data analysistechnical writingmsassay developmentsample preparationmethod developmentlchplcbiopharmaceuticals
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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$107к-168к/год
$110к$150кмедиана$180к
По похожим ролям (48) ~ $150к/год
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Текст:
Hirify AI/Оригинал
TL;DR
LC/MS Applications Scientist (Biocolumns): Developing HPLC and LC/MS workflows for biopharmaceutical sample preparation, method development, and data analysis with an accent on peptide, oligonucleotide, and protein therapeutics. Focus on designing reproducible experiments, generating application notes and competitive data, and providing technical support for customers and field teams.
Location: US-DE-Wilmington; based at the Little Falls, Delaware facility with an onsite presence required four days per week. Travel required up to 10% of the time.
Salary: $107,440–$167,875 per year, plus eligibility for bonus, stock, and benefits.
Company
hirify.global provides life science, diagnostic, and applied market laboratories with instruments, services, consumables, applications, and expertise.
What you will do
Develop HPLC workflows supporting biopharmaceutical sample preparation, method development, and data analysis.
Design and execute experiments for reproducible and robust workflows involving peptide, oligonucleotide, and protein therapeutics.
Support new product and workflow methodology development with the Biopharma product management and marketing teams.
Provide technical expertise through customer presentations, troubleshooting assistance, and field support.
Collaborate with Product Management, R&D, Manufacturing, and Commercial teams.
Requirements
Ph.D. degree or equivalent in chemistry, analytical chemistry, biochemistry, or a related field.
4+ years of experience with biopharmaceutical Critical Quality Attributes or purification analysis.
Experience with HPLC, LC/MS instrumentation, software, and sample preparation.
Strong knowledge of biopharmaceutical therapeutics development and characterization trends.
Ability to work independently and be self-motivated while contributing to multidisciplinary teams.
Experience and comfort with technical writing and presentations in English.
Strong communication skills and willingness to travel to conferences and customer sites.
Nice to have
Prior biopharmaceutical industry experience.
Experience with GLP-1 therapeutics, peptides, diabetes applications, injectables, or drug-product development.
Experience characterizing and testing Critical Quality Attributes.
Culture & Benefits
Collaborative and informal culture built on trust, respect, and clear accountability.
Fast-paced environment focused on biopharmaceutical solutions and customer service.
Professional development opportunities.
Full-time schedule with bonus and stock eligibility and benefits.
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