Abhaysingh Deshmukh

About Abhaysingh Deshmukh

I am a pharmaceutical Project Manager with 8+ years of experience leading GMP-regulated drug development and manufacturing projects across IND, clinical, and commercial stages within global CDMO environments.My background includes CMC execution, technology transfer, and cross-functional project delivery, partnering with formulation, analytical, quality, manufacturing, supply chain, and regulatory teams to ensure schedule reliability, regulatory compliance, and risk-based execution. I have managed complex project portfolios involving clinical trial material and commercial manufacturing, with responsibility for project plans, timelines, budgets, and operational outcomes.I am particularly effective in roles that require- Translating scientific, CMC, and regulatory requirements into clear, executable project plans- Coordinating multi-site, cross-functional teams in GMP manufacturing environments- Proactively identifying and mitigating technical, regulatory, and operational risks- Supporting operational excellence initiatives, including cycle-time and delivery improvements- Communicating clearly with clients, internal stakeholders, and leadership teamsMy work sits at the intersection of science, operations, and execution, with a consistent focus on manufacturing readiness, timely project delivery, and compliance in highly regulated pharmaceutical settings.Core keywords:Project Management | GMP | CMC | Tech Transfer | CDMO | Drug Product | IND | NDA | Clinical Manufacturing | Commercial Manufacturing | Regulatory Compliance | Pharma Operations

Experience

1. Project Manager

   Piramal Pharma Solutions

   Jan 2024 — Present · Sellersville, PA, US

   Cross-Functional Collaboration: Successfully led cross-functional teams, including R&D, QA/QC, manufacturing, and supply chain, to ensure seamless project execution within the CDMO environment.• Project Lifecycle Management: Managed end-to-end project lifecycles, from project initiation and planning to execution, monitoring, and delivery, ensuring alignment with client requirements and timelines.• Client Relationship Management: Acted as the primary point of contact for clients, fostering strong relationships, addressing concerns promptly, and ensuring satisfaction through regular updates and transparent communication.• Regulatory Compliance: Ensured project adherence to regulatory guidelines (FDA, EMA, ICH) and quality standards, supporting audits and providing documentation for successful product approvals.• Process Improvement: Implemented process optimization initiatives to enhance efficiency, reduce project timelines, and improve overall resource utilization within the CDMO framework.

Education

• Lamar University

  Master of Science (M.S.), Chemistry and Biochemistry

  2014 — 2017

• Department Of Pharmaceutical Sciences R.T.M.N.U, Nagpur

  Bachelor of Pharmacy (B.Pharm.), Pharmaceutical Sciences

  2009 — 2013

Skills

• Sds-Page
• Microsoft Word
• Biotechnology
• Protein Purification
• Research
• Protein Expression
• Pharmaceutical Industry
• Dsc
• Spectroscopy
• Molecular Biology
• Cell Biology
• Microsoft Office
• Ftir
• Chemistry
• Powerpoint
• Microsoft Excel
• Pharmaceutics
• Drug Discovery
• Gas Chromatography
• Project Management
• Cross-Functional Team Leadership
• Biochemistry
• Nuclear Magnetic Resonance (Nmr)
• Lead Generation
• Scientific Writing
• Data Analysis
• Fluorescence Spectroscopy
• Differential Scanning Calorimetry
• Cgmp Practices
• Life Sciences
• Hplc
• Community Development
• Teamwork
• Leadership
• Protein Chemistry
• High-Performance Liquid Chromatography (Hplc)
• Pharmacology
• Cell Culture
• Uv/Vis Spectroscopy
• Good Clinical Practice (Gcp)