Work within expanding and dynamic pharmaceutical client environments
Analyze and resolve complex technical and quality-related issues, including leading or supporting investigations and CAPA activities
Provide expert consulting in microbiology, manufacturing processes, and pharmaceutical quality systems
Collaborate closely with client Quality Assurance (QA) and Operations teams
Support and lead global projects, managing multiple stakeholders across functions and locations
Conduct data-driven analysis and translate findings into clear, actionable recommendations
Communicate effectively with clients at all levels, including the ability to challenge and push back when required to uphold quality and compliance standards
Participate in an approximately three-month onboarding and training program
Requirements
Minimum 10 years of experience in pharmaceutical manufacturing in the Aseptics area
Degree in Microbiology (required)
Master’s degree is a strong asset
Proven project management skills
Deep understanding of pharmaceutical industry processes and regulatory expectations
Excellent verbal and written communication skills, with a high level of effectiveness and confidence in client-facing situations
Ability to work independently in complex, fast-paced, and international environments
Willingness and ability to travel approximately 50% of time internationally