The Role:
This is a newly created role in the New Manufacturing and Expansions department to support Moderna’s new site startup and continue manufacturing activities. Based in Lava, Canada; this role will lead a group of 2 to 5 scientists and engineers responsible for technology transfer, process start-up, drug substance manufacturing process validations, and commercial cGMP manufacturing support.
The Site Drug Substance MST Lead will lead a team responsible for technical support of Moderna cGMP manufacturing activities at the new facility in Laval, Canada. Working alongside Moderna’s manufacturing operations and QA teams, the MST Lead will lead collaborative teams that establish and sustain Moderna’s cGMP manufacturing processes.
Here’s What You’ll Do:
Ensure successful technology transfer of Moderna processes into manufacturing operations. Manage and document process and project information with a robust documentation package.
Be the point of contact for manufacturing issues requiring technical investigations. Identify root cause. Coordinate and resolve issues with effective CAPAs
Ensure successful validation of Moderna manufacturing processes at the respective site.
Manage change as part of a Global Change Control forum
Maintain alignment with other global manufacturing sites through shared knowledge, shared manufacturing data, shared manufacturing issues, and common solutions.
Lead a diverse group of scientists and engineers by establishing common practices, establishing a data-driven culture, using metrics for improvements, and being hands on in risk assessment and defining solutions.
Actively participate in health authorities' audits
Here’s What You’ll Bring to the Table:
M.S. or Ph.D. in a technical discipline related to Pharmaceutical Manufacturing (Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Engineering, etc.)
A minimum of 10 years of related work experience
Prior managerial experience. Ability to mentor staff in technical areas outside your area of expertise
Direct experience providing technical support of cGMP manufacturing operations in biologics manufacturing or parenteral drug product manufacturing. Experience includes technology transfer, investigations, and change management.
Experience using statistical process control and process analytics for monitoring and improving control of processes.
Demonstrated capability of working cross-functionally in a technical area outside of core expertise.
Experience supporting commercial cGMP manufacturing processes preferred.
Le rôle :
Ce poste a été créé au sein du département de la fabrication et des expansions pour soutenir le démarrage du nouveau site de Moderna et poursuivre les activités de fabrication. Basé à Laval, Canada, ce rôle dirigera un groupe de 2 à 5 scientifiques et ingénieurs responsables du transfert de technologie, du démarrage des processus, de la validation des processus de fabrication de substances médicamenteuses et du soutien à la fabrication commerciale conforme aux BPF.
Le responsable MST (Manufacturing Science and Technology) pour la substance médicamenteuse dirigera une équipe chargée du soutien technique des activités de fabrication conformément aux BPF de Moderna sur le nouveau site de Laval, Canada.
Voici ce que vous ferez :
Assurer le transfert des processus de Moderna vers les opérations de fabrication. Gérer et documenter les informations sur les processus et les projets avec un ensemble de documentation solide.
Être le point de contact pour les problèmes de fabrication nécessitant des enquêtes techniques. Identifier la cause. Coordonner et résoudre les problèmes avec des CAPA efficaces.
Assurer la validation des processus de fabrication de Moderna sur le site en question.
Gérer les changements dans le cadre d'un forum mondial de contrôle des changements.
Maintenir l'alignement avec les autres sites de fabrication mondiaux grâce au partage de connaissances, de données de fabrication, et de solutions communes.
Diriger un groupe diversifié de scientifiques et d'ingénieurs en établissant des pratiques communes, en instaurant une culture axée sur les données, en utilisant des indicateurs d’amélioration et en étant impliqué dans l'évaluation des risques et la définition des solutions.
Participer activement aux audits des autorités sanitaires.
Voici ce que vous apporterez (Qualifications requises) :
M.S. ou Ph.D. dans une discipline technique liée à la fabrication pharmaceutique (chimie, biochimie, génie chimique, génie pharmaceutique, etc.).
Un minimum de 10 ans d'expérience professionnelle en lien avec le domaine
Expérience antérieure en gestion d’équipe. Capacité à encadrer le personnel dans des domaines techniques en dehors de votre domaine d'expertise.
Expérience directe dans le soutien technique des opérations de fabrication conforme aux BPF dans la fabrication de produits biologiques ou de produits pharmaceutiques parentéraux. Une expérience comprenant le transfert de technologie, les enquêtes et la gestion des changements.
Expérience de l'utilisation du contrôle statistique des processus et de l'analyse des processus pour surveiller et améliorer le contrôle des processus.
Capacité démontrée à travailler de manière transversale dans un domaine technique en dehors de son expertise principale.
Expérience dans le soutien des processus de fabrication commerciale conforme aux BPF.
Moderna offers personalized benefit programs and well-being resources as unique as our global workforce so employees can do their best work.
We recognize and appreciate your diverse needs and interests and do our best to support you at work and at home with:
Quality healthcare and insurance benefits
Lifestyle Spending Accounts to create your own pathway to well-being
Free premium access to fitness, nutrition, and mindfulness classes
Family planning and adoption benefits
Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, and a discretionary year-end shutdown
Educational resources
Savings and investments
Location-specific perks and extras!
The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.
About Moderna
Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.
By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.
If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.
Moderna is a smoke-free, alcohol-free and drug-free work environment.
Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!
Moderna is proud to be an equal opportunity workplace and is an affirmative action employer.
Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. We’re focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Talent Acquisition Partner or contact the Accommodations team at . (EEO/AAP Employer)
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This is a newly created role in the New Manufacturing and Expansions department to support Moderna’s new site startup and continue manufacturing activities. Based in Lava, Canada; this role will lead a group of 2 to 5 scientists and engineers responsible for technology transfer, process start-up, drug substance manufacturing process validations, and commercial cGMP manufacturing support.
The Site Drug Substance MST Lead will lead a team responsible for technical support of Moderna cGMP manufacturing activities at the new facility in Laval, Canada. Working alongside Moderna’s manufacturing operations and QA teams, the MST Lead will lead collaborative teams that establish and sustain Moderna’s cGMP manufacturing processes.
Here’s What You’ll Do:
Ensure successful technology transfer of Moderna processes into manufacturing operations. Manage and document process and project information with a robust documentation package.
Be the point of contact for manufacturing issues requiring technical investigations. Identify root cause. Coordinate and resolve issues with effective CAPAs
Ensure successful validation of Moderna manufacturing processes at the respective site.
Manage change as part of a Global Change Control forum
Maintain alignment with other global manufacturing sites through shared knowledge, shared manufacturing data, shared manufacturing issues, and common solutions.
Lead a diverse group of scientists and engineers by establishing common practices, establishing a data-driven culture, using metrics for improvements, and being hands on in risk assessment and defining solutions.
Actively participate in health authorities' audits
Here’s What You’ll Bring to the Table:
M.S. or Ph.D. in a technical discipline related to Pharmaceutical Manufacturing (Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Engineering, etc.)
A minimum of 10 years of related work experience
Prior managerial experience. Ability to mentor staff in technical areas outside your area of expertise
Direct experience providing technical support of cGMP manufacturing operations in biologics manufacturing or parenteral drug product manufacturing. Experience includes technology transfer, investigations, and change management.
Experience using statistical process control and process analytics for monitoring and improving control of processes.
Demonstrated capability of working cross-functionally in a technical area outside of core expertise.
Experience supporting commercial cGMP manufacturing processes preferred.
Le rôle :
Ce poste a été créé au sein du département de la fabrication et des expansions pour soutenir le démarrage du nouveau site de Moderna et poursuivre les activités de fabrication. Basé à Laval, Canada, ce rôle dirigera un groupe de 2 à 5 scientifiques et ingénieurs responsables du transfert de technologie, du démarrage des processus, de la validation des processus de fabrication de substances médicamenteuses et du soutien à la fabrication commerciale conforme aux BPF.
Le responsable MST (Manufacturing Science and Technology) pour la substance médicamenteuse dirigera une équipe chargée du soutien technique des activités de fabrication conformément aux BPF de Moderna sur le nouveau site de Laval, Canada.
Voici ce que vous ferez :
Assurer le transfert des processus de Moderna vers les opérations de fabrication. Gérer et documenter les informations sur les processus et les projets avec un ensemble de documentation solide.
Être le point de contact pour les problèmes de fabrication nécessitant des enquêtes techniques. Identifier la cause. Coordonner et résoudre les problèmes avec des CAPA efficaces.
Assurer la validation des processus de fabrication de Moderna sur le site en question.
Gérer les changements dans le cadre d'un forum mondial de contrôle des changements.
Maintenir l'alignement avec les autres sites de fabrication mondiaux grâce au partage de connaissances, de données de fabrication, et de solutions communes.
Diriger un groupe diversifié de scientifiques et d'ingénieurs en établissant des pratiques communes, en instaurant une culture axée sur les données, en utilisant des indicateurs d’amélioration et en étant impliqué dans l'évaluation des risques et la définition des solutions.
Participer activement aux audits des autorités sanitaires.
Voici ce que vous apporterez (Qualifications requises) :
M.S. ou Ph.D. dans une discipline technique liée à la fabrication pharmaceutique (chimie, biochimie, génie chimique, génie pharmaceutique, etc.).
Un minimum de 10 ans d'expérience professionnelle en lien avec le domaine
Expérience antérieure en gestion d’équipe. Capacité à encadrer le personnel dans des domaines techniques en dehors de votre domaine d'expertise.
Expérience directe dans le soutien technique des opérations de fabrication conforme aux BPF dans la fabrication de produits biologiques ou de produits pharmaceutiques parentéraux. Une expérience comprenant le transfert de technologie, les enquêtes et la gestion des changements.
Expérience de l'utilisation du contrôle statistique des processus et de l'analyse des processus pour surveiller et améliorer le contrôle des processus.
Capacité démontrée à travailler de manière transversale dans un domaine technique en dehors de son expertise principale.
Expérience dans le soutien des processus de fabrication commerciale conforme aux BPF.
Moderna offers personalized benefit programs and well-being resources as unique as our global workforce so employees can do their best work.
We recognize and appreciate your diverse needs and interests and do our best to support you at work and at home with:
Quality healthcare and insurance benefits
Lifestyle Spending Accounts to create your own pathway to well-being
Free premium access to fitness, nutrition, and mindfulness classes
Family planning and adoption benefits
Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, and a discretionary year-end shutdown
Educational resources
Savings and investments
Location-specific perks and extras!
The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.
About Moderna
Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.
By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.
If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.
Moderna is a smoke-free, alcohol-free and drug-free work environment.
Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!
Moderna is proud to be an equal opportunity workplace and is an affirmative action employer.
Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. We’re focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Talent Acquisition Partner or contact the Accommodations team at . (EEO/AAP Employer)
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