Exciting M Pharm Opportunity in Injectable Formulation R&D | Syngene Opening | Apply
Looking for a Pharma Research Job in formulation development? Syngene is hiring a Senior Scientist – DP Formulation Development (Injectable) in Bangalore. This opportunity is ideal for M Pharm professionals with experience in parenteral formulation development, process optimization, technology transfer, and GMP manufacturing. Candidates seeking a rewarding Syngene Career can gain exposure to complex injectable products, clinical trial supply, and global pharmaceutical development programs.
- Job Title: Senior Scientist – Formulation Development (Injectable)
- Job Location: Bangalore, Karnataka
About the Company
Syngene is a leading contract research, development, and manufacturing organization (CRDMO) providing integrated scientific services from early discovery through commercial supply. The company partners with global pharmaceutical and biotechnology organizations to support drug discovery, development, manufacturing, and commercialization.
Professionals pursuing a Syngene Career gain exposure to cutting-edge pharmaceutical research, advanced development technologies, global regulatory standards, and collaborative scientific innovation.
Job Description
This Pharma Research Job involves formulation and process development of parenteral drug products, technology transfer, manufacturing support, process optimization, and clinical supply activities. The selected candidate will lead injectable product development projects from pre-formulation through commercialization while ensuring compliance with GMP, quality, and safety requirements.
Key Responsibilities
- Develop parenteral and injectable drug formulations.
- Perform pre-formulation, formulation design, and process characterization.
- Lead technology transfer from R&D to manufacturing sites.
- Support GMP manufacturing and clinical trial supply.
- Optimize manufacturing processes and scale-up activities.
- Coordinate with production, quality, validation, and engineering teams.
- Prepare and review GMP documents and technical reports.
- Support regulatory submissions and audit readiness.
- Investigate deviations, OOS, OOT, and CAPA activities.
- Ensure compliance with EHS, GMP, and data integrity requirements.
Eligibility Criteria
- Education: M Pharm (Pharmaceutics, Industrial Pharmacy, or Process Technology)
- Experience: Relevant experience in injectable formulation development, technology transfer, and pharmaceutical product development.
Required Skills
- Injectable Formulation Development
- Parenteral Drug Products
- Technology Transfer
- Process Development & Optimization
- Lyophilization
- Process Validation
- GMP Compliance
- Clinical Trial Supply
- Regulatory Documentation
- OOS, OOT & CAPA Management
- Data Integrity
- Technical Report Writing
This Pharma Research Job at Syngene offers an excellent opportunity for formulation scientists to work on injectable drug development, technology transfer, and GMP manufacturing projects. Candidates looking to grow through a Syngene Career can gain valuable experience in complex injectables, clinical supply programs, and global pharmaceutical development while contributing to innovative healthcare solutions.
