Senior Executive 12/08/2025

JOB DESCRIPTION Job Role Analytical Chemistry-Analyst Department Analytical - BGRC Job Location Bangalore 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 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 lab plant 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 Core Purpose of the Role This role involves method development method validation method transfer and R D stability studies by using laboratory instruments like Ultra performance liquid chromatography UPLC High Performance Liquid Chromatography HPLC Gas Chromatography GC Ultraviolet UV spectrophotometer Polarimeter etc Role Accountabilities Must have strong hands-on experience in development and validation of Assay related substances methods for drug substance drug product Managing the stability studies for individual projects and stability data analysis knowledge on stability guidelines and maintaining the sample storage Must have experience in handling HPLC UPLC Empower-3 software GC UV Visible spectrophotometer balances Potentiometer and stability chambers Shall have experience on Good documentation laboratory practices such as ALCOA Experience in calibration and qualification of HPLC UPLC GC and other QC laboratory instruments Shall prepare and review the raw data sheets instrument operating procedures and standard operating procedures Shall have good experience in handling of QMS such as incidents Out of Specifications Deviations and Change control Shall be responsible for procurement and inventory maintenance of Pharmacopeial Standards Chemicals Reagents Consumables Spares etc required for the projects Shall adhere to the procedure of GxP Safety and as per the procedure defined in the internal standard operation procedure Shall operate the MS office word excel ppt outlook and other essential tools required for routine activity Good communication and e-mail writing skills are required since the candidate needs to communicate to client external users situated overseas Behavioral Skills Good Interpersonal skills Self-time management Good Team player Polite Good Communication skills Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Experience 3-6 years Skills and Capabilities Hands-on HPLC UPLC UHPLC CG UV-Visible spectrophotometer Potentiometer and QC other analytical instruments Theoretical knowledge in Chromatography and spectroscopy technique Good documentation laboratory practices such as ALCOA Able to follow work instructions and perform the tasks under the supervision of the Team leader Preparation and Maintenance of all the documents Good knowledge of MS-office word excel ppt