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Sr. Scientist /Scientist - Pharmaceutical Drug Development

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
TitleSr. Scientist /Scientist - Pharmaceutical Drug Development
Normalized title-
Department / team-
LocationExton, PA, United States
Work model-
Employment typeFull Time
Salary-
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2024-07-30 / 2026-05-31
Changed / last seen2026-06-06 / 2026-06-06

Related slices

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
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
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

Sr. Scientist/Scientist, Pharmaceutical Drug Development Title : Sr. Scientist/Scientist Location: Exton, PA (CMC) Full time 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. Responsibilities: Perform necessary literature and patent search to support studies for development of drug products and generate data/development reports for use by the sponsors as part of their regulatory submissions or patent filings. Plan and perform various stages of product development studies, including pre-formulation, formulation development, process development, optimization, and technology transfer. Incorporate Quality-by-Design tools in drug development. Develop prototype formula and evaluate the predetermined QTPPs and CQAs. Write and review GMP documentation, including manufacturing batch records, and appropriate study protocols, and interface with CTM Manufacturing Team for technology transfer for CTM Batch Manufacturing. Collaborate with team members (Analytical Scientists, Quality Assurance, Material Coordinator, and Manufacturing Technicians) to meet timelines for drug product delivery. Assist department supervisor in collaborating with sponsor(s) to facilitate transfer of knowledge and deliverables of drug product. Follow company policies and conduct work according to appropriate Frontage SOPs and comply with cGMP guidelines. Requirements: PhD in Pharmaceutical Sciences or related fiels with 2-3 years of experience OR MS in Pharmaceutics, Pharmaceutical Science or related field with 7-8 years of experience. In depth knowledge of theory and techniques in drug development and drug delivery. Experience in sterile product development including emulsions, suspensions, and lipid-based delivery systems. cGMP knowledge and hands-on experience in sterile small molecule and Protein/biologics product development is a plus. Strong written, and verbal communication, and presentation skills. Good understanding cGMP, Regulatory Compliance including FDA/EU/ICH guidance with regards to drug development. Salary and Benefit s : 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

Job ID99a253f4bad7fa8be3300cddd5802c05d39a0a5c
Org IDb9d3aab9-695d-4b2b-bd3f-ae58acddd87a
Source ID57b990c1-73e8-474a-b966-75ea19495511
Board ID57b990c1-73e8-474a-b966-75ea19495511
Provideradp_workforcenow
Provider Job Key488256
TitleSr. Scientist /Scientist - Pharmaceutical Drug Development
Normalized Title—
Statusactive
Activeyes
Location TextExton, PA, US, Exton, PA
Department—
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Employment Typefull_time
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CountryUnited States
RegionPA
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 At2024-07-30 14:55:00Z
Source Updated At—
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Develop prototype formula and evaluate the predetermined QTPPs and CQAs.</li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: arial, sans-serif;\">Write and review GMP documentation, including manufacturing batch records, and appropriate study protocols, and interface with CTM Manufacturing Team for technology transfer for CTM Batch Manufacturing.</li><li style=\"margin: 0in; line-height: 115%; font-size: 16px; font-family: arial, sans-serif;\">Collaborate with team members (Analytical Scientists, Quality Assurance, Material Coordinator, and Manufacturing Technicians) to meet timelines for drug product delivery.&nbsp;</li><li style=\"margin: 0in; line-height: 115%; font-size: 16px; font-family: arial, sans-serif;\">Assist department supervisor in collaborating with sponsor(s) to facilitate transfer of knowledge and deliverables of drug product.</li><li style=\"margin: 0in; line-height: 115%; font-size: 16px; font-family: arial, sans-serif;\">Follow company policies and conduct work according to appropriate Frontage SOPs and comply with cGMP guidelines.</li></ul><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:.5in;line-height:115%;font-size:15px;font-family:\"Calibri\",sans-serif;'><span style=\"font-family: arial, sans-serif; font-size: 16px;\">&nbsp;</span></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;line-height:115%;font-size:15px;font-family:\"Calibri\",sans-serif;'><span style=\"font-family: arial, sans-serif; font-size: 16px;\"><strong><span style=\"border: 1pt none windowtext; padding: 0in;\">Requirements:</span></strong>&nbsp;</span></p><ul style=\"list-style-type: disc;\"><li style=\"font-family: arial, sans-serif; font-size: 16px;\">PhD in Pharmaceutical Sciences or related fiels with 2-3 years of experience OR MS in Pharmaceutics, Pharmaceutical Science or related field with 7-8 years of experience.</li><li style=\"font-family: arial, sans-serif; font-size: 16px;\">In depth knowledge of theory and techniques in drug development and drug delivery.</li><li style=\"font-family: arial, sans-serif; font-size: 16px;\">Experience in sterile product development including emulsions, suspensions, and lipid-based delivery systems. cGMP knowledge and hands-on experience in sterile small molecule and Protein/biologics product development is a plus.</li><li style=\"font-family: arial, sans-serif; font-size: 16px;\">Strong written, and verbal communication, and presentation skills.</li><li style=\"font-family: arial, sans-serif; font-size: 16px;\">Good understanding cGMP, Regulatory Compliance including FDA/EU/ICH guidance with regards to drug development.</li></ul><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;line-height:normal;font-size:15px;font-family:\"Calibri\",sans-serif;'><span style=\"font-family: arial, sans-serif; font-size: 16px;\">&nbsp;</span></p><p style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;font-size:11.0pt;font-family:\"Calibri\",sans-serif;line-height:normal;' id=\"isPasted\"><span style=\"font-family: arial, sans-serif; font-size: 16px;\"><strong><span style=\"color: rgb(51, 51, 51);\">Salary and Benefit</span><span style=\"color: rgb(51, 51, 51);\">s</span></strong><strong><span style=\"color: rgb(51, 51, 51);\">:</span></strong></span></p><p style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;font-size:11.0pt;font-family:\"Calibri\",sans-serif;line-height:12.05pt;background:white;'><span style=\"font-size: 16px; font-family: arial, sans-serif; color: rgb(65, 65, 65);\">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-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;font-size:11.0pt;font-family:\"Calibri\",sans-serif;line-height:12.05pt;background:white;'><span style=\"font-size: 16px; font-family: arial, sans-serif; color: rgb(65, 65, 65);\">&nbsp;</span></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:11.0pt;font-family:\"Calibri\",sans-serif;line-height:12.95pt;background:white;'><span style=\"font-family: arial, sans-serif; font-size: 16px;\"><em><span style=\"color: black;\">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></span></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;line-height:normal;font-size:15px;font-family:\"Calibri\",sans-serif;'><br></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;line-height:normal;font-size:15px;font-family:\"Calibri\",sans-serif;'><span style='font-family:\"Times New Roman\",serif;'>&nbsp;</span></p></div></div></div></div>\n",
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