PRASHANT ASHOK DEORE
Guadalajara
Summary
Pharmaceutical R&D professional with 11+ years of experience in formulation development, technology transfer, scale-up, lifecycle management and cross-functional leadership across multinational pharmaceutical companies. Proven record of developing oral solid and liquid dosage forms for regulated and international markets.
Overview
4
4
Languages
10
10
years of professional experience
Work History
Formulation Scientist
Laboratorios PiSA S.A. de C.V.
11.2025 - Current
- Lead development of solid and liquid oral formulations for international markets.
- Drive technology transfer, process validation, and commercialization activities.
- Manage cross-functional teams across R&D, QA, Regulatory Affairs, Manufacturing, and Procurement.
- Support regulatory submissions and technical query responses.
Executive – Formulation Development
Ajanta Pharma
12.2024 - 11.2025
- Managed multiple product development programs for regulated and emerging markets.
- Coordinated development activities from laboratory scale through technology transfer.
- Supported successful regulatory and commercialization objectives.
Senior Research Officer - Formulation Development
Glenmark Pharmaceuticals Ltd.
12.2020 - 12.2024
- Developed and optimized oral solid dosage formulations.
- Conducted scale-up, validation, and troubleshooting activities.
- Supported global product registration and lifecycle management.
Executive – Formulation Development
Raptakos Brett & Co.
05.2019 - 12.2020
Officer – Formulation Development
Umedica Laboratories
09.2018 - 04.2019
Research Associate – Formulation Development
IPCA Laboratories
05.2016 - 09.2018
Education
Ph.D. - Pharmacy
Pacific University
Udaipur, India01-2025
Master of Pharmacy - Pharmaceutics
North Maharashtra University
India01-2016
Bachelor of Pharmacy -
Pune University
India01-2014
Skills
- Design Expert
- Microsoft Office
- QbD Tools
- Statistical Analysis
- GMP Documentation
Websites, Portfolios, Profiles
https://www.linkedin.com/in/dr-prashant-deore-phd-7b7aa2b0?utm_source=share_via&utm_content=profile&utm_medium=member_android
LANGUAGES
English (Professional)
Spanish (Intermediate)
Hindi (Native)
Marathi (Native)
REFERENCES
Available upon request.
KEY CAREER ACHIEVEMENTS
- Developed 20+ oral solid and liquid pharmaceutical products for regulated and emerging markets.
- Led technology transfer activities across multiple manufacturing sites.
- Successfully managed cross-functional teams involving R&D, Regulatory Affairs, QA, Manufacturing and Procurement.
- Supported product registrations for international markets.
- Reduced development timelines through risk-based formulation strategies.
CORE LEADERSHIP COMPETENCIES
- Formulation Development
- Oral Solid Dosage Forms
- Liquid Dosage Forms
- Technology Transfer
- Process Validation
- Scale-Up
- Quality by design (QbD)
- Risk Assessment
- CGMP
- Regulatory Support
- Lifecycle Management
- Project Management.
AREA OF EXPERTISE
- Championed scientific innovation to overcome formulation, manufacturing and technical challenges.
- Established proactive risk management frameworks to drive project success and regulatory compliance.
- Governed technical documentation, quality systems and cGMP compliance across development programs.
- IR/ER Tablets, ODTs, Capsules, Pellets, Syrups, Suspensions, Wet Granulation, Fluid Bed Processing, Roller Compaction.
INTERNATIONAL MARKET EXPOSURE
- USFDA
- EMA
- MHRA
- WHO
- TGA
- Health Canada
ADDITIONAL INFORMATION
- Temporary Resident of Mexico
- Valid US B1/B2 Visa
- Available for international travel
- Open to relocation within the UK, Europe, Middle East, Asia-Pacific and North America
- Eligible to work under employer-sponsored visa programs.
PUBLICATIONS
- Research article | Formulation and development of Solifenacin succinate oral suspension, IJDDT,15(2),2025.
- Review article | Quality by design (Qbd) is novel approach for risk assessment of Oral liquid formulations, WJPMR,11(6),2025.
- Review article | A review: quality by design (Qbd) is novel approach for development of pharmaceutical, WJPR,5(9),2016.
- Research article | Formulation and evaluation of nicotine buccal film, IJRPN5,5(2),2016.
Timeline
Formulation Scientist
Laboratorios PiSA S.A. de C.V.
11.2025 - Current
Executive – Formulation Development
Ajanta Pharma
12.2024 - 11.2025
Senior Research Officer - Formulation Development
Glenmark Pharmaceuticals Ltd.
12.2020 - 12.2024
Executive – Formulation Development
Raptakos Brett & Co.
05.2019 - 12.2020
Officer – Formulation Development
Umedica Laboratories
09.2018 - 04.2019
Research Associate – Formulation Development
IPCA Laboratories
05.2016 - 09.2018
Ph.D. - Pharmacy
Pacific University
Master of Pharmacy - Pharmaceutics
North Maharashtra University
Bachelor of Pharmacy -
Pune University