4 дня назад
Scientist II, Verification Programs
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Scientist II, Verification Programs (Pharmaceutical Analytical Testing): Conducting analytical testing and preparing verification reports for dietary supplements and dietary ingredients with an accent on laboratory precision, pharmaceutical quality standards, and compliance. Focus on troubleshooting complex analytical issues, maintaining calibrated equipment, supporting ISO audits, and applying HPLC, dissolution, and other laboratory techniques.
Location: Hyderabad, India
Salary: Not specified
Company
is an independent scientific nonprofit organization that develops public quality standards and programs for medicines, dietary supplements, and food ingredients.
What you will do
- Conduct verification projects for dietary supplements and dietary ingredients using assigned analytical methods.
- Complete laboratory projects on schedule and perform testing and data analysis accurately.
- Prepare project reports, respond to QA observations, and support internal and external audits.
- Troubleshoot technical laboratory issues and propose improvements to laboratory operations.
- Maintain equipment calibration, laboratory safety, GLP compliance, and required supplies.
- Support analytical testing and review activities for public health, reference standards, and other departmental programs.
Requirements
- Master’s degree in pharmacy or analytical chemistry.
- 3–6 years of relevant laboratory experience, preferably in pharmaceutical manufacturing QC or contract analytical testing.
- Experience with pharmaceutical dosage forms, including oral and liquid products.
- Strong HPLC and Empower software experience, plus proficiency in dissolution analysis.
- Strong written and verbal communication, technical analysis, and independent troubleshooting skills.
- Ability to follow GLP, safety, quality, and pharmaceutical testing requirements.
Nice to have
- Experience with GC, ICP-OES, ICP-MS, LC-MS, IR, Karl Fischer, UV, ion chromatography, disintegration, and wet chemical analysis.
- Knowledge of USP, BP, EP, ICH, FDA regulations, compendial procedures, and customer-specific methods.
- Experience with ELN systems, QMS, ISO/IEC 17025, ISO 9001, and regulatory audits.
Culture & Benefits
- Mission-driven work focused on improving access to safe, high-quality medicines and supplements.
- Inclusive environment with opportunities for mentorship and professional development.
- Company-paid time off, healthcare options, and retirement savings benefits.
- Collaboration with scientific, technical, public health, industry, academic, healthcare, and government experts.
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