Syngene Analytical Scientist Job For Pharma – Apply Online
Title: Junior Analytical Development Scientist
Date: 28 Nov 2024
Job Location: Bangalore
Department: Analytical Development – Drug Product
About Syngene:
Syngene is an innovation-led contract research, development, and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the core of personal and professional operations, with shared responsibility for compliance with safety guidelines, procedures, and SOPs.
Mandatory Expectations for All Roles as per Syngene Safety Guidelines:
- Overall adherence to safe practices and procedures by oneself and aligned teams.
- Contribution to the development of procedures, practices, and systems ensuring safe operations and compliance with company integrity and quality standards.
- Promotion of a corporate culture focused on Environment, Health, and Safety (EHS) and operational discipline at the workplace.
- Ensuring safety by adhering to safety protocols and meeting EHS requirements at all times.
- Completion of all assigned mandatory trainings related to data integrity, health, and safety measures on time.
- Compliance with Syngene’s quality standards at all times.
Core Purpose of the Role:
- Support analytical development for formulation development.
- Perform routine sample analysis.
- Conduct method development and instrument calibrations.
- Prepare documentation and reports.
- Manage miscellaneous lab responsibilities.
Role Accountabilities:
- Strong educational and theoretical background.
- Knowledge of calibration, method development, and troubleshooting using instruments like:
- Analytical instruments: Zetasizer, Mastersizer, Osmometer, KF Auto Titrator, dissolution apparatus (I, II & IV).
- Spectroscopic instruments: UV spectrometer, IR.
- Chromatographic instruments: HPLC/UPLC, GC, Liquid Particulate Counter.
- Familiarity with regulatory guidelines for method development, product development, and documentation.
- Proficiency in method development for injectable formulations, including:
- Tests for assay, degradation products, dissolution, content uniformity.
- Cleaning methods and degradation products for liposomes/microspheres.
- Free and bound API assay.
- Knowledge of specification setting for parenteral dosage forms and in-process/finished product specifications.
- Experience with instruments like LC-MS, GC-MS is an added advantage.
- Understanding of GxP-compliant documentation, including:
- Online lab notebook writing (e.g., ELN).
- Method development reports, test reports, SOP preparation, calibration documentation.
- Review of documents generated by peers or juniors.
- Ability to search scientific literature online.
Syngene Values:
Employees must consistently demonstrate alignment with Syngene’s core values:
- Excellence
- Integrity
- Professionalism
Experience: 3–7 years of relevant experience.
Skills and Capabilities:
Technical/Functional Skills:
- Proficiency in MS Office tools.
- Ability to search scientific literature online.
Behavioral Skills:
- Strong commitment to work with a high level of dedication, enthusiasm, and motivation.
- Good communication skills (speaking, listening, writing) with attention to detail.
- Proactive and able to work in dynamic, ambiguous environments.
- Ability to meet tight deadlines and develop creative solutions.
- Team-oriented and flexible to work in shifts.
Education: M.Pharm / M.Sc.
Apply for this position here
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