Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
$87к-137к/год
$87к$110кмедиана$120к
По похожим ролям (47) ~ $110к/год
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Роль чётко очерчена и связана с разработкой лекарств и GMP-испытаниями в известной фармацевтической компании; обязательная работа на месте и отсутствие релокации ограничивают доступность.
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Scientist, Analytical Research and Development (GMP/Analytical Chemistry): Supporting laboratory-based analytical characterization and statistical data analysis for small-molecule, peptide, and oligonucleotide drug development with an accent on GMP release and stability testing, analytical method validation, and advanced analytical tools. Focus on troubleshooting cross-functional testing challenges, documenting ALCOA-compliant results, and supporting clinical material testing and compliance inspections.
Location: Onsite in Rahway, New Jersey, United States. The role is for United States, Canada, and Puerto Rico residents; no relocation is offered. Travel requirements: 10%.
Salary: $87,300–$137,400 per year, plus eligibility for an annual bonus and long-term incentive where applicable.
Company
hirify.global develops pharmaceutical products and innovative drug delivery technologies to improve human health.
What you will do
Execute GMP release and stability testing for active pharmaceutical ingredients, pharmaceutical formulations, and manufacturing processes using traditional and advanced analytical tools.
Perform laboratory-based analytical characterization and statistical data analysis for small-molecule, peptide, and oligonucleotide drug development.
Document experimental procedures, results, and conclusions in an organized manner following ALCOA principles.
Troubleshoot GMP testing challenges with cross-functional project teams and Quality stakeholders.
Validate and implement analytical methods for clinical material release and stability testing; perform data entry, data review, and author analytical reports or summaries.
Collaborate with Analytical Research and Development, Global Development Quality, Process Chemistry, and Pharmaceutical Operations, and support compliance audits and inspections.
Requirements
Bachelor of Science with at least 3 years of relevant industry experience, or an MS with some relevant industry experience, in Chemistry, Pharmaceutical Sciences, or another Life Sciences field.
Excellent written, oral, and interpersonal communication skills.
Ability to work in a team environment with cross-functional interactions.
Experience or knowledge in analytical chemistry, analytical development, analytical method development, analytical reports, assays, cell-based assays, chemistry, chromatography, drug formulations, GMP, laboratory information management systems, laboratory techniques, pharmaceutical products, product formulation, and qPCR.
Nice to have
Hands-on experience in GMP operations, advanced chromatographic separation science, dissolution, spectroscopy analysis, and other analytical techniques.
Experience with Empower, data science, and LCMS.
Culture & Benefits
Collaborative cross-functional environment focused on ethics, integrity, scientific innovation, and improving human health.
Medical, dental, vision, and other insurance benefits for employees and families.
Retirement benefits including a 401(k).
Paid holidays, vacation, compassionate leave, and sick days.
Inclusive workplace and equal employment opportunity commitment.
Hiring process
Reasonable accommodations are available during the hiring process upon request.
Employment is subject to United States equal employment opportunity and applicable legal requirements.
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