data sciencetechnical writinggmpchemistrydrug developmentmass spectrometryregulatory submissionsliquid chromatographyanalytical method developmentnuclear magnetic resonance
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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$117к-184к/год
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Текст:
Hirify AI/Оригинал
TL;DR
Senior Scientist, Analytical R&D (Onsite) (Pharmaceutical Analytical Sciences): Developing analytical methodologies for drug substances, dosage forms, combination products, and other modalities with an accent on analytical characterization, imaging tools, data analysis, and GMP testing. Focus on solving analytical development challenges, designing studies for synthetic routes and formulations, supporting regulatory submissions, and leading innovative analytical technology projects.
Location: Onsite in Rahway, New Jersey, United States. Domestic relocation may be available. Travel requirements are listed as 5–10% in the responsibilities section, while the employment details state no travel required.
Base salary: $117,000–$184,200 annually, plus potential annual bonus and long-term incentive.
Company
hirify.global develops pharmaceutical products and innovative drug delivery technologies and predictive analytical tools.
What you will do
Develop analytical methodologies for synthetic small molecules, peptides, oligonucleotides, drug products, combination products, and other modalities.
Implement analytical methods for laboratory development, clinical-supply release, and shelf-life assessment under GMP conditions.
Lead drug-development pipeline projects and innovative technology teams focused on future analytical methods and tools.
Author regulatory submission documents, respond to agency questions, and document work accurately and promptly.
Collaborate with internal and external partners, present results to project teams and cross-functional forums, and participate in scientific organizations, conferences, and publications.
Requirements
PhD in Chemistry, Pharmaceutical Science, or a related discipline; or a master’s degree in these fields plus at least 3 years of pharmaceutical industry experience; or a bachelor’s degree in these fields plus at least 7 years of industry experience.
Proven technical problem-solving and innovative research experience supported by scientific publications.
Excellent written and oral communication skills.
Strong leadership, collaboration, and interpersonal skills.
Experience with analytical method development, assay development, bioanalytical analysis, chemistry, drug development, GMP environments, regulatory submissions, and technical writing.
Experience with liquid chromatography, mass spectrometry, and nuclear magnetic resonance is required in the listed skills.
Nice to have
Large-molecule characterization experience, including oligonucleotides, enzymes, or peptides.
Chromatography method development, analysis, and troubleshooting, including LC or GC.
Advanced analytical techniques such as mass spectrometry or dissolution.
Data science experience.
Culture & Benefits
Collaborative environment focused on ethics, integrity, diverse experiences, scientific excellence, and improving human health.
Regular employment with medical, dental, vision, and other insurance benefits for employees and families.
Retirement benefits including 401(k), paid holidays, vacation, compassionate leave, and sick days.
First-shift daytime schedule; flexible work arrangements are not applicable.
Visa sponsorship is not available.
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