troubleshootinggmpstability testinganalytical chemistrychromatographyspectroscopyanalytical developmentanalytical method development
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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$87к-137к/год
$88к$110кмедиана$120к
По похожим ролям (46) ~ $110к/год
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Текст:
Hirify AI/Оригинал
TL;DR
Scientist, Analytical R&D (2nd Shift) (Analytical Chemistry): Supporting GMP release and stability testing for APIs, pharmaceutical formulations, and manufacturing processes with an accent on analytical method development, laboratory characterization, and statistical data analysis. Focus on validating analytical methods, troubleshooting testing challenges, documenting ALCOA-compliant results, and collaborating with quality, process chemistry, and pharmaceutical operations teams.
Location: Rahway, New Jersey, United States; onsite second-shift role from 3:30 PM to 12:00 AM; US and Puerto Rico residents only
Salary: $87,300–$137,400 annually, plus potential annual bonus and long-term incentive.
Company
hirify.global develops pharmaceutical products and innovative drug delivery technologies and predictive analytical tools to improve human health.
What you will do
Support GMP release and stability testing for active pharmaceutical ingredients, pharmaceutical formulations, and manufacturing processes.
Use traditional and advanced analytical tools to characterize small molecule, peptide, and oligonucleotide development materials.
Validate and implement analytical methods for clinical material testing.
Document experiments, procedures, results, and conclusions according to ALCOA principles; perform data entry and review and author analytical reports.
Troubleshoot GMP testing issues with cross-functional project teams and Quality stakeholders.
Support compliance audits and inspections while collaborating with Analytical R&D, Global Development Quality, Process Chemistry, and Pharmaceutical Operations.
Requirements
Bachelor of Science degree with at least 3 years of relevant industry experience, or a Master of Science degree in Chemistry, Pharmaceutical Sciences, or another Life Science with at least 1 year of relevant industry experience.
Excellent written, oral, and interpersonal communication skills.
Ability to work in a team environment with cross-functional interactions.
Strong analytical chemistry, analytical development, laboratory technique, data entry, data review, stability testing, troubleshooting, and analytical reporting capabilities.
Ability to write standard operating procedures and work with Good Manufacturing Practices.
Ability to work the second shift from 3:30 PM to 12:00 AM.
Must be a resident of the United States or Puerto Rico.
Nice to have
Hands-on experience with GMP operations, advanced chromatographic separation science, spectroscopy analysis, dissolution testing, and other analytical techniques.
Experience with Empower, data science, or LCMS.
Culture & Benefits
Collaborative, cross-functional scientific environment focused on ethics, integrity, inclusion, and improving human health.
Regular employee status with medical, dental, vision, insurance, retirement benefits including 401(k), paid holidays, vacation, compassionate leave, and sick days.
No relocation, travel, or flexible work arrangement; hazardous materials may be involved.
Visa sponsorship is not available.
Hiring process
Applications are accepted through the hirify.global careers site; current employees and contingent workers have separate application routes.
Accommodation support is available during the hiring process upon request.
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