Specialist Scientist

JOB DESCRIPTION

Job Title: Lead Analytical Development

Job Location: Bangalore

Department: Biopharmaceutical Development

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 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

1. Overall adherence to safe practices and procedures of oneself and the teams reporting in.
2. Contributing to development of procedures practices and systems that ensures safe operations and compliance to companys integrity & quality standards.
3. Driving a corporate culture that promotes environment health and safety (EHS) mindset and operational discipline at the workplace at all times.
4. 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.
5. 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.
6. Compliance to Syngenes 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 Values

All employees will consistently demonstrate alignment with our core values

• Excellence
• Integrity
• Professionalism

Experience

Seeking 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 Capabilities

• Develop 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 reports
• Ensure compliance with ICH USP GLP/GMP and data integrity standards.
• Collaborate with QA QC and cross-functional teams.

Education

• Masters degree in Life Science Chemical Engineering Biotechnology or related field.

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 addition Syngene will provide reasonable accommodations for qualified individuals with disabilities.