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Senior Research Associate

Aragen
Aragen
1-5 years
preferred by company
10 Dec. 20, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Research Associate – Chemistry Solutions

Location: Hyderabad, India
Office Location: Mallapur, Hyderabad
Department: Chemistry Solutions
Job Type: Full-Time | On-site
Experience Required: 1–5 Years
Salary Range: Competitive (Annual, INR – as per experience and skill level)


Job Overview

We are seeking a Senior Research Associate – Chemistry Solutions to support chemical synthesis projects by executing laboratory reactions and delivering high-quality compounds aligned with client specifications. This role is ideal for professionals with hands-on experience in organic or medicinal chemistry, who are passionate about laboratory research, safety compliance, and data integrity.

The position involves independent reaction execution, analytical monitoring, purification, documentation, and collaboration within a safety-driven laboratory environment.


Key Responsibilities

Chemical Synthesis and Reaction Execution

  • Execute chemical reactions to synthesize target molecules and compounds as per defined project requirements and synthetic routes.

  • Interpret client specifications and understand reaction pathways and deliverables.

  • Plan and perform reactions using appropriate reagents, solvents, glassware, and laboratory equipment under controlled conditions (temperature, pressure, time).

  • Ensure parallel execution of multiple reactions while optimizing resource utilization and minimizing waste.

Safety and Laboratory Compliance

  • Review and discuss Material Safety Data Sheets (MSDS) with team members prior to execution.

  • Identify potential safety risks and implement mitigation strategies in coordination with supervisors.

  • Follow Good Laboratory Practices (GLP), safety protocols, and laboratory SOPs at all times.

  • Ensure proper use, maintenance, and housekeeping of laboratory instruments and equipment.

Analytical Monitoring and Data Interpretation

  • Monitor reaction progress using appropriate analytical techniques.

  • Perform work-up and purification using suitable techniques to achieve desired purity and quality standards.

  • Analyze analytical data, evaluate results, and interpret synthesis outcomes accurately.

  • Meet defined productivity benchmarks related to number of reactions, steps, compounds, purity, and timelines.

Documentation, Data Integrity, and IP Protection

  • Maintain accurate and complete laboratory notebooks and records in compliance with client and organizational requirements.

  • Ensure data integrity, traceability, and strict intellectual property confidentiality.

  • Prepare technical summaries and final reports as required.

Continuous Learning and Skill Development

  • Enhance knowledge in organic synthesis, medicinal chemistry, and analytical techniques through mentoring, training programs, and ongoing education.

  • Actively participate in project discussions, classroom training, and skill development initiatives.


Required Qualifications and Experience

Education

  • MSc in Organic Chemistry or Medicinal Chemistry

Experience

  • 1–5 years of relevant laboratory experience in chemical synthesis, CROs, pharmaceutical R&D, or chemical research organizations


Preferred Qualifications

  • Research publications in reputed or peer-reviewed scientific journals

  • Exposure to cost-benefit analysis and efficient resource utilization in laboratory settings


Key Skills and Competencies

  • Strong knowledge of organic and medicinal chemistry synthesis

  • Hands-on experience with laboratory equipment and analytical techniques

  • Thorough understanding of laboratory safety protocols and GLP

  • Knowledge of IP protection, confidentiality, and data integrity standards

  • Ability to plan, execute, and document experiments independently

  • Strong analytical thinking, attention to detail, and problem-solving skills

  • Ability to work collaboratively while managing multiple reactions and timelines


Work Environment

  • On-site laboratory role in a controlled research environment

  • Requires adherence to safety, documentation, and quality systems

  • No routine travel required unless specified by project needs


Why This Role

  • Opportunity to work on client-driven chemical synthesis projects

  • Exposure to diverse molecules and synthetic techniques

  • Strong foundation for career growth in pharmaceutical R&D and chemistry solutions

  • Structured learning environment with emphasis on safety, quality, and innovation


SEO Keywords for Global Reach

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