About the Role
Key Responsibilities
- Serve as site sterility assurance expert for aseptic processing and microbial control programs
- Design, maintain, and improve sterility assurance strategies aligned with global regulatory expectations
- Lead sterility‑related deviations, contamination investigations, and risk‑based decision making
- Own environmental and personnel monitoring strategies, including trending, escalation, and continuous improvement
- Author, review, and approve sterility assurance documentation, validations, and technical rationales
- Represent sterility assurance during regulatory inspections, audits, and quality governance forums
- Partner cross‑functionally to resolve sterility risks and strengthen inspection readiness and compliance
Essential Requirements
- Bachelor’s degree in a scientific or technical field, preferably Microbiology or a related discipline
- Extensive experience supporting sterility assurance programs in regulated biopharmaceutical manufacturing environments
- Deep understanding of aseptic processing, microbial control strategies, and contamination risk management
- Proven experience leading sterility‑related investigations, environmental monitoring programs, and corrective action planning
- Strong knowledge of global regulatory expectations, including United States and European health authority requirements
- Ability to apply scientific judgment, analyze complex data, and communicate clear, compliant recommendations
Desirable Requirements
- Experience supporting sterility assurance activities for aseptic cell or gene therapy manufacturing
- Direct participation in regulatory inspections with ownership of sterility assurance topics and responses
The pay range for this position at commencement of employment is expected to be between $108,500 and $201,500 per year; however, while salary ranges are effective for a defined period, fluctuations in the job market may necessitate adjustments. Final pay determinations will depend on a variety of factors, including but not limited to geographic location, experience level, knowledge, skills, and abilities. The total compensation package may also include other elements, such as a performance‑based bonus and a full range of medical, financial, and other benefits, including retirement programs and paid time off. Details of participation in these benefit plans will be provided if an offer of employment is made. Employment with Novartis is at‑will, and the company reserves the right to modify compensation at any time based on individual, business, or market factors.
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Role Requirements
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.
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