Job Title: Research Investigator – Pathology / Immunohistochemistry (IHC)
Company: Syngene International Ltd.
Location: Bangalore, Karnataka, India
Department: Pathology / Immunohistochemistry (IHC)
Division: Dedicated Centre
Job Type: Full-Time
Experience Required: 2–5 Years of Experience in Histopathology, Immunohistochemistry (IHC), or Translational Research
About Syngene International
Syngene International Ltd., established in 1993, is a global contract research, development, and manufacturing organization (CRDMO) that provides integrated scientific services to pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries worldwide.
Syngene collaborates with global industry leaders including Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA, and Herbalife. With a strong team of research scientists and experts, the organization focuses on solving complex scientific challenges, improving research productivity, accelerating time to market, and optimizing the cost of innovation.
Role Overview
The Research Investigator – Pathology / IHC will support translational research programs by leading immunohistochemistry (IHC) and pathology-based biomarker assay development, validation, and analysis. This role works closely with pathologists, scientists, and research teams to support clinical biomarker programs and pathology workflows.
The position involves collaboration with internal research teams and hospital networks to support translational pathology studies and ensure accurate analysis of clinical samples in regulated research environments.
Key Responsibilities
Clinical Pathology and Translational Research Support
Provide clinical pathology support for research programs and projects in collaboration with internal and partner pathology teams.
Work closely with pathologists and research scientists to support translational research initiatives and biomarker discovery programs.
IHC and ISH Assay Development
Develop, optimize, and validate Immunohistochemistry (IHC) and In Situ Hybridization (ISH) assays for clinical biomarker studies.
Conduct sample processing, assay validation, and analysis of research and clinical samples.
Digital Pathology Workflow Support
Support digital pathology workflows and analysis under the supervision of senior pathologists.
Participate in training and development activities related to digital pathology technologies.
Research Collaboration and Program Support
Collaborate with hospital networks and clinical research teams to support translational R&D projects.
Assist in integrating pathology data into clinical development programs and research initiatives.
Laboratory Documentation and SOP Management
Participate in the preparation, review, and maintenance of Standard Operating Procedures (SOPs).
Ensure laboratory documentation is accurate and maintained in accordance with regulatory and quality standards.
Inventory and Laboratory Resource Management
Support inventory management for laboratory reagents, consumables, and pathology supplies.
Ensure efficient utilization of laboratory resources and timely availability of materials required for research activities.
Data Quality and Research Integrity
Ensure experiments are conducted accurately and generate reproducible scientific data.
Maintain proper documentation and quality control processes within the laboratory environment.
Educational Qualifications
MBBS with MD or DNB in Pathology.
Experience Requirements
2–5 years of experience in histopathology, immunohistochemistry (IHC), or translational research environments.
Experience working in hospital pathology laboratories, research institutes, or pharmaceutical research organizations is preferred.
Technical Skills
Pathology and Histopathology Expertise
Hands-on experience in pathology and histopathological analysis within hospital or research environments.
Immunohistochemistry (IHC) Techniques
Strong practical experience in IHC assay development, optimization, and sample analysis.
Digital Pathology Knowledge
Basic knowledge or exposure to digital pathology systems and workflows is desirable.
Clinical Sample Handling
Experience working with clinical samples and supporting clinical research or biomarker development programs.
Regulatory Laboratory Environment
Experience working in regulated laboratory environments such as CAP, NABL, or other GxP-compliant facilities is advantageous.
Behavioral Competencies
Strong attention to detail and commitment to research accuracy.
Excellent written and verbal communication skills.
Ability to collaborate effectively in multidisciplinary research teams.
Strong analytical and problem-solving capabilities.
Equal Opportunity Employer
Syngene International Ltd. is committed to providing equal employment opportunities to all qualified candidates regardless of race, gender, religion, nationality, disability, or other protected characteristics. The organization promotes diversity, inclusion, and fair employment practices and provides reasonable accommodations for individuals with disabilities in accordance with applicable laws.
Job Location
Bangalore, Karnataka, India.
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