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RK PHARMA Verified
Pharmaceutical Manufacturing, Biotechnology Research

Analytical Scientist / Senior Analytical Scientist

Pearl River, NYOnsiteFull TimeSenior$70,000–$90,000 /yrPosted 2 months agoVisa sponsorship available

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Required skills

  • Analytical Scientist
  • Senior Analytical Scientist
  • Chemistry
  • Analytical Chemistry
  • Pharmaceutical Sciences
  • Pharmacy
  • HPLC
  • UPLC
  • GC
  • UV-Visible Spectroscopy

Nice to have

  • injectable products
  • oral liquid products
  • SAP
  • Microsoft Office Suite
  • OOS
  • OOT

Role summary

RK Pharma is seeking an Analytical Scientist or Senior Analytical Scientist to support analytical development, validation, testing, and product lifecycle activities within pharmaceutical programs. This role collaborates with cross-functional teams including Formulation Development, Quality Assurance, Regulatory Affairs, Manufacturing, and Quality Control to ensure analytical methods and data meet scientific and regulatory standards. Responsibilities include developing and validating methods using various instrumentation (HPLC, UPLC, GC, etc.), performing analytical testing, executing stability studies, and supporting investigations. Experience with cGMP, ICH guidelines, and software like Empower 3 is essential. The level of hire depends on experience, with 5+ years required for Analytical Scientist and 8-12+ years for Senior Analytical Scientist.

Description

About RK Pharma

RK Pharma is a pharmaceutical organization focused on developing and manufacturing high-quality, affordable drug products through disciplined execution and strong internal collaboration. Our teams work across development, quality, manufacturing, and regulatory functions to bring products from concept to commercialization while maintaining the standards expected in regulated pharmaceutical environments. We value people who are thoughtful, scientifically curious, and committed to doing careful work.

About the Role

The Analytical Scientist / Senior Analytical Scientist supports analytical development, validation, testing, and product lifecycle activities across a variety of pharmaceutical programs. This role works closely with Formulation Development, Quality Assurance, Regulatory Affairs, Manufacturing, and Quality Control to ensure analytical methods and laboratory data meet scientific and regulatory expectations. The level of hire will be based on experience and demonstrated expertise.

Key Responsibilities

  • Develop, optimize, validate, and transfer analytical methods for assay, related substances, dissolution, cleaning validation, and stability testing.
  • Support method verification, transfers, and lifecycle management.
  • Perform analytical testing of APIs, raw materials, in-process samples, finished products, and stability samples.
  • Execute testing using HPLC, UPLC, GC, UV-Visible Spectroscopy, FTIR, dissolution systems, and particle size analysis instrumentation. Support formulation and development projects through analytical testing and scientific collaboration.
  • Execute and monitor stability studies. Prepare and review SOPs, specifications, protocols, reports, and laboratory documentation.
  • Support investigations involving OOS, OOT, deviations, CAPAs, and change controls.
  • Operate, maintain, calibrate, and troubleshoot laboratory instrumentation.
  • Collaborate with Regulatory Affairs, Quality Assurance, Manufacturing, and Development teams.
  • Mentor junior analysts and support training activities where appropriate.

What We’re Looking For

Required

  • Bachelor's degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Pharmacy, or a related scientific discipline. Master's degree preferred.
  • Analytical Scientist: approximately 5+ years of pharmaceutical laboratory experience. Senior Analytical Scientist: approximately 8–12+ years of pharmaceutical analytical development and/or quality control experience.
  • Experience supporting injectable, or oral liquid products preferred.

Technical Expertise

Strong working knowledge of :

Instrumentation

  • HPLC, UPLC, and GC systems
  • UV-Visible Spectrophotometer
  • FTIR Spectroscopy
  • Dissolution Testing (USP Apparatus I & II)
  • Particle Size Analysis (Malvern Mastersizer and Zetasizer)
  • Karl Fischer Titration
  • Brookfield Viscometer

Software

  • Empower 3
  • LabSolutions
  • SAP
  • Microsoft Office Suite

Regulatory Knowledge

  • FDA Regulations
  • ICH Guidelines
  • USP Requirements
  • cGMP
  • cGLP
  • GDP
  • Quality by Design (QbD)

How We Work

At RK Pharma, quality comes before speed. We believe strong science is built through curiosity, collaboration, and disciplined execution. People who succeed here tend to be thoughtful, dependable, scientifically curious, accountable, and comfortable working across teams.

People who succeed in this role are steady, reliable, and take pride in supporting the environment where quality work happens.

What We Offer

  • A stable and respectful work environment
  • Clear expectations and consistent routines
  • Training on procedures and safety requirements
  • The opportunity to contribute to a workplace that depends on cleanliness and care

Equal Opportunity Employer

RK Pharma is an equal opportunity employer. We are committed to fair, consistent, and respectful hiring practices.

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