MPharm Job at Syngene | Apply Now for the Senior Executive Role
Syngene, a leading global CRDMO, is hiring a Senior Executive for the Analytical Chemistry – Analyst role in its Bangalore facility. This MPharm Job requires strong hands-on expertise in advanced laboratory instruments, including HPLC and UPLC (Empower-3), for method development, validation, and R&D stability studies. Ideal candidates hold a relevant M.Pharm/M.Sc. or equivalent degree and possess essential knowledge of ALCOA+ documentation practices and QMS handling (OOS, Deviations) to ensure GxP and safety compliance.
- Job Title: Senior Executive
- Location: Bangalore, KA, IN, 560099
About The Company
Syngene International Limited is an innovation-led development, and manufacturing organization (CRDMO) that provides integrated scientific services ranging from early discovery to commercial supply. Headquartered in Bangalore, India, Syngene partners with global pharmaceutical, biotechnology, nutrition, and animal health companies. The organization places paramount importance on safety, quality (GxP compliance), and integrity, with a core mission to accelerate scientific research for its clients while maintaining high ethical standards and operational discipline across all its laboratory and manufacturing activities.
Core Purpose of the Syngene Job
This role involves method development, method validation, method transfer, and R&D stability studies using laboratory instruments like Ultra Performance Liquid Chromatography (UPLC), High Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Ultraviolet (UV) spectrophotometer, Polarimeter, etc.
Accountabilities of the Syngene Job
- 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, PowerPoint), 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.
Skills and Capabilities
- Hands-on HPLC, UPLC/UHPLC, CG, UV-Visible spectrophotometer, Potentiometer, and QC other analytical instruments.
- Theoretical knowledge in Chromatography and spectroscopy techniques.
- 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, PowerPoint).
Education
- M. Pharm
