395289BR
Mar 26, 2024
USA
About the Role
Location: Millburn New Jersey
At Advanced Accelerator Applications, a Novartis company, we are committed to leading innovation in nuclear medicine and delivering the next generation of targeted radioligand therapy to cancer patients. We are looking for a Site Head of Manufacturing Science and Technology (MSAT) to help us reach our ambitious goals.
As the Site Head, MSAT, you will be responsible for leading the MS&T organization, scientific oversight of manufacturing processes, and ensuring product stewardship, across process units and functions at the Millburn Site.
This role reports directly into the Millburn Site Head and will also be part of the Site Leadership Team.
Key Responsibilities:
• Ensure robust product stewardship for all products manufactured at the site, and end-to-end technical oversight of product manufacturing processes, at all stages of the commercial lifecycle.
•Support excellence in manufacturing through standard setting and technical capability development and deployment. Identify and address process issues.
•Make sure that departments execute and maintain Validation Master Plan activities including the annual revalidation process and cleaning procedures.
•Encourage the identification and implementation of new technologies.
•Work collaboratively with functional management in technical research and development.
•Drive a culture of quality and compliance across the MSAT team.
At Advanced Accelerator Applications, a Novartis company, we are committed to leading innovation in nuclear medicine and delivering the next generation of targeted radioligand therapy to cancer patients. We are looking for a Site Head of Manufacturing Science and Technology (MSAT) to help us reach our ambitious goals.
As the Site Head, MSAT, you will be responsible for leading the MS&T organization, scientific oversight of manufacturing processes, and ensuring product stewardship, across process units and functions at the Millburn Site.
This role reports directly into the Millburn Site Head and will also be part of the Site Leadership Team.
Key Responsibilities:
• Ensure robust product stewardship for all products manufactured at the site, and end-to-end technical oversight of product manufacturing processes, at all stages of the commercial lifecycle.
•Support excellence in manufacturing through standard setting and technical capability development and deployment. Identify and address process issues.
•Make sure that departments execute and maintain Validation Master Plan activities including the annual revalidation process and cleaning procedures.
•Encourage the identification and implementation of new technologies.
•Work collaboratively with functional management in technical research and development.
•Drive a culture of quality and compliance across the MSAT team.
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:
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:
- Novartis: e-mail [email protected] or call +1 (877)395-2339
- Sandoz: e-mail [email protected] or call: +1-609-422-4098
Role Requirements
Essential Requirements:
• Bachelor’s Degree in Science, Pharmacy or Chemical Engineering, Pharmaceutical Technology. Masters or PhD preferred.
• Minimum 6 years’ experience in pharmaceutical manufacturing including demonstrated experience driving quality and compliance in an organization.
• Fundamental understanding of standard pharmaceutical analytical testing.
• Strong working knowledge of applied statistics, quality systems and regulatory requirements across multiple health authorities.
Desirable Requirements:
• Prior experience with aseptic manufacturing and radio pharmaceuticals is a plus.
• Additional experience such as pharmaceutical formulation, process development, or manufacturing technology, is preferred.
Why Novartis? Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture
The pay range for this position at commencement of employment is expected to be between $144,000.00 and $216,000.00 per year; however, while salary ranges are effective from 1/1/24 through 12/31/24 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.
You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards.
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(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: Novartis Talent Pool.
• Bachelor’s Degree in Science, Pharmacy or Chemical Engineering, Pharmaceutical Technology. Masters or PhD preferred.
• Minimum 6 years’ experience in pharmaceutical manufacturing including demonstrated experience driving quality and compliance in an organization.
• Fundamental understanding of standard pharmaceutical analytical testing.
• Strong working knowledge of applied statistics, quality systems and regulatory requirements across multiple health authorities.
Desirable Requirements:
• Prior experience with aseptic manufacturing and radio pharmaceuticals is a plus.
• Additional experience such as pharmaceutical formulation, process development, or manufacturing technology, is preferred.
Why Novartis? Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture
The pay range for this position at commencement of employment is expected to be between $144,000.00 and $216,000.00 per year; however, while salary ranges are effective from 1/1/24 through 12/31/24 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.
You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards.
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(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: Novartis Talent Pool.
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
Operations
Radio Ligand Therapy
USA
Millburn, NJ
AAA USA Inc.
Technical Operations
Full Time
Regular
No
