Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
$142к-224к/год
$140к$170кмедиана$190к
По похожим ролям (48) ~ $170к/год
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Хорошая вакансия
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Чётко определённая руководящая научная роль в крупной фармкомпании даёт серьёзную ответственность за GMP-процессы, но постоянная вечерняя смена и работа на месте заметно влияют на образ жизни.
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Вечерняя сменаПонятная зона ответственностиКрупная фармкомпанияПоддержка переезда
Оценка от Hirify AI
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Associate Principal Scientist, Analytical R&D (GxP Supervisor 2nd Shift) (GMP analytical development): Supervising scientists and specialists performing GMP analytical activities for drug substance and drug product during second-shift operations, with an accent on cleaning verification, method validation, solvent release, and in-process testing. Focus on reviewing analytical data, leading investigations and deviations, troubleshooting laboratory work, and ensuring compliant, right-first-time testing for clinical manufacturing.
Location: Rahway, New Jersey, United States; onsite, second-shift evening operations.
Salary: $142,400–$224,100 per year, plus potential annual bonus and long-term incentive.
Company
hirify.global develops pharmaceutical products and drug delivery technologies supported by predictive analytical tools.
What you will do
Supervise specialists and scientists supporting GMP analytical activities for drug substance and drug product.
Lead cleaning verification, method validation, solvent release, and in-process testing during second-shift operations.
Provide hands-on analytical laboratory support for the clinical pipeline.
Document experiments, procedures, results, and conclusions according to ALCOA+ principles.
Review and approve GMP data, analytical reports, and SOPs while overseeing investigations, deviations, and laboratory troubleshooting.
Drive operational excellence, process improvements, cross-functional collaboration, and internal and external compliance audit support.
Requirements
BS or MS in chemistry or a related science with at least 7 years of industry experience in pharmaceutical drug substance and/or drug product development, or a Ph.D. with at least 3 years of such experience.
Excellent scientific communication, creativity, interpersonal, and collaborative skills.
Ability to lead teams to deliver high-quality results against firm deadlines.
Ability to partner with cross-functional teams to drive results.
Experience with analytical method development, analytical testing, assay development, biological assays, cell-based assays, chromatographic techniques, cleaning validations, drug development, HRMS, LC-MS, pharmaceutical process development, PAT, protein analysis, and regulatory compliance audits.
Nice to have
Experience managing a GMP analytical laboratory supporting cleaning verification, IPC, and solvent release.
Experience with laboratory investigations, deviations, and compliance audits.
Culture & Benefits
Regular employee status with medical, dental, vision, insurance, retirement, and 401(k) benefits.
Paid holidays, vacation, compassionate leave, and sick days.
Domestic relocation is listed as available.
Visa sponsorship is available.
Travel requirements are 10%; no valid driving license is required.
Hiring process
Applications are limited to residents of the United States, Canada, and Puerto Rico through the designated application process.
The posting is effective until the day before the listed end date of November 20, 2026.
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