Principal Scientist - Analytical Development

Date: 26 Aug 2026
Location:
Bangalore, KA, IN, 560099
Division: Development Services
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
Maintain cleanliness of lab and instrumentation area
Overall adherence to safe practices and procedures of oneself and the teams aligned
Compliance to Syngene’ s quality standards always
Method development and validation
Follow the GDP for documents
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: 10 - 15 years
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.

Work arrangement
No