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Research Investigator

Syngene
Syngene
Fresher years
3-5 LPA
Bangalore, India
10 April 30, 2026
Job Description
Job Type: Full Time Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc. 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

Research Investigator – Analytical Research & Development (GMP Testing)

Company: Syngene International
Location: Bangalore
Department: BBRC PD ARD – GMP
Division: Dedicated Centre
Job Type: Full-Time
Experience Required: 2–6 Years Preferred | Freshers with Ph.D qualification may also be considered for entry-level research opportunities


About the Company

Syngene International is a globally recognized research, development, and manufacturing organization delivering integrated scientific services to pharmaceutical, biotechnology, nutrition, animal health, specialty chemicals, and consumer healthcare industries worldwide. Established in 1993, the company collaborates with leading global healthcare organizations including Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA, and Herbalife.

With a strong scientific workforce and innovation-driven culture, Syngene continues to accelerate drug development, improve R&D productivity, and support global pharmaceutical advancements.


Job Overview

Syngene is hiring a Research Investigator for its Analytical Research & Development (ARD) GMP division in Bangalore. The role focuses on analytical GMP testing, stability studies, method validation, instrument qualification, and regulatory-compliant laboratory operations within a cGMP-regulated environment.

This opportunity is ideal for candidates with expertise in analytical chemistry, pharmaceutical analysis, HPLC operations, dissolution studies, and GMP documentation.


Key Responsibilities

  • Perform analytical testing of drug substances and drug products for release and stability studies under GMP conditions

  • Conduct chromatographic, dissolution, and wet chemistry analysis following cGMP guidelines

  • Analyze API clinical campaign samples manufactured in pilot plant facilities

  • Handle qualification and requalification of API reference standards

  • Perform instrument calibration, qualification, troubleshooting, and maintenance

  • Execute method validation and analytical method transfer activities

  • Investigate OOS (Out of Specification), OOT (Out of Trend), and laboratory deviations

  • Prepare SOPs, validation reports, method reports, and stability summary documentation

  • Ensure compliance with quality systems, regulatory standards, and EHS guidelines

  • Maintain electronic laboratory notebooks and electronic quality management systems

  • Support laboratory operations while ensuring timely analytical result delivery


Educational Qualification

  • Ph.D in Analytical Chemistry, Pharmaceutical Sciences, Chemistry, or related Life Sciences discipline


Required Technical Skills

  • Strong theoretical and practical knowledge of analytical chemistry

  • Expertise in HPLC, dissolution apparatus, chromatographic techniques, and analytical instrumentation

  • Understanding of method validation, instrument qualification, calibration, and GMP analytical testing

  • Familiarity with ICH guidelines, cGMP regulations, and regulatory inspection standards including US FDA and MHRA

  • Experience with stability sample testing and electronic documentation systems

  • Good working knowledge of MS Office tools and laboratory documentation practices


Behavioral & Professional Skills

  • Strong attention to detail and scientific problem-solving ability

  • Excellent written and verbal communication skills

  • Ability to work efficiently in a fast-paced research environment

  • Team-oriented mindset with flexibility to work in rotational shifts

  • Strong commitment to deadlines, compliance, and laboratory excellence


Who Can Apply?

  • Experienced professionals with 2–6 years of analytical GMP laboratory experience

  • Ph.D freshers with strong analytical research exposure, thesis experience, or laboratory training may also explore this opportunity depending on project requirements


Why Join Syngene?

  • Work with one of India’s leading global CRO and CDMO organizations

  • Exposure to international regulatory standards and global pharmaceutical projects

  • Opportunity to contribute to analytical development and drug innovation programs

  • Collaborative scientific work culture with career growth opportunities in pharmaceutical R&D


Equal Opportunity Employer

Syngene International is committed to providing equal employment opportunities to all qualified individuals irrespective of gender, race, religion, disability, nationality, veteran status, sexual orientation, or any legally protected characteristic.


Keywords for Job Search

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