Principal Scientist Analytical Development

Job Title: Principal Scientist – Analytical Development

Department: Drug Substance Development and Manufacturing (Analytical Development)

Location: Bengaluru, India

About Syngene:  Syngene (www.syngeneintl.com) 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 heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and sops, in letter and spirit

Mandatory expectation for all roles as per Syngene safety guidelines

• Overall adherence to safe practices and procedures of oneself and the teams aligned.


• Contributing to development of procedures, practices and systems that ensure safe operations and compliance to company’s integrity & quality standards.


• Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times.


• Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements always in the workplace.


• Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self


• Compliance to Syngene’s quality standards at all times


• Hold self and their teams accountable for the achievement of safety goals.


• Govern and Review safety metrics from time to time.

Key Responsibilities:

• Managing a team of analytical Scientist


• Perform analytical actitivies using instruments like HPLC, GC, LCMS, GPC,NMR


• Overall adherence to safe practices and procedures of oneself and the teams aligned


• Routine Sample analysis using HPLC, GC, LCMS and Moisture content.


• Method development and validation


• Calibration of analytical instruments.


• Follow the GDP for documents


• To perform the daily calibrations of analytical instruments and equipment, based on need basis.


• Drive continuous improvement initiatives in analytical workflows.


• Collaborate cross-functionally with process development, quality, and manufacturing teams.

Desired Attributes:

• Strong expertise in chromatographic (HPLC, UPLC, GC), spectroscopic (NMR, MS, UV, IR), and other analytical techniques.


• Knowledge on ICH, GMP, GLP and global regulatory guidelines.


• Experience supporting drug substance development from early phase to commercial manufacturing.

Experience: Expert

Qualification – M.Sc. Chemistry 

 Equal Opportunity Employer:

It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.