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HomeCompaniesHcfa Fa Us2 Oraclecloud Com CXScientist, Analytical Chemistry

Scientist, Analytical Chemistry

Hcfa Fa Us2 Oraclecloud Com CX · Brookhaven, NY, United States; Brookhaven, Brookhaven, NY, US · On Site · Active · $83,000–$103,000 / year · Oracle Recruiting Cloud / Fusion HCM

Job facts

FieldValue
CompanyHcfa Fa Us2 Oraclecloud Com CX
TitleScientist, Analytical Chemistry
Normalized title-
Department / teamAnalytical Chemistry
LocationBrookhaven, NY, United States
Work modelOn Site
Employment typeFull Time
Salary$83,000–$103,000 / year
Statusactive
ATS providerOracle Recruiting Cloud / Fusion HCM
Posted / first seen2026-06-12 / 2026-06-13
Changed / last seen2026-06-16 / 2026-06-18

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City jobsActive postings in Brookhaven.Open
Department jobsActive postings in Analytical Chemistry.Open
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Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyHcfa Fa Us2 Oraclecloud Com CX
Source883d3ac1-899e-4648-b63e-68f77e57060e
ATS providerOracle Recruiting Cloud / Fusion HCM

Description

Description Description: The Scientist, Analytical Chemistry is a mid-level analytical scientist opportunity supporting the analytical development of pharmaceutical oral dosage form. Fulfills a critical role in supporting the analytical development and validation/verification and method transfer of testing methods for the Quality control laboratory, to characterize drug substance, raw materials, and drug products. The individual is a part of the Quality Control Technical Services (QCTS) team which perform release testing of API, Excipients/raw materials, In-process and Finished products and stability study, cleaning verification samples following written procedures and applicable SOPs, calculate and report results on applicable specification documents. Essential Functions: Perform physical and chemical analysis of raw materials, in-process, and finished pharmaceutical products, including products on stability, according to written methods, material specification, and company policies as identified in standard operating procedures (SOPs). Comply with cGMps, SOPs, and STPs to avoid out-of-specification situation. Assure compliance with state and federal regulations. Use sonic sifter, laser diffraction, Karl Fischer, UV-Vis spectrophotometer, Infra-red spectrophotometer, HPLC with UV detection as well as with conductivity detection, TLC, pH meter, and dissolution. Calibrate HPLC, Dissolution apparatus equipped with auto-sampler and /or in-line UV, pH meters, analytical balances, and Karl-Fischer titrator. Develop and validate analytical methods (mostly LC and GC) for active pharmaceutical ingredients, excipients and dosage forms to be used in the analytical laboratory for routine analysis. Development and optimization of new and existing analytical methods for qualification, release testing of products. Provide training and guidance to laboratory analysts and group members aimed at developing technical capabilities. Expand analytical capabilities of the Analytical Group. Document steps followed during analysis execution, calculate and report results. Actively participate in investigation of laboratory results. Review laboratory analysis data for completeness, specification compliance, and compliance with company’s written policies. Provide timely responses to internal and external inquiries. Evaluate, recommend and implement new analytical technologies and instrumentation for testing Additional Responsibilities: Stays abreast of new developments in analytical technologies. Contributes to improvement in laboratory operations to increase efficiency and GMP compliance. Leads team members on assigned projects, as required. Participates and leads scientific discussions on projects with cross-functional team. Assist the laboratory supervisor with handling non-routine special projects requiring activities such as out-of-specification investigations and out-of-alert limit investigations in the laboratory. Qualifications Education: Bachelors Degree (BA/BS) in chemistry or other relevant pharmaceutical sciences - Required Master Degree (MS/MA) in chemistry or other relevant pharmaceutical sciences - Preferred Experience: 3 years or more in pharmaceutical experience (with Bachelor's Degree) 1 year or more in pharmaceutical experience (with Master's Degree) Specialized Knowledge: Broad knowledge of modern analytical equipment and techniques. Must possess in-depth knowledge of analytical chemistry techniques, such as spectrophotometric, dissolution and drug release, chromatographic techniques and measuring physical parameters (viscosity, particle size or droplet size by laser diffraction, melting point by DSC, water content by TGA, identification by XRPD, and other techniques). Must be able to follow compendial (USP/EP/BP/JP) procedures for analysis. Must understand and apply cGMP requirements applicable to quality control laboratory. Extensive experience in cGMP laboratory testing of pharmaceuticals. Hands-on experience with HPLC, GC, Dissolution Apparatus, UV Spectrophotometer, FTIR, TLC, and MS. Method development and validation experience. Experience writing the standard operating procedures (SOPs) and test methods. Experience with regulatory document compilation. Additional Requirement: This position requires successful completion of an OSHA-compliant Respirator Fit Test. The base salary for this position ranges from $83,000 to $103,000 per year. Amneal ranges reflect the Company’s good faith estimate of base salary that Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, geographic location and other relevant skills. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that helps you enjoy your career alongside life’s many other commitments and opportunities. Company Amneal is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by applicable federal, state, or local laws. If you require a reasonable accommodation to complete the application process or to participate in any part of the hiring process, please contact us at [email protected] . Requests will be handled confidentially and in accordance with applicable laws.

