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Senior Research Associate

1-5 years
Not Disclosed
10 Nov. 25, 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 (Hyderabad, India)

Location: Mallapur, Hyderabad
Department: Chemistry Solutions
Employment Type: Full-Time

Overview

We are seeking a highly skilled Senior Research Associate to support advanced chemical synthesis projects for global clients. This role involves executing complex chemical reactions, developing high-quality compounds, and ensuring adherence to scientific, safety, and data-integrity standards. The ideal candidate will have strong expertise in organic synthesis and hands-on laboratory experience.

Role Scope

The position requires performing chemical reactions to synthesize targeted molecules and compounds as per client expectations. You will be responsible for running experiments using efficient routes, validated techniques, and optimized resource utilization.


Key Responsibilities

1. Execute Chemical Reactions and Synthesis Activities

  • Understand project objectives, client requirements, and proposed synthetic routes.

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

  • Identify potential safety hazards and implement mitigation measures under supervisor guidance.

  • Plan and perform chemical reactions using appropriate reagents, equipment, and controlled parameters such as temperature and pressure.

  • Manage multiple reactions in parallel while ensuring efficiency and accuracy.

  • Monitor reaction progress using analytical techniques and document findings.

  • Conduct workup and purification processes to obtain intermediates or final compounds at required purity levels.

  • Analyze analytical data, interpret results, and prepare detailed synthesis reports.

  • Achieve productivity expectations aligned with reaction count, steps, compound quality, purity, and project timelines.

2. Maintain Laboratory Safety and Quality Standards

  • Follow Good Laboratory Practices (GLP) and ensure strict compliance with all safety protocols.

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

  • Maintain clean and organized laboratory workspaces in accordance with SOPs.

3. Ensure Accurate Documentation and Data Integrity

  • Record all experimental procedures, reactions, observations, and results in laboratory notebooks as per client documentation guidelines.

  • Maintain strict confidentiality of intellectual property (IP).

  • Prepare final reports and ensure complete data integrity.

4. Support Knowledge Enhancement and Team Development

  • Participate in training programs, discussions with supervisors, and continuous learning sessions to enhance technical knowledge in organic/medicinal chemistry and analytical techniques.

  • Contribute to a positive and growth-oriented team environment.


Functional & Technical Skills Required

  • Strong knowledge of Organic/Medicinal Chemistry and synthetic execution.

  • Proficiency in laboratory safety systems and protocols.

  • Understanding of data integrity, IP protection, and confidentiality standards.

  • Ability to optimize resources and perform cost–benefit analysis.

  • Competence in handling analytical instruments and interpreting analytical data.


Educational Qualification & Experience Requirements

  • M.Sc. in Organic Chemistry or Medicinal Chemistry.

  • 1 to 5 years of relevant hands-on experience in chemical synthesis, R&D, or laboratory research.

  • Candidates with research publications in reputed scientific journals will be preferred.


Additional Information

  • Reporting structure and designation will be defined internally based on project allocation.

  • Industry experience in pharmaceuticals, chemical research, or CRO environments is desirable.

  • Strong documentation skills and adherence to quality systems are essential.