Syngene Jobs For MPharm Graduates | Apply Now For The Senior Executive Role
Syngene is hiring a Senior Executive in Bangalore to join its dynamic R&D team. This role is ideal for professionals with 3–6 years of experience in the development, validation, and stability testing of analytical methods for drug substances and products. If you have hands-on expertise in HPLC, UPLC, GC, UV-Visible spectrophotometry, and QC instruments, this is an excellent opportunity to grow your career with a leading global contract research organization.
- Job Position: Senior Executive
- Location: Bangalore, Karnataka, India
About the Company:
Syngene International Ltd. is an innovation-led contract research, development, and manufacturing organization that provides integrated scientific services from early discovery to commercial supply. Syngene emphasizes safety, quality, and integrity, fostering a collaborative culture for scientific innovation and professional growth.
Job Description:
The Senior Executive will be responsible for developing, validating, and testing the stability of drug substances and products. This role requires hands-on experience with complex injectables and working knowledge of QC laboratory instruments. The candidate will ensure compliance with GxP, safety, and quality standards, while supporting efficient R&D operations. Shift flexibility is required.
Key Responsibilities:
- Develop and validate methods for assay and related substances for the drug substance/product.
- Operate and maintain analytical instruments, including HPLC, UPLC (Empower-3), GC, UV-Visible spectrophotometer, potentiometer, and stability chambers.
- Follow ALCOA+ documentation and laboratory practices.
- Calibrate and qualify HPLC, UPLC, GC, and other QC laboratory instruments.
- Prepare and review raw data sheets, instrument SOPs, and standard operating procedures.
- Handle QMS processes, including incidents, OOS, deviations, and change control.
- Procure and maintain inventory of pharmacopeial standards, chemicals, reagents, consumables, and spares.
- Adhere to GxP, safety, and internal SOP procedures.
- Operate MS Office (Word, Excel, PowerPoint) and Outlook for daily tasks and communication.
- Communicate effectively with clients and external stakeholders.
- Develop and validate SEC, CGE methods, especially for monoclonal antibodies (mAbs).
Qualifications:
- Education: M. Pharm or M.Sc with 3–6 years of experience in R&D under a GMP/QC environment.
- Hands-on experience with HPLC, UPLC/UHPLC, GC, UV-Visible spectrophotometer, potentiometer, and other QC analytical instruments.
- Strong knowledge of documentation/laboratory practices (ALCOA+).
- Experience with particle size determination, zeta potential, and particulate matter analysis is an advantage.
- Experience in developing and validating SEC, CGE methods for mAbs is preferred.
- Proficient in MS Office (Word, Excel, PowerPoint).
- Strong interpersonal, communication, and teamwork skills.
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