Pharmaceutical Bioprocess Validation and Compliance Consultant

Technical Consultant #2008


  • Bioprocess engineering specific to equipment (equipment reliability and maintenance), systems and facilities.
  • Bioprocess validation (aseptic processes, equipment, systems, facilities and cleaning).
  • Technological process scale-up from bench top to pilot and commercial manufacturing.
  • Biological active compounds and nanoparticle based drug delivery systems.
  • cGMP manufacturing of pharmaceutical and biopharmaceutical products.
  • Technology transfer to a Contract Manufacturing Organization (CMO) in Canada and U.S.A.
  • Documentation review, disposition and release for cGMP manufacturing (batch records, SOPs, VP and WI).
  • Single-use technologies development and implementation into biopharmaceutical manufacturing.


Undisclosed Company, Senior Consulting Engineer, Present

  • Engineering support in the process validation; equipment and support systems qualification.
  • Consulting services in the disposable technology application for manufacturing of HPAPI (High Potency Active Pharmaceutical Ingredient).
  • Engineering support in contract manufacturing of complex liposome based drug delivery systems.
  • Project lead for the new pilot scale manufacturing facility engineering, validation and start-up.
  • Isolator technology development and application in cGMP manufacturing of drug products.

KDA Triglav Systems Ltd., Vancouver, Canada, BC, Senior Management Consultant, 2009 - 2012

  • Engineering support in the process scale-up and technology transfer to CMOs.
  • Project lead in collaboration with Tacmina Corporation to adapt Smoothflow technology for various biotechnological applications and pharmaceutical manufacturing.
  • Support for regulatory submission through detailed process validation strategy engineering.
  • Consulting services in the single use technology application in biotechnological processes.
  • Consulting services to start-up companies to their support cGMP manufacturing of API and biologics.
  • Engineering support in the process scale-up and technology transfer to CMOs.

Tekmira Pharmaceuticals Corporation, City of Burnaby, Canada, 1997 - 2008


  • Group Leader, Technology Transfer, 2005 - 2008
  • Senior Product Development Engineer, CMC, Manufacturing, 2002 - 2004
  • Scientist III, Research and Development and Product Development, 1997 - 2001


  • Lead role in the development, engineering and the implementation of the scale-up strategy into company's manufacturing technology.
  • Played a key role in the development and implementation of the process and the equipment validation strategy. ~Performed review and approval of QI/OQ/PQ protocols, WI and SOPs, VP and VR.
  • Provided lead support in validation master plan engineering and post approval re-validation program development.
  • Successfully validated cleaning procedures for liposome based formulations and siRNA manufacturing processes.
  • Planned and executed manufacturing operation on site and at CMO for anticancer and immunostimulatory liposomal injectable drug products.
  • Provided daily support and trouble-shooting with all cGMP related manufacturing activities (facilities preparation, equipment maintenance, line clearance).
  • Acted as engineering lead (project manager) in the single use technology application to the aseptic manufacturing of liposome based products on the pilot plant scale.
  • Planning and coordinating the quality assurance activities of vendors, stakeholders and contract resources.
  • Assisted QA department with resolution of quality issues as person in plant representing PD/manufacturing department at a contract manufacturer sites.
  • As a key representative of the manufacturing department, participated in batch record issuance, compilation, review and disposition.
  • Actively participated in development of the manufacturing systems such as non-conformances, FMEA and CAPA, implementation of change control and QbD programs.
  • Led Statistical Process Control, (SPC) analysis in the determination of preventive actions required on the side of CAPA development.
  • Performed batch record review and resolution of deviations with various CMO.
  • Participated in the development of training records for manufacturing personnel of various CMO during technology transfer activities.
  • Performed GLP & GMP audits of laboratories and commercial manufacturing units.
  • Hosting FDA regulatory inspections in cGMP manufacturing facilities and PD laboratories.
  • Participated in cGMP facilities inspection prior to manufacturing campaign and ensuring environmental control.

Honors & Publications


  • Professional Engineer-P.Eng., BC, Canada
  • IT proficient (Wrike, Word, Excel, PowerPoint, Outlook, Databases, Calibration Manager).


  • Russian, mother tongue.
  • Czech, conversational, and reading.


  • WO patent: Production improvement of lipid vesicles.


  • M.S. Process Engineering, State University, Chemical Technology, Moscow, Russian Federation
  • B.S. Process Engineering, State University, Chemical Technology, Moscow, Russian, Federation
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