Senior Executive

As an Executive or Senior Executive at Syngene, your primary responsibility will be method development, validation, and stability testing of drug substance/drug product. You should have strong hands-on experience in developing and validating Assay & related substances methods for drug substance/drug product. Additionally, you should be willing to work with complex injectables and be open to working in shifts. - Handle instruments such as HPLC, UPLC, GC, UV Visible spectrophotometer, balances, Potentiometer, and stability chambers. - Well-versed in Good documentation/laboratory practices like ALCOA+. - Experience in calibration and qualification of laboratory instruments. - Prepare and review raw data sheets, instrument operating procedures, and standard operating procedures. In this role, you will also be accountable for procurement and inventory maintenance of Pharmacopeial Standards/Chemicals/Reagents/Consumables/Spares required for projects. Adherence to GxP/Safety procedures and internal standard operation procedures is crucial. Proficiency in operating MS Office tools and effective communication skills are essential for interactions with clients and external users. To excel in this position, you should possess good interpersonal skills, self-time management abilities, and be a strong team player. The role also requires polite and effective communication skills. Syngene Values: At Syngene, the values of Excellence, Integrity, and Professionalism are upheld, and as a team member, you are expected to consistently demonstrate alignment with these core values. Specific Requirements: - Experience: 3-6 years - Skills And Capabilities: Hands-on experience in HPLC, UPLC/UHPLC, GC, UV-Visible spectrophotometer, Potentiometer, and other analytical instruments. Knowledge of good documentation/laboratory practices such as ALCOA+ is required. Experience in particle size determination, Zeta potential, and particulate matter analysis techniques will be advantageous. Familiarity with SEC, CGE methods for mAbs is a plus. Proficiency in MS Office tools is necessary. - Education: M. Pharm /M. Sc with 3-6 years" experience in R&D under GMP environment (QC),