Hovione Benefits Overview

Serves as the global technical authority for microbiology and contamination control across pharmaceutical and biotechnology operations. Leads global policies, GMP standards, contamination control strategies, sterility assurance, environmental monitoring, cleanroom practices, investigations, risk assessments, audits, and regulatory inspection support. Provides technical guidance to cross-functional teams, drives harmonization across sites, delivers training, and leads global quality and continuous-improvement initiatives.

Serves as the enterprise subject matter expert for process validation, cleaning validation, contamination control, new product introduction, and regulatory segregation. Leads quality and regulatory initiatives, complex projects, risk-based decision-making, continuous improvement, and cross-site alignment. Provides technical support on GMP and regulatory requirements across the product lifecycle while maintaining quality systems, documentation, tools, and training.

Performs quality control laboratory testing of pharmaceutical raw materials, intermediates, and finished products in a GMP-regulated environment. Maintains laboratory records, calibrates and maintains instruments, investigates out-of-specification results and deviations, supports audits, and ensures compliance with GMP, HSE, regulatory, and company standards. Coordinates testing schedules, communicates with internal departments, and supports daily laboratory operations.