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Executive

Syngene
Syngene
0-3 years
Not Disclosed
10 Jan. 19, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Job Title: Research Associate / Executive / Analyst – Small Molecule Bioanalytical Laboratory
Location: Bangalore, India
Department: Translational and Clinical Research (Small Molecule Bioanalytical Lab)
Reporting To: Project Leader / Group Leader, Small Molecule Bioanalytical Laboratory
Employment Type: Full-Time
Experience Level: 0–3 years


About Syngene

Syngene International Ltd. (BSE: 539268, NSE: SYNGENE) is a leading global integrated research, development, and manufacturing organization serving the pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries. With a team of 4,500+ scientists and state-of-the-art facilities, Syngene delivers innovative science, robust data management, and quality manufacturing to accelerate drug development and reduce time-to-market for global clients including Amgen, Baxter, Bristol-Myers Squibb, GSK, and Merck KGaA.


Role Summary

The Research Associate / Executive / Analyst will perform bioanalytical studies for small molecules, supporting BA/BE studies, method development, and validation programs. The role demands scientific rigor, technical expertise, and adherence to regulatory compliance (GCP/GLP) in all bioanalytical operations.


Key Responsibilities

  • Conduct bioanalytical experiments including sample processing, method development, method validation, and study sample analysis as per protocol and SOPs/STPs.

  • Prepare and review study protocols, method validation (MV) protocols, and sample analysis plans.

  • Document experimental results accurately in official records, ensuring ALCOA++ compliance.

  • Troubleshoot and coordinate with maintenance teams for instrument/equipment issues (e.g., LC-MS/MS, HPLC).

  • Ensure all studies adhere to regulatory standards and GCP/GLP guidelines.

  • Participate in scientific discussions, providing insights and supporting cross-functional teams.

  • Monitor risks and implement mitigation strategies in experimental work.

  • Maintain high standards in data integrity, documentation, and reporting, minimizing audit findings.


Educational Qualifications & Experience

  • Masters in Pharmaceutics or related life sciences from a reputed university.

  • Hands-on experience in regulated small molecule bioanalytical experiments.

  • Experience in a Bioanalytical CRO lab is an advantage.


Technical & Scientific Competencies

  • Expertise in LC-MS/MS, HPLC, and other bioanalytical instruments.

  • Strong knowledge of method development, method validation, and study sample analysis.

  • Ability to analyze data, troubleshoot experiments, and ensure compliance with regulatory standards.

  • Strong scientific curiosity, problem-solving skills, and project management capabilities.


Behavioral & Functional Skills

  • Detail-oriented with excellent documentation skills.

  • Strong communication and English writing skills (B+ or above).

  • Team player with collaboration, learning mindset, and initiative.

  • Ability to forecast experimental risks and implement mitigation strategies.


Why Join Syngene?

  • Work in a globally recognized bioanalytical laboratory with cutting-edge technology.

  • Be part of innovative BA/BE studies and small molecule drug development programs.

  • Collaborate with cross-functional teams on high-impact projects.

  • Gain exposure to global clients and regulatory compliance processes.

  • Opportunities for career growth, skill development, and scientific advancement.


Equal Opportunity Employer

Syngene International Ltd. is committed to equal employment opportunity (EEO). All candidates are considered regardless of age, gender, disability, religion, nationality, sexual orientation, or any legally protected characteristic. Reasonable accommodations are provided for qualified individuals with disabilities.

Learn more: www.syngeneintl.com