What are the responsibilities and job description for the Sterility Assurance Lead position at Novartis?
Summary
This position will be located at Durham, NC and will not have the ability to be located remotely.
The Sterility Assurance Lead serves as the key functional expert for aseptic processing at the Durham, NC facility. The incumbent will be responsible for providing technical leadership, direction, and management of sterility assurance quality operations to support aseptic manufactured products. This includes the development and optimization of current processes and programs to ensure compliance with regulatory requirements, organizational development, and making appropriate decisions and recommendations to address trends, issues, or significant observations related to sterility assurance.
Key Responsibilities
About the Role
Company will not sponsor visas for this position.
Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.
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
Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards
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, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.
Accessibility & 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 to perform the essential functions of a position, please send an e-mail to [email protected] or 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.
This position will be located at Durham, NC and will not have the ability to be located remotely.
The Sterility Assurance Lead serves as the key functional expert for aseptic processing at the Durham, NC facility. The incumbent will be responsible for providing technical leadership, direction, and management of sterility assurance quality operations to support aseptic manufactured products. This includes the development and optimization of current processes and programs to ensure compliance with regulatory requirements, organizational development, and making appropriate decisions and recommendations to address trends, issues, or significant observations related to sterility assurance.
Key Responsibilities
- Provides leadership and oversight to Quality Operations aseptic oversight.
- Lead supervision of aseptic processing monitoring (Aseptic Process Simulation)
- Review, approve, and provide input to the Contamination Control Strategy for the site
- Provide quality assurance oversight/support of microbiological aspects related to manufacturing as environmental monitoring, gas/water monitoring and Bioburden monitoring.
- Lead and/or contribute to global aseptic projects including stakeholder management.
- Review, approve, and provide input and support of conceptual procedures in aseptic behavior and aseptic processes and ensuring their implementation as well as ensuring compliance with current regulatory requirements
- Supports development and implementation of contamination control strategies
- Provide oversight for product/process deviations, local and global escalations, change controls and audits/inspections, ensuring escalation and remediation of critical issues related to aseptic processes.
- Support root cause investigation and CAPA initiatives for microbiological contamination events/deviations
- Support root cause investigation and CAPA initiatives for microbiological contamination events/deviations
- Provide QA oversight and support microbiological/aseptic best practices training program development and execution to foster culture of compliance and excellence
- Collaborate closely with site operations and quality to integrate comprehensive microbiological control measures site-wide
About the Role
- B.S. degree in scientific field preferably in Microbiology with 6 years’ experience in biopharmaceutical based GMP manufacturing operations including direct experience in managing sterility assurance programs for biotechnology manufacturing facilities or Master’s Degree with 6 years’ experience in biopharmaceutical based GMP manufacturing operations including direct experience in managing sterility assurance programs for biotechnology manufacturing facilities
- Deep understanding of microbiology.
- Understanding of aseptic processes.
- Comprehensive knowledge of FDA and EMA regulations and experience in US and international regulatory agency inspections.
- Excellent verbal, written communication skills and the ability to interface with multiple areas within the organization is essential.
- Ability to synthesize data and summarize outcomes to provide recommendations on a compliant path forward for microbial contamination events.
- Demonstrated ability to perform long-term project planning, team building, budgeting and operational excellence.\
- The global nature of the job requires the position to have excellent knowledge of the various regulatory and GMP requirements as well as outstanding communication skills.
- Strong biotech background in cGMP Manufacturing of Drugs
Company will not sponsor visas for this position.
Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.
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
Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards
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, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.
Accessibility & 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 to perform the essential functions of a position, please send an e-mail to [email protected] or 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.
Salary : $132,300 - $245,700
