Pharmaceutical Jobs at Syngene | Apply Now for the Formulation Scientist Position
Syngene International, a leading innovation-driven contract research and manufacturing organization, is hiring a Formulation Scientist (Parenteral) in Bangalore. This role focuses on formulation development, technology transfer, and process optimization for injectable drug products, ensuring successful clinical and commercial supply. If you are passionate about pharmaceutical R&D and want to contribute to global healthcare, this opportunity is designed for you.
- Job Title: Formulation Scientist (Parenteral)
- Location: Syngene International, Bangalore
About Syngene:
Syngene is a global, innovation-led contract research, development, and manufacturing organization. We provide integrated scientific services from discovery to commercial supply. At Syngene, safety, integrity, and quality are at the core of everything we do.
Core Purpose of the Role:
The role involves the formulation development of parenteral drug products, including pre-formulation, formulation design, process optimization, and technology transfer from R&D to GMP manufacturing. The scientist will lead scale-up and clinical trial drug supply, ensuring compliance with global regulatory standards.
Responsibilities:
- Develop formulations for parenteral drug products (small and large molecules).
- Lead technology transfer to GMP manufacturing sites.
- Optimize processes for first-time-right manufacturing.
- Support clinical trial supplies and troubleshoot technical, clinical, and registration batches.
- Collaborate with production, quality, and third-party facilities.
- Prepare and review technical reports, GMP documents, and proposals.
Skills & Capabilities:
- Strong expertise in injectable drug formulation (conventional and complex, e.g., liposomes, nanoemulsions, nanoparticles, lyophilized products).
- Knowledge of packaging formats (vials, PFS, autoinjectors) and regulatory requirements for USA/EU.
- Experience in analytical characterization, biosimilars, process validation, and troubleshooting.
- Hands-on GMP experience with strict adherence to data integrity and compliance.
- Familiarity with QMS, deviations, OOT, OOS, and CAPA.
- Prior exposure to regulatory filings and audits (US, EU, ROW).
- Strong collaboration and communication skills for cross-functional team interaction.
Qualifications & Experience:
- Master’s degree in Pharmacy (Pharmaceutics/Industrial Pharmacy/Process Technology).
- Minimum 3 years of industry experience in formulation development and technology transfer of parenteral products.
Why Join Syngene?
At Syngene, you will work in a collaborative and innovation-driven environment, contributing to healthcare advancements globally. We are committed to safety, professional growth, and equal opportunities.
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