT development, validation, pilot study and pivotal study. 2. Thorough knowledge and complete understanding on FDAs requirement for IVPT studies. 3. Data interpretation and day-to-day troubleshooting related to IVPT studies. 4. Should have experience in review of raw data and protocol/report preparation for development, validation, pilot and pivotal studies. 5. Adhere to compliance and regulatory requirement for in-vitro studies. 6. Implementation and revision of SOP’s related to IVRT and IVPT studies. 7. Good Subject knowledge related to Bio-analytical methods/Bio samples analysis and interpretation of bioanalytical data. 8. To ensure routine calibration and preventive maintenances of IVRT and IVPT lab instruments within timelines. 9. Should have experience in writing justification and design of experiments to address Agency’s deficiencies on IVRT and IVPT. 10. Review and preparation of all study protocols and reports. 11. Interaction with cross functional team and to meet the project timelines. 12. Comfortable handling and/or working with biological tissues such as human skin . 13. Follow company policies and conduct work according to appropriate Frontage SOPs and comply with GLP/cGMP guidelines. Essential Duties & Responsibilities Method development/Validation on IVRT/IVPT testing. Any other drug product testing work. Protocol/Report writing, Data Review. Educational/Training Requirement: bachelor’s degree or above Experience: at least two years of related work experience Knowledge, Skills, and Abilities (KSAs): Clear communication, organization, and teamwork. Travel Requirements: 0% Salary and Benefits : Frontage Laboratories offers a competitive compensation and benefits package including health and dental insurance, a 401(k) plan, disability insurance, and life insurance Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

Full job record

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Source ID57b990c1-73e8-474a-b966-75ea19495511
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Activeyes
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CityExton
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First Seen At2026-05-31 18:30:14Z
Last Seen At2026-06-06 20:27:00Z
Last Checked At2026-06-06 20:27:00Z
Last Changed At2026-06-06 20:27:00Z
Inactive At
Source Posted At2025-05-13 19:04:00Z
Source Updated At
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The scientist&rsquo;s duties include analytical method development/method validation, protocol/report writing, IVRT/IVPT apparatus maintenance and qualification.</span></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><br></p><p style='margin:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:black;'><u>Role &amp; responsibilities</u></span></strong></p><p style='margin:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:black;'>1. Hands-on experience in conducting, planning and monitoring In-vitro skin permeation studies and Invitro Release Testing: IVPT/IVRT development, validation, pilot study and pivotal study.</span></p><p style='margin:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:black;'>2. Thorough knowledge and complete understanding on FDAs requirement for IVPT studies.</span></p><p style='margin:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:black;'>3. Data interpretation and day-to-day troubleshooting related to IVPT studies.</span></p><p style='margin:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:black;'>4. Should have experience in review of raw data and protocol/report preparation for development, validation, pilot and pivotal studies.</span></p><p style='margin:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:black;'>5. Adhere to compliance and regulatory requirement for in-vitro studies.</span></p><p style='margin:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:black;'>6. Implementation and revision of SOP&rsquo;s related to IVRT and IVPT studies.</span></p><p style='margin:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:black;'>7. Good Subject knowledge related to Bio-analytical methods/Bio samples analysis and interpretation of bioanalytical data.</span></p><p style='margin:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:black;'>8. To ensure routine calibration and preventive maintenances of IVRT and IVPT lab instruments within timelines.</span></p><p style='margin:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:black;'>9. Should have experience in writing justification and design of experiments to address Agency&rsquo;s deficiencies on IVRT and IVPT.</span></p><p style='margin:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:black;'>10. Review and preparation of all study protocols and reports.</span></p><p style='margin:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:black;'>11. Interaction with cross functional team and to meet the project timelines.</span></p><p style='margin:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:black;'>12. Comfortable handling and/or working with biological tissues such as human skin .&nbsp;</span></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:black;'>13. Follow company policies and conduct work according to appropriate Frontage SOPs and comply with GLP/cGMP guidelines.</span></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:black;'>&nbsp;</span></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;line-height:12.0pt;'><strong><u><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Essential Duties &amp; Responsibilities&nbsp;</span></u></strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;line-height:12.0pt;'><br></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;line-height:12.0pt;'><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:black;'>Method development/Validation on IVRT/IVPT testing.</span></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;line-height:12.0pt;'><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:black;'>Any other drug product testing work.</span></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;line-height:12.0pt;'><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:black;'>Protocol/Report writing, Data Review.</span></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>&nbsp;</span></strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Educational/Training Requirement:</span></strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>&nbsp;bachelor&rsquo;s degree or above</span></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Experience: </span></strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>at least two years of related work experience</span></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Knowledge, Skills, and Abilities (KSAs):</span></strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>&nbsp;Clear communication, organization, and teamwork.</span></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;line-height:12.0pt;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Travel Requirements: </span></strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>0%</span></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;line-height:12.0pt;'><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>&nbsp;</span></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><u><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:#333333;'>Salary and Benefits</span></u></strong><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:#333333;'>:</span></strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;margin-bottom:7.5pt;background:white;'><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:#414141;'>Frontage Laboratories offers a competitive compensation and benefits package including health and dental insurance, a 401(k) plan, disability insurance, and life insurance</span></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;margin-bottom:7.5pt;background:white;'><em><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:#414141;'>Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.</span></em></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'>&nbsp;</p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;' id=\"isPasted\"><span style='font-size:19px;line-height:107%;font-family:\"Times New Roman\",serif;'><strong>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;&nbsp;</strong></span></p><div><div class=\"fr-view\"><br></div></div></div></div></div></div>\n",
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    "requisitionTitle": "Scientist",
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    "postingInstructions": [],
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    "requisitionLocations": [
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}
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