Full job record

Job ID026b1ab7b8f7259754b1d16805335a37e222a6dd
Org ID78a2aa0e-dc9e-4112-a79f-9ca9a23a5ca6
Source ID883d3ac1-899e-4648-b63e-68f77e57060e
Board ID883d3ac1-899e-4648-b63e-68f77e57060e
Provideroracle_hcm
Provider Job Key8172
TitleScientist, Analytical Chemistry
Normalized Title
Statusactive
Activeyes
Location TextBrookhaven, NY, United States; Brookhaven, Brookhaven, NY, US
DepartmentAnalytical Chemistry
Team
Employment Typefull_time
Workplace Typeon_site
Remote Policy
CountryUnited States
RegionNY
CityBrookhaven
Salary RawDescription Description: The Scientist, Analytical Chemistry is a mid-level analytical scientist opportunity supporting the analytical development of pharmaceutical oral dosage form. Fulfills a critical role in supporting the analytical development and validation/verification and method transfer of testing methods for the Quality control laboratory, to characterize drug substance, raw materials, and drug products. The individual is a part of the Quality Control Technical Services (QCTS) team which perform release testing of API, Excipients/raw materials, In-process and Finished products and stability study, cleaning verification samples following written procedures and applicable SOPs, calculate and report results on applicable specification documents. Essential Functions: Perform physical and chemical analysis of raw materials, in-process, and finished pharmaceutical products, including products on stability, according to written methods, material specification, and company policies as identified in standard operating procedures (SOPs). Comply with cGMps, SOPs, and STPs to avoid out-of-specification situation. Assure compliance with state and federal regulations. Use sonic sifter, laser diffraction, Karl Fischer, UV-Vis spectrophotometer, Infra-red spectrophotometer, HPLC with UV detection as well as with conductivity detection, TLC, pH meter, and dissolution. Calibrate HPLC, Dissolution apparatus equipped with auto-sampler and /or in-line UV, pH meters, analytical balances, and Karl-Fischer titrator. Develop and validate analytical methods (mostly LC and GC) for active pharmaceutical ingredients, excipients and dosage forms to be used in the analytical laboratory for routine analysis. Development and optimization of new and existing analytical methods for qualification, release testing of products. Provide training and guidance to laboratory analysts and group members aimed at developing technical capabilities. Expand analytical capabilities of the Analytical Group. Document steps followed during analysis execution, calculate and report results. Actively participate in investigation of laboratory results. Review laboratory analysis data for completeness, specification compliance, and compliance with company’s written policies. Provide timely responses to internal and external inquiries. Evaluate, recommend and implement new analytical technologies and instrumentation for testing Additional Responsibilities: Stays abreast of new developments in analytical technologies. Contributes to improvement in laboratory operations to increase efficiency and GMP compliance. Leads team members on assigned projects, as required. Participates and leads scientific discussions on projects with cross-functional team. Assist the laboratory supervisor with handling non-routine special projects requiring activities such as out-of-specification investigations and out-of-alert limit investigations in the laboratory. Qualifications Education: Bachelors Degree (BA/BS) in chemistry or other relevant pharmaceutical sciences - Required Master Degree (MS/MA) in chemistry or other relevant pharmaceutical sciences - Preferred Experience: 3 years or more in pharmaceutical experience (with Bachelor's Degree) 1 year or more in pharmaceutical experience (with Master's Degree) Specialized Knowledge: Broad knowledge of modern analytical equipment and techniques. Must possess in-depth knowledge of analytical chemistry techniques, such as spectrophotometric, dissolution and drug release, chromatographic techniques and measuring physical parameters (viscosity, particle size or droplet size by laser diffraction, melting point by DSC, water content by TGA, identification by XRPD, and other techniques). Must be able to follow compendial (USP/EP/BP/JP) procedures for analysis. Must understand and apply cGMP requirements applicable to quality control laboratory. Extensive experience in cGMP laboratory testing of pharmaceuticals. Hands-on experience with HPLC, GC, Dissolution Apparatus, UV Spectrophotometer, FTIR, TLC, and MS. Method development and validation experience. Experience writing the standard operating procedures (SOPs) and test methods. Experience with regulatory document compilation. Additional Requirement: This position requires successful completion of an OSHA-compliant Respirator Fit Test. The base salary for this position ranges from $83,000 to $103,000 per year. Amneal ranges reflect the Company’s good faith estimate of base salary that Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, geographic location and other relevant skills. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that helps you enjoy your career alongside life’s many other commitments and opportunities. Company Amneal is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by applicable federal, state, or local laws. If you require a reasonable accommodation to complete the application process or to participate in any part of the hiring process, please contact us at [email protected] . Requests will be handled confidentially and in accordance with applicable laws.
Salary Min83,000
Salary Max103,000
Salary CurrencyUSD
Salary Periodyear
Source URLhttps://hcfa.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/AmnealCareers/job/8172
Apply URLhttps://hcfa.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/AmnealCareers/job/8172
First Seen At2026-06-13 11:49:06Z
Last Seen At2026-06-18 11:19:26Z
Last Checked At2026-06-18 11:19:26Z
Last Changed At2026-06-16 10:55:28Z
Inactive At
Source Posted At2026-06-12 18:22:06Z
Source Updated At
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GET https://api.bluedoor.sh/job-postings/v1/jobs/026b1ab7b8f7259754b1d16805335a37e222a6dd?include=descriptionJSON
GET https://api.bluedoor.sh/job-postings/v1/orgs/78a2aa0e-dc9e-4112-a79f-9ca9a23a5ca6JSON
GET https://api.bluedoor.sh/job-postings/v1/sources/883d3ac1-899e-4648-b63e-68f77e57060eJSON
GET https://api.bluedoor.sh/job-postings/v1/jobs/026b1ab7b8f7259754b1d16805335a37e222a6dd/eventsJSON