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Associate Director, Regulatory Affairs CMC(m/w/x)
Leading global CMC submission planning and authoring for diverse pharmaceutical projects. Minimum 8 years regulatory or pharmaceutical experience required. On-site childcare facilities.
Requirements
- Science degree or equivalent
- Minimum 8 years regulatory or pharmaceutical experience
- Knowledge in regulatory submission and CMC issues
- Ability to critically evaluate scientific data
Tasks
- Drive global CMC regulatory strategies for diverse projects
- Lead all global CMC submission planning and authoring
- Coordinate and review technical submission documentation
- Identify and resolve content or quality issues
- Negotiate delivery of technical source documents
- Author high-quality CMC documentation for Health Authorities
- Ensure technical congruency and regulatory compliance
- Meet e-publishing requirements and project timelines
- Represent Global Regulatory CMC on cross-functional teams
- Maintain collaborative partnerships with key stakeholders
- Lead Health Authority interactions and negotiations
- Prepare briefing books and risk mitigation plans
- Act as the primary contact for the FDA
- Provide strategic advice through specialized assignments
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Competitive Pay
- Market-competitive base salary
Bonuses & Incentives
- Attractive incentive program
Retirement Plans
- Modern company pension scheme
Childcare
- Childcare facilities
Learning & Development
- Learning and development options
Career Advancement
- Worldwide career opportunities
Other Benefits
- Recruitment process adjustments
- Disability representative involvement
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Associate Director, Regulatory Affairs CMC(m/w/x)
Leading global CMC submission planning and authoring for diverse pharmaceutical projects. Minimum 8 years regulatory or pharmaceutical experience required. On-site childcare facilities.
Requirements
- Science degree or equivalent
- Minimum 8 years regulatory or pharmaceutical experience
- Knowledge in regulatory submission and CMC issues
- Ability to critically evaluate scientific data
Tasks
- Drive global CMC regulatory strategies for diverse projects
- Lead all global CMC submission planning and authoring
- Coordinate and review technical submission documentation
- Identify and resolve content or quality issues
- Negotiate delivery of technical source documents
- Author high-quality CMC documentation for Health Authorities
- Ensure technical congruency and regulatory compliance
- Meet e-publishing requirements and project timelines
- Represent Global Regulatory CMC on cross-functional teams
- Maintain collaborative partnerships with key stakeholders
- Lead Health Authority interactions and negotiations
- Prepare briefing books and risk mitigation plans
- Act as the primary contact for the FDA
- Provide strategic advice through specialized assignments
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Competitive Pay
- Market-competitive base salary
Bonuses & Incentives
- Attractive incentive program
Retirement Plans
- Modern company pension scheme
Childcare
- Childcare facilities
Learning & Development
- Learning and development options
Career Advancement
- Worldwide career opportunities
Other Benefits
- Recruitment process adjustments
- Disability representative involvement
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Novartis
Industry