Site MS&T Head

U469 (FCRS = US469) AAA USA Inc.; Millburn (NJ); On-site; USD 139,000 - 257,000; Full time

Job summary

Novartis in Millburn, NJ seeks a Site MS&T Head to lead Manufacturing Science & Technology, driving validation strategy, technology transfers, process optimization, and compliance across site operations.

You will build and mentor a high-performing MS&T organization, partner with global teams, and serve as the primary technical interface for regulatory authorities while delivering continuous improvement and product stewardship.

Qualifications

• Master of Science degree in Science, Pharmacy, Chemical Engineering, Pharmaceutical Technology, or equivalent experience.
• Minimum 6 years experience within pharmaceutical manufacturing; RLT experience preferred.
• Additional specialist experience in pharmaceutical formulation, process development, manufacturing technology, or related technical disciplines is preferred.
• Proven experience driving quality and compliance within an organization.
• Strong working knowledge of applied statistics, quality systems, and regulatory requirements across multiple health authorities.
• Fundamental understanding of standard pharmaceutical analytical testing.

Responsibilities

• Lead scientific oversight of manufacturing processes to ensure robust, compliant, and reliable product performance.
• Drive product stewardship and technical oversight throughout the commercial lifecycle of site products.
• Own the site Validation Master Plan and ensure execution of validation and revalidation activities.
• Maintain process knowledge, monitor critical process parameters, and sustain validated manufacturing processes.
• Lead technology transfers, technical changes, and commercial scale-up activities in partnership with global teams.
• Serve as the primary technical interface for regulatory authorities and cross-site product-related initiatives.
• Build and develop a high-performing MS&T organization that advances technical excellence, quality, and innovation.

Skills

Applied Statistics

Leadership

Manufacturing Production

Manufacturing Technologies

Operational Excellence

Process Control

Quality Compliance

Regulatory Compliance

Technical Leadership

Technology Transfer

Education

Master of Science

Job description

Band Level 5 Job Description Summary

Location: Millburn, NJ. Relocation Support: This role is based in Millburn, NJ. Novartis is unable to offer relocation support: please only apply if accessible.

Are you ready to shape the future of pharmaceutical manufacturing and scientific innovation? As the Site MS&T Head, you will play a pivotal leadership role in ensuring the technical excellence, robustness, and continuous improvement of manufacturing processes that deliver life-changing medicines to patients. Leading a high-performing Manufacturing Science & Technology (MS&T) team, you will drive product stewardship, validation strategy, technology transfers, process optimization, and compliance excellence while partnering across functions to advance innovation, quality, and operational performance at the site.

Job Description Key Responsibilities

• Lead scientific oversight of manufacturing processes to ensure robust, compliant, and reliable product performance.
• Drive product stewardship and technical oversight throughout the commercial lifecycle of site products.
• Own the site Validation Master Plan and ensure execution of validation and revalidation activities.
• Maintain process knowledge, monitor critical process parameters, and sustain validated manufacturing processes.
• Lead technology transfers, technical changes, and commercial scale-up activities in partnership with global teams.
• Serve as the primary technical interface for regulatory authorities and cross-site product-related initiatives.
• Build and develop a high-performing MS&T organization that advances technical excellence, quality, and innovation.

Essential Requirements

• Master of Science degree in Science, Pharmacy, Chemical Engineering, Pharmaceutical Technology, or equivalent experience.
• Minimum 6 years experience within pharmaceutical manufacturing; RLT experience preferred.
• Additional specialist experience in pharmaceutical formulation, process development, manufacturing technology, or related technical disciplines is preferred.
• Proven experience driving quality and compliance within an organization.
• Strong working knowledge of applied statistics, quality systems, and regulatory requirements across multiple health authorities.
• Fundamental understanding of standard pharmaceutical analytical testing.

The salary for this position is expected to range between $138,600 and $257,400 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.

https://www.novartis.com/careers/careers-research/notice-all-applicants-us-job-openings

Salary Range $138,600.00 - $257,400.00

Skills Desired

• Applied Statistics
• Leadership
• Manufacturing Production
• Manufacturing Technologies
• Operational Excellence
• Process Control
• Quality Compliance
• Regulatory Compliance
• Technical Leadership
• Technology Transfer

EEO Statement: The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.

Accessibility and reasonable accommodations The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an e-mail to [e-mail] call [phone] and let us know the nature of your request and your contact information. Please include the job requisition number in your message. https://www.novartis.com/careers/careers-research/notice-all-applicants-us-job-openings

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