Victor Voronyuk

Director Of Validation, Tech.Ops

Executive Summary & Candidate Overview

Victor brings strong leadership skills to his roles, having managed validation programs and mentored teams to success. His experience spans from establishing validation programs to overseeing multi-discipline validation projects. Victor is adept at ensuring compliance with local, state, and federal regulations, including cGMP standards. He is committed to continuous improvement and process effectiveness.

Accomplishments and Key Performance Indicators (KPIs)

Throughout his career, Victor has successfully led validation programs and managed complex projects, including FDA audit inspections with no validation observations. He has contributed to the successful validation of various processes and products, ensuring their compliance with regulatory requirements. Victor's expertise includes establishing validation master plans, executing validation protocols, and managing risk assessments.

Location and Travel

Open to: On-Site, Hybrid, and Remote Roles
Remote Roles: Willing to consider remote opportunities based on specific position requirements
Compensation Seeking: Open to discussing compensation details upon scheduling a meeting
Position Seeking: Seeking Director-level roles in Validation or Technical Operations within the pharmaceutical industry

Work Experience

Director Of Validation, Tech.Ops
- SCA PHARMACEUTICALS, 2021 to Present
  - Managed validation programs for two manufacturing sites, overseeing global validation life cycle projects and CAPEX projects.
Validation Manager, MS&T
- XELLIA PHARMACEUTICAL, 2019 to 2021
  - Led site validation program, coordinated multi-discipline validation projects, and ensured compliance with regulatory standards.
Manager, Validation Engineering
- AVARA PHARMA TECHNOLOGIES, 2015 to 2019
  - Managed validation projects, reviewed and approved validation documentation, and supported new product introductions.
Validation Manager
- Novartis, 2013 to 2015
  - Implemented site validation program, developed validation master plans, and ensured compliance with cGMP requirements.
Site Validation Manager
- BIONICHE LIFE SCIENCES, 2010 to 2013
  - Responsible for commissioning, qualification, and validation initiatives for a new vaccine manufacturing center, ensuring compliance with regulatory policies.