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Assistant Manager

Syngene
Syngene
8-12 years
Not Disclosed
10 Jan. 6, 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

Assistant Manager / Project Leader – Small Molecule Bioanalytical Laboratory | Bengaluru, India

Company: Syngene International Limited
Location: Bengaluru, Karnataka, India
Division: Discovery Services – Clinical Development
Experience Required: 8–12 years in bioanalytical research
Job Type: Full-Time, On-Site


About Syngene

Syngene International Ltd. (BSE: 539268, NSE: SYNGENE) is a leading integrated research, development, and manufacturing organization, offering global scientific services to pharmaceuticals, biotechnology, nutrition, animal health, consumer goods, and specialty chemicals sectors.

With 4500+ scientists and 1.9 million sq. ft. of dedicated discovery and manufacturing facilities, Syngene delivers high-quality science, robust data management, and IP security, enabling faster time-to-market and cost-effective innovation. Our clients include global leaders such as Amgen, Baxter, Bristol-Myers Squibb, Herbalife, GSK, and Merck KGaA.


Role Overview

The Assistant Manager / Project Leader in the Small Molecule Bioanalytical Laboratory will provide technical leadership and oversight for bioanalytical studies, including method development, validation, and study sample analysis. The role ensures regulatory compliance, scientific excellence, and high-quality deliverables across projects.

This position reports to the Group Leader, Small Molecule Bioanalytical Laboratory and is based in Bengaluru, India. The ideal candidate will combine scientific expertise in small molecule bioanalysis with team leadership skills to guide high-performing teams, troubleshoot complex studies, and ensure timely delivery of results.


Key Responsibilities

Scientific & Technical Leadership:

  • Perform and oversee bioanalytical method development, method validation, and sample analysis according to SOPs, STPs, and study protocols.

  • Review analytical data, entries, and results to ensure accuracy and compliance.

  • Lead technical troubleshooting and provide guidance to Scientists and Research Associates.

  • Ensure adherence to regulatory guidelines (GLP/GCP) and quality standards in all studies.

Project & Team Management:

  • Lead project discussions, coordinate resources, and ensure timely completion of assigned deliverables.

  • Foster a culture of excellence, mentoring team members, conducting performance assessments, and developing team competencies.

  • Collaborate with QA and documentation teams for report preparation, audits, and regulatory inspections.

Operational Excellence & Compliance:

  • Coordinate with maintenance teams for instrument/equipment troubleshooting (LC-MS/MS, HPLC, etc.).

  • Ensure all bioanalytical experiments meet ALCOA++ standards for documentation and data integrity.

  • Participate in risk mitigation planning and continuous process improvement initiatives.


Qualifications & Experience

  • Education: Master’s or Ph.D. in Pharmaceutics, Pharmaceutical Sciences, or related Life Sciences.

  • Industry Experience: 8–12 years in small molecule bioanalytical research, with hands-on expertise in regulated bioanalytical experiments.

  • Leadership Experience: Proven experience in managing and mentoring high-performing bioanalytical teams.

  • CRO Experience: Prior experience in a bioanalytical CRO environment is advantageous.


Core Competencies

Scientific Expertise:

  • Strong analytical thinking, innovative problem-solving, and scientific curiosity.

  • In-depth understanding of drug mechanisms, patient populations, and assay strategies.

Technical Skills:

  • Hands-on experience with LC-MS/MS, HPLC, and other analytical instruments.

  • Expertise in method development, validation, and regulatory-compliant bioanalytical processes.

  • Effective project management, client engagement, and risk mitigation skills.

Documentation & Communication:

  • Strong command of English (written and oral) for report writing and presentations.

  • High attention to detail in data recording, documentation, and compliance.


Equal Opportunity Employer

Syngene is committed to equal employment opportunity (EEO) and provides reasonable accommodations for qualified individuals with disabilities. We welcome applications regardless of age, color, nationality, disability, gender, religion, or any other legally protected characteristic.


Apply Now to lead cutting-edge small molecule bioanalytical research and contribute to Syngene’s mission of accelerating global pharmaceutical innovation.