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Junior Analytical Development Scientist

3-7 years
Not Disclosed
10 Jan. 28, 2025
Job Description
Job Type: Full Time Education: B.Sc,M.Sc,B.Pharma,M.Pharma,LifeScience Graduates 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: Junior Analytical Development Scientist – Injectables
Location: Bangalore
Date Posted: 25th January 2025
Experience: 3-7 years
Department: Analytical Development – Drug Product


About Syngene

Syngene International Ltd. is an innovation-driven organization providing integrated scientific services across the pharmaceutical, biotechnology, and other industries. Syngene focuses on early discovery, development, and manufacturing services to global clients, including leading names like Bristol-Myers Squibb, Amgen, GSK, and Herbalife. The company's culture is driven by a passionate team of scientists who are committed to solving scientific problems and advancing innovation.


Job Purpose

The Junior Analytical Development Scientist will support the formulation development process for injectable drug products, focusing on routine analysis, method development, instrument calibration, documentation, and report preparation.


Key Responsibilities

  1. Routine Analysis and Method Development:

    • Conduct routine analysis of samples.
    • Develop and optimize analytical methods for injectable formulations.
    • Ensure the accuracy and precision of test results, troubleshooting issues as needed.
  2. Instrument Calibration and Maintenance:

    • Calibrate instruments and ensure proper functioning of lab equipment.
    • Maintain and troubleshoot a variety of instruments such as Zetasizer, Mastersizer, Osmometer, KF Auto Titrator, Dissolution Apparatus (I, II, IV), UV Spectrometer, IR, HPLC/UPLC, GC, and Liquid Particulate Counters.
  3. Regulatory Compliance and Documentation:

    • Ensure all activities comply with relevant regulatory guidelines (e.g., GxP).
    • Prepare method development reports (assay, degradation products, dissolution, cleaning method, etc.).
    • Write and maintain documents such as SOPs, test reports, calibration documentation, and online lab notebook entries (e.g., ELN).
  4. Knowledge and Troubleshooting:

    • Demonstrate knowledge of regulatory requirements for method and product development, including specification setting for parenteral dosage forms.
    • Troubleshoot and resolve issues with methods and instruments as needed.
    • Review documents generated by peers or junior team members.
  5. Scientific Research:

    • Search for scientific literature and apply new insights to ongoing projects.
    • Contribute to method development for injectable formulations, including tests such as assay, degradation products, content uniformity, and cleaning methods.

Essential Skills and Qualifications

  • Educational Qualification: M.Pharm, M.Sc, or similar qualifications in relevant fields.
  • Experience: 3-7 years of experience in analytical development, particularly with injectable formulations and related analytical methods.
  • Technical Skills:
    • Proficiency in instrument calibration and method development for injectable formulations.
    • Familiarity with instruments such as HPLC, UPLC, LC-MS, and GC-MS (preferred).
    • Knowledge of regulatory guidelines (e.g., GxP) for method development, product development, and documentation.
    • Strong proficiency with MS Office tools and online research.
  • Behavioral Skills:
    • Strong work ethic, dedication, and enthusiasm in team collaboration.
    • Excellent communication skills (verbal, written, and presentation).
    • Ability to work under pressure, meet deadlines, and prioritize tasks.
    • Creative problem-solving skills and a proactive approach to challenges.

Desirable Skills

  • Experience in the biotechnology or pharmaceutical industry, particularly related to injectable formulations.
  • Ability to work in shifts as required.

Equal Opportunity Employer

Syngene is committed to providing equal employment opportunities to all individuals, regardless of age, race, gender, disability, or other protected characteristics. The company also provides reasonable accommodations for individuals with disabilities.


This structured job description outlines the core responsibilities, qualifications, and skills needed for the Junior Analytical Development Scientist position, offering a clear overview for potential candidates.