Specialist Scientist - Analytical Development Biologics

Syngene International Limited; Bengaluru; On-site; INR 900,000 - 1,300,000; Full time

Benefits offered by this job

Equal Employment Opportunity

Job summary

Syngene International Limited is seeking a Specialist Scientist in Analytical Development to drive LC method development and CE-based analyses for biologics in a CDMO setting. The role focuses on lifecycle management, qualification, validation and transfer of analytical methods.

The candidate will support formulation, process development and stability studies, ensuring adherence to ICH, USP, GLP/GMP, and data integrity standards while collaborating with QA, QC, and cross-functional teams.

Qualifications

• Master’s degree in Life Science, Chemical Engineering, Biotechnology or related field.
• Hands-on experience with LC and CE techniques in biopharma/CDMO settings.
• Experience in method lifecycle management, qualification, validation and transfer.
• Knowledge of ICH, USP, GLP/GMP and data integrity standards.

Responsibilities

• Develop and optimize LC methods (SEC, IEX, HIC, RP-LC, HILIC, Pro-A) for biologics.
• Perform CE-based analyses using PA800 Plus and Maurice platforms.
• Execute method qualification, validation and transfer activities.
• Support formulation, process development and stability studies.

Skills

LC method development

CE-based analysis

Method qualification & transfer

Troubleshooting analytical methods

Documentation & reporting

Cross-functional collaboration

Education

Master’s degree in Life Science, Chemical Engineering, Biotechnology or related field

Tools

PA800 Plus

Maurice

Job description

Job DescriptionJob Title: Specialist Scientist - Analytical DevelopmentDate: 3 Nov 2026Location:Bangalore, KA, IN, 560099Division: Development ServicesJob DescriptionJob Title: Specialist Scientist - Analytical DevelopmentJob Location: BangaloreDepartment: Biopharmaceutical DevelopmentAbout 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 spiritMandatory expectation for all roles as per Syngene safety guidelinesOverall adherence to safe practices and procedures of oneself and the teams reporting in.Contributing to development of procedures, practices and systems that ensures 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 labs by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times 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.Syngene ValuesAll employees will consistently demonstrate alignment with our core valuesExcellenceIntegrityProfessionalismExperienceSeeking a skilled analytical scientist with hands-on expertise in LC and CE techniques to support biologics development in a CDMO environment. The role focuses on method lifecycle management, analytical development, qualification and transfer.Skills And CapabilitiesDevelop and optimize LC methods (SEC, IEX, HIC, RP-LC, HILIC, Pro-A).Perform CE-based analysis (CE-SDS, cIEF, CZE) using PA800 Plus/Maurice.Execute method qualification, validation, and transfer.Troubleshoot methods to improve performance and robustness.Support formulation, process development, and stability studies.Prepare analytical protocols, SOPs and reportsEnsure compliance with ICH, USP, GLP/GMP, and data integrity standards.Collaborate with QA, QC, and cross-functional teams.EducationMaster’s degree in Life Science, Chemical Engineering, Biotechnology, or related field.Equal Opportunity EmployerIt 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.