394968BR
Apr 16, 2024
Slovenia
About the Role
We are looking for a Senior Manager in Analytical Operations SI (TRD) in Mengeš. The main focus of Senior Manager would be heading and developing young and motivated team in GMP environment, responsible for the qualification of lab equipment and facilities, seamless sample management, continuous improvements, optimizations, digitalization and automatization of different analytical processes, assuring efficient and fast support to other AO SI teams to achieve common goals, i.e. release of products in clinical phase according to GMP standards.
Your responsibilities:
• Heading the team with responsibility of the development, mentoring, and motivation of the associates.
• Shaping the strategy of the team among other AO SI teams; connecting and tightly collaborating with the global Analytical Development organization.
• Planning and ensuring capacities within the team, to enable and support our AO core business.
• Promoting quality and assuring all GMP activities are performed in a compliant way and on time.
• Drive and encourage optimization, harmonization, actively promote and run digitalization and automation initiatives within the team and across the TRD organization.
• Ensuring compliance of activities with quality standards (GMP), safety standards (HSE) and other Novartis standards
Your responsibilities:
• Heading the team with responsibility of the development, mentoring, and motivation of the associates.
• Shaping the strategy of the team among other AO SI teams; connecting and tightly collaborating with the global Analytical Development organization.
• Planning and ensuring capacities within the team, to enable and support our AO core business.
• Promoting quality and assuring all GMP activities are performed in a compliant way and on time.
• Drive and encourage optimization, harmonization, actively promote and run digitalization and automation initiatives within the team and across the TRD organization.
• Ensuring compliance of activities with quality standards (GMP), safety standards (HSE) and other Novartis standards
Diversity & Inclusion / EEO
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Role Requirements
• Technical expert in pharmaceutical technology, biotechnology, biochemistry, chemical engineering or other relevant discipline with PhD and 2 years relevant experience
or Master of Science with 6 years of relevant experience
• Experience with analytical lab designs and processes, preferable in an industrial setting (biotechnology), knowledge on GMP standard and regulations
• Excellent communication, presentation and management skills
• Proficiency in oral and written English.
Desirable:
• Experience with people management would be an advantage.
• Knowledge of data science and passion for driving digitalization and automatization initiatives would be an advantage and highly desirable.
• Knowledge of project management would be highly desirable.
• Knowledge of GMP standard and regulation would be highly desirable.
We are looking for responsible, objective-driven candidates who value collaboration, teamwork and are open to new challenges and expanding their knowledge and expertise.
We offer permanent contract with 6 months of probation period, work in a dynamic environment, collaboration with different teams, knowledge and experience sharing within the global Novartis system. You are kindly encouraged to submit your application, including CV, by 8.April, 2024.
Accessibility and accommodation: Novartis is 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 recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
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
You’ll receive: 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
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: https://talentnetwork.novartis.com/network
or Master of Science with 6 years of relevant experience
• Experience with analytical lab designs and processes, preferable in an industrial setting (biotechnology), knowledge on GMP standard and regulations
• Excellent communication, presentation and management skills
• Proficiency in oral and written English.
Desirable:
• Experience with people management would be an advantage.
• Knowledge of data science and passion for driving digitalization and automatization initiatives would be an advantage and highly desirable.
• Knowledge of project management would be highly desirable.
• Knowledge of GMP standard and regulation would be highly desirable.
We are looking for responsible, objective-driven candidates who value collaboration, teamwork and are open to new challenges and expanding their knowledge and expertise.
We offer permanent contract with 6 months of probation period, work in a dynamic environment, collaboration with different teams, knowledge and experience sharing within the global Novartis system. You are kindly encouraged to submit your application, including CV, by 8.April, 2024.
Accessibility and accommodation: Novartis is 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 recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
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
You’ll receive: 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
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: https://talentnetwork.novartis.com/network
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
Development
TECHNICAL R & D GDD
Slovenia
Menges
NVS Farmacevtska Proi. doo
Research & Development
Full Time
Regular
No
