Key Responsibilities

• Lead sterility assurance strategy with primary focus on U.S. manufacturing and FDA regulatory expectations.
• Drive U.S. inspection readiness and remediation programs, partnering with sites to prevent repeat observations.
• Serve as Global Process Owner for Sterile Operations, governing and harmonizing aseptic processes across platforms and sites.
• Provide proactive sterility assurance leadership during the design and qualification of new production facilities and microbiology laboratories, ensuring that layouts, processes, and controls meet all relevant regulatory, aseptic, and quality compliance requirements.
• Serve as subject matter expert in microbiological topics, leading resolution of sterility and contamination escalations.
• Lead complex, cross-functional and cross-site projects delivering U.S. sterility assurance priorities and global quality initiatives.
• Monitor sterility assurance performance indicators and deliver clear, executive-level insights to enable timely, compliant decision-making.
• Represent Novartis externally as a recognized sterility assurance expert, supporting U.S. industry engagement and global alignment.

Essential Requirements

• Bachelor’s degree in pharmacy, chemistry, microbiology, or a related scientific discipline; advanced degree preferred.
• Minimum of 10 years of experience in global, cross-disciplinary project management and leadership roles within the pharmaceutical industry, preferably in strategic Site or global QA Operations and/or Compliance roles. Pharmaceutical production experience is indispensable.
• Extensive experience delivering sterility assurance leadership within U.S. pharmaceutical manufacturing and FDA-regulated environments.
• Deep technical expertise in microbiology, aseptic processing, and sterile manufacturing operations.
• Demonstrated success leading enterprise-level quality initiatives across multiple sites and manufacturing platforms.
• Proven ability to influence senior stakeholders, lead cross-functional teams, and drive complex, high-impact programs.
• Travel up to 25%

The salary for this position is expected to range between $168,000 and $ 312,000 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.

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