Key Responsibilities:

• Lead the design, development, validation, and implementation of rapid sterility testing methods for cell therapy products.
• Develop and optimize procedures for sterility testing to ensure compliance with regulatory standards and guidelines.
• Collaborate with Regulatory CMC team to prepare and review regulatory submissions and responses related to sterility testing methods.
• Serve as subject matter expert in sterility testing, providing guidance and support to project teams and stakeholders.
• Drive continuous improvement initiatives to enhance sterility testing efficiency and reliability.
• Conduct risk assessments and implement mitigation strategies for sterility testing processes.
• Stay current on industry trends, advancements, and regulatory changes related to sterility testing and cell therapy.
• Establish and maintain relationships with external vendors, service providers, and regulatory agencies.
• Prepare and present technical reports, summaries, protocols, and standard operating procedures (SOPs).

Qualifications:

• Bachelors degree, M.S., or Ph.D in Microbiology, Cell Biology, Biotechnology or a related discipline with a proven track record. Advanced education degree is preferred
•  At least 8 years of experience in industry, academia or relevant experience
• Strong understanding of regulatory requirements for sterility testing in the cell therapy industry (e.g. FDA, EMA, ICH guidelines) is required
• Strong ability with self directed learning to figure things out by reading scientific papers, keeping up with industry trends, and understanding regulatory guidance
• Excellent technical leadership skills, with a team player mentality.
• Demonstrated ability to work independently and as part of a multidisciplinary team.
• Excellent problem-solving skills and the ability to handle multiple projects simultaneously.
• Strong written and verbal communication skills, with the ability to clearly present complex scientific data to various audiences.

Preferred Qualifications:

• Experience in cell and gene therapy product development and manufacturing
• Knowledge of rapid microbial detection systems and advanced microbiology techniques.
• Familiarity with statistical analysis for method validation
• Prior experience working with health authorities or regulatory inspections related to sterility methods
• Industry experience in the development and implementation of rapid microbiology assays for routine batch release
• Proficiency in the development, validation, and implementation of testing methods in a GMP environment is highly desirable

Novartis Compensation and Benefit Summary: The pay range for this position at commencement of employment is expected to be between $145,600-$270,400; however, while salary ranges are effective from 1/1/25 through 12/31/25, fluctuations in the job market may necessitate adjustments to pay ranges during this period.  Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills, and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.