Santhoshkumar Sivakumar

About Santhoshkumar Sivakumar

As a Formulation Scientist with a passion for transforming scientific concepts into innovative, stable, and effective products of (Oral Solids, Liquid Orals, Injectables & Opthalmics).With hands-on experience in developing and optimizing formulations across the pharmaceuticals. I specialized in bridging the gap between research and real-world application.My core competencies include: Designing and developing new formulations from lab-scale to commercial production. Conducting pre-formulation studies, stability testing, and analytical method development. Implementing QbD (Quality by Design) and DoE (Design of Experiments) for robust, reproducible results. Expertise in product development, scale-up, process optimization, technology transfer and new product introduction. Consistently led teams to achieve successful product launches and outcomes throughout my career. Collaborating cross-functionally with regulatory, quality, and manufacturing teams. Staying informed on regulatory requirements, industry trends, and emerging technologies. Driven by curiosity and a commitment to quality, I take pride in solving complex formulation challenges and contributing to the development of safe, effective, and competitive products. Currently spearheading the development of new technologies and improving product performance in Oral Solid products. Passionate about innovation and scientific discovery, dedicated to pushing the boundaries of technology and solving complex problems. Let me know if you\'d like this tailored with specific technologies, product types, or personal achievements. Open to collaboration, innovation opportunities, and scientific exchange within the formulation and R&D community.

Experience

1. Junior Research Associate in Formulation Development

   Linux Lifesciences

   Mar 2025 — Present · Puducherry, IN

   Oral SolidsDevelop and execute the experiments using Quality by Design approach led to scale up development of formulations. Carry out literature and patent related to formulation and developmental studies. Preparation and Utilization of MFRs, MPRs, Gap Assessment, Process Optimization Protocols cum Reports and Standard Operating Procedure.To review the Product Note Book, Laboratory Scale up Protocol & Report for next level of Lab trails.To work on optimizing the Compounding Process in Oral Solids this can ensure consistency, efficiency and Scalability. To develop from Laboratory or Pilot Scale to full manufacturing, this tends to ensuring that the product maintains its quality and efficacy at larger volumes. To ensuring by conducting Validation studies through Prepared Protocols. Coordinate with Cross Functional departments to fulfill the project objectives. To create a detailed documentation such as Technology Transfer protocols and reports, to track and verify the successful transfer and execution.

Education

• GEETANJALI UNIVERSITY

  Certificate Course in Basics of Gastroenterology and Hepatology (CCBGH), Pharmacology and Toxicology

• GEETANJALI UNIVERSITY

  Master Certificate Course, Diabetic Pharmacotherapy

• Padmavathi College of Pharmacy and Research Institute, Dharmapuri

  Bachelor of Pharmacy, Pharmacy