Mr. Milind V. jog

CEO,
Proficient,
Pune 411004, India
Mobile : +91- 7588682664 / 9323794677
Email : milindjog.proficient@gmail.com | milind.jog@proficient.net.in

Core Competence :
  • Facility design for pharma / Biotech Formulation and API projects.
  • Finalization of the Basis of Design (BOD), process sizing and process equipment sizing.
  • Basic Engineering including concept development, layouts, process equipment specifications and allied work.
  • Qualification of Process equipment and clean utility systems.
  • Cleaning Validation – VMP preparation, Documentation, Matrix development, associated training
  • GMP-related training – both on-site and off-site
  • GMP compliance Audits of API and Formulation facilities
  • Technical Due diligence
Academic Qualification :
  • M. Pharm. (Pharmacology), Panjab University, Chandigarh, India
Teaching Experience :
  • 1982-1983: College of Pharmacy, Solapur, India (Lecturer in Pharmaceutics and Pharmaceutical Chemistry)
  • 1985-1986: College of Pharmacy, Nashik (Honorary Research Guide for M. Pharm. (Pharmacology)
Industrial Career :
  • 1983-1995: Glaxo India Ltd., Nashik, India (Executive-Production) Responsible for manufacturing management of Tablets, Liquid Orals, Ointments and Sterile Ointments.
  • 1995-2002: Glaxo Saudi Arabia Ltd., Jeddah, Saudi Arabia. (Manager- Production) Responsible for manufacturing management of Tablets, Liquid Orals, Ointments & Creams, General Injectables, Respiratory Solutions, Pressurised Metered Dose Inhalers (PMDI), Cephalosporin Tablets and Powder Injectables.
Consultant to Pharma and Biotech Industry :
  • 2002 – 2007: Mott MacDonald (I) Ltd., Mumbai, India
  • 2007 – 2012 Technolutions Projects Pvt. Ltd. (TPPL), Thane, India
  • 2012-2018: Biopharmax, Pune, India
  • 2006-current:
Joined TPPL as a partner in 2007. Major work responsibilities:
  • Facility design
  • Qualification of Process equipment and clean utility systems.
  • Cleaning Validation
  • GMP-related training – both on-site and off-site
  • GMP compliance Audits of API and Formulation facilities
  • Technical Due diligence
  • Biopharmax, Pune, India (2012-2018)
Joined Biopharmax as V.P. Quality and Facility Design in 2012. Major work responsibilities:
  • Facility design
  • Qualification of Process equipment and clean utility systems.
  • Cleaning Validation
  • GMP-related training – both on-site and off-site
  • GMP compliance Audits of API and Formulation facilities
  • Technical Due diligence
Proficient, Pune, India (2006-2007, 2012-)
Revived operations of Proficient to operate from Pune in 2012.
Major services provided:
  • Facility design – Concept, Basic and Detailed Engineering services
  • Facility Upgradation
  • Qualification of Process equipment and clean utility systems.
  • Assessment of risk of cross-contamination and recommendations (corrective measures)
  • Cleaning Validation
  • GMP-related training – both on-site and off-site  
  • GMP compliance Audits of API and Formulation facilities
  • Technical Due diligence
  • Audits and upgradation of HVAC & other Clean Utilities to improve compliance, efficiency, and performance.