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Assoc. Director Science & Technology - Cell Therapy Process Analytics

Management

Executive Director

No

East Hanover, New Jersey, United States

Assoc. Director Science & Technology - Cell Therapy Process Analytics

Job ID

392180BR

Feb 14, 2024

USA

About the Role

Join Our Vision: At Novartis, we are on the transformative journey in cell therapy, pushing the boundaries of medical innovation. We are currently seeking a dynamic and visionary Associate Director to spearhead our Cell Therapy Process Analytics group. This pivotal role is not just about leading a team; it’s about shaping the future of cell therapy.

Your Role: As the Associate Director, you’ll be at the forefront of our mission, guiding a talented group of scientists dedicated to analytical testing that propels process development. Characterization, and product innovation. Reporting to the Head of Cell Therapy Analytical Development and Operations, you will be a vital link between Analytical Development, Process Development Pilot Plant, and the broader Novartis Operations team.

Your responsibilities include, but are not limited to:

• Manage a team in performing and coordinating non-GMP sample testing across multiple assays. Mentor and train team members, fostering an environment of continuous learning and development.

• Develop and implement analytical strategies for cell therapy process and product characterization.

• Manage complex projects timelines with a strategic approach. Able to balance technical feasibility, opportunity, and impact.

• Fostering collaborative relationships across cross-functional project teams.

• Provide analytical technical expertise in process development and optimization.

• Offer extensive knowledge in analytical tools for cell therapy products, serving as subject matter expert in certain assays such as molecular assays, flow cytometry, and/or potency assays.

• Evaluate and integrate new technologies for product characterization and quality assessment.

• Support manufacturing process investigations and improvements.

Diversity & Inclusion / EEO

We are Equal Opportunity Employers and take pride in maintaining a diverse environment. 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 are committed to building diverse teams, representative of the patients and communities we serve, and 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: Individuals in need of a reasonable accommodation due to a medical condition or disability for any part of the application process, or to perform the essential functions of a position, please let us know the nature of your request, your contact information and the job requisition number in your message:

Role Requirements

What you'll bring to the role:

• Manage a team in performing and coordinating non-GMP sample testing across multiple assays. Mentor and train team members, fostering an environment of continuous learning and development.

• Develop and implement analytical strategies for cell therapy process and product characterization.

• Manage complex projects timelines with a strategic approach. Able to balance technical feasibility, opportunity, and impact.

• Fostering collaborative relationships across cross-functional project teams.

• Provide analytical technical expertise in process development and optimization.

• Offer extensive knowledge in analytical tools for cell therapy products, serving as subject matter expert in certain assays such as molecular assays, flow cytometry, and/or potency assays.

• Evaluate and integrate new technologies for product characterization and quality assessment.

• Support manufacturing process investigations and improvements.

The pay range for this position at commencement of employment is expected to be between $166,400 and $249,600 year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. 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.

Why Novartis?

799 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives?

We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges.

Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

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 [email protected] call +1 [Register to View] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

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

Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network

Division

Development

Business Unit

TECHNICAL R & D GDD

Location

USA

Site

East Hanover, NJ

Company / Legal Entity

Novartis Pharmaceuticals

Functional Area

Research & Development

Job Type

Full Time

Employment Type

Regular

Shift Work

No