Senior Research Associate

2 weeks ago

Navi Mumbai, Maharashtra, India Fusion Scientific Laboratories Full time ₹ 6,00,000 - ₹ 18,00,000 per year

Location: Rabale, Navi Mumbai

Experience: 2 to 7 years

Industry: Pharmaceutical / Analytical Research

Department: Analytical Research and Development (AR&D)

Employment Type: Full-time

About Us

Fusion Scientific Laboratories is a globally recognized, USFDA and EMA accredited pharmaceutical laboratory located in Rabale, Navi Mumbai. We specialize in Formulation Development, Analytical Solutions, and Integrated Pharmaceutical Services (CDMO). Our commitment to innovation, quality, and regulatory excellence positions us as a trusted partner to leading pharmaceutical companies around the world.

Position Overview

We are seeking dynamic and detail-oriented professionals for the role of Senior Research Analyst, Executive, or Senior Executive in our Analytical Development team. The ideal candidate will have 2 to 7 years of hands-on experience in using advanced analytical instrumentation including ICP-MS, Ion Chromatography, GC, and GC-MS. The role involves developing and validating analytical methods, performing batch analysis, and supporting the overall analytical strategy for drug substances and drug products.

Key Responsibilities

  • Analytical Method Development for drug substances and drug products using ICP-MS, Ion Chromatography, GC and GC-MS.
  • Analytical Method Validation in compliance with regulatory guidelines (ICH, USFDA, EMA).
  • Routine and Stability Sample Analysis using validated methods to support formulation and process development.
  • Perform instrument calibration, maintenance, and troubleshooting to ensure smooth lab operations.
  • Prepare protocols, method development reports, validation reports, and SOPs as per regulatory standards.
  • Conduct investigations, deviations, and ensure proper data integrity and documentation in line with GMP/GLP guidelines.
  • Collaborate with cross-functional teams including Formulation, QA, and Regulatory Affairs for project deliverables.
  • Ensure compliance with cGMP, GLP, and regulatory audit requirements.

Required Skills & Qualifications

  • Masters degree in Pharmaceutical Sciences, Analytical Chemistry, or related field.
  • 2 to 7 years of relevant industry experience in pharmaceutical analytical development.
  • Proficient in handling and troubleshooting ICP-MS, Ion Chromatography, GC, and GC-MS instruments.
  • Strong understanding of regulatory guidelines (ICH, USFDA, EMA) related to analytical method development and validation.
  • Experience in batch analysis of pharmaceutical products.
  • Knowledge of GMP/GLP practices, data integrity, and regulatory documentation.
  • Ability to manage multiple projects with attention to detail and accuracy.
  • Excellent verbal and written communication skills.

Why Join Us

  • Be part of a fast-growing, globally accredited laboratory setting benchmarks in pharmaceutical services.
  • Work with cutting-edge technologies and industry experts.
  • Opportunities for professional growth and skill development.
  • Competitive salary and performance-based incentives.

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