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2 дня назад

Scientist, Analytical Research and Development

87 300 - 137 400$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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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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