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Senior Manager Regulatory Affairs Lead(m/w/x)
Global regulatory leadership for biosimilar development, managing submission dossiers and health authority meeting preparations. 6-8 years international regulatory experience with global submission (US BLA/EU MAA) required. Global project scope, international team collaboration.
Anforderungen
- Degree in life science or related disciplines
- At least 6-8 years in international regulatory
- Experience in managing international or regional regulatory submissions, normally a full global submission (new product application), preferably US BLA or EU MAA
- Experience in working in development project teams
- Experience in leading regulatory agency interactions including management of the associated documentation and rehearsals
- Experience in preparation and coordination of regulatory strategy plan
- Experience in biological development
- Experience in CTA requirements
- Capability to manage a number and range of projects throughout development
- Excellent written and spoken communication skills
- Excellent interpersonal skills
- Understanding of Regulatory Affairs contribution to Pharma business
- Excellent organizational skills, work independently, self-motivated and proactive
- Attention to details, without losing the overall picture
- Ability to think strategically
- Ability to lead regulatory sub team and work in teams
- Autonomous, goal-oriented and pragmatic
- Strong customer-orientation and strong communication skills
- Fluent command of spoken and written English, additional language skills welcome
Aufgaben
- Provide global regulatory leadership for biosimilar development
- Manage submission-related documents and regulatory data for biosimilars
- Lead preparation and rehearsal for meetings with Health Authorities
- Develop and manage the submission strategy for biosimilar dossiers
- Ensure compliance with Fresenius Kabi regulatory procedures
- Establish regulatory storylines for interactions with authorities
- Collaborate with Regulatory Operations to implement technology strategies
- Support market units in interactions with local health authorities
- Contribute to wave 2 submission prioritization assessments
- Guide Launch Readiness Plans with regulatory process insights
- Lead the Regulatory Sub-team and Strategic Submission Teams as needed
- Act as Regional Lead for US, Canada, or EU regulatory responsibilities
- Manage the regulatory submission process through to approval
- Coordinate regulatory agency interactions and document preparation
- Provide recommendations on submission readiness
- Stay updated on the current regulatory environment
- Interface with other regulatory groups and company functions
- Perform additional tasks to support regulatory objectives
- Drive collaboration with third-party partners for regulatory tasks
- Mentor Junior Regulatory Affairs Leaders
Berufserfahrung
- 6 - 8 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Noch nicht perfekt?
- Fresenius KabiVollzeitnur vor OrtManagementEysins
- Fresenius Kabi SwissBioSim GmbH
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Senior Manager Regulatory Affairs Lead(m/w/x)
Global regulatory leadership for biosimilar development, managing submission dossiers and health authority meeting preparations. 6-8 years international regulatory experience with global submission (US BLA/EU MAA) required. Global project scope, international team collaboration.
Anforderungen
- Degree in life science or related disciplines
- At least 6-8 years in international regulatory
- Experience in managing international or regional regulatory submissions, normally a full global submission (new product application), preferably US BLA or EU MAA
- Experience in working in development project teams
- Experience in leading regulatory agency interactions including management of the associated documentation and rehearsals
- Experience in preparation and coordination of regulatory strategy plan
- Experience in biological development
- Experience in CTA requirements
- Capability to manage a number and range of projects throughout development
- Excellent written and spoken communication skills
- Excellent interpersonal skills
- Understanding of Regulatory Affairs contribution to Pharma business
- Excellent organizational skills, work independently, self-motivated and proactive
- Attention to details, without losing the overall picture
- Ability to think strategically
- Ability to lead regulatory sub team and work in teams
- Autonomous, goal-oriented and pragmatic
- Strong customer-orientation and strong communication skills
- Fluent command of spoken and written English, additional language skills welcome
Aufgaben
- Provide global regulatory leadership for biosimilar development
- Manage submission-related documents and regulatory data for biosimilars
- Lead preparation and rehearsal for meetings with Health Authorities
- Develop and manage the submission strategy for biosimilar dossiers
- Ensure compliance with Fresenius Kabi regulatory procedures
- Establish regulatory storylines for interactions with authorities
- Collaborate with Regulatory Operations to implement technology strategies
- Support market units in interactions with local health authorities
- Contribute to wave 2 submission prioritization assessments
- Guide Launch Readiness Plans with regulatory process insights
- Lead the Regulatory Sub-team and Strategic Submission Teams as needed
- Act as Regional Lead for US, Canada, or EU regulatory responsibilities
- Manage the regulatory submission process through to approval
- Coordinate regulatory agency interactions and document preparation
- Provide recommendations on submission readiness
- Stay updated on the current regulatory environment
- Interface with other regulatory groups and company functions
- Perform additional tasks to support regulatory objectives
- Drive collaboration with third-party partners for regulatory tasks
- Mentor Junior Regulatory Affairs Leaders
Berufserfahrung
- 6 - 8 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Über das Unternehmen
Fresenius Kabi SwissBioSim GmbH
Branche
Pharmaceuticals
Noch nicht perfekt?
- Fresenius Kabi
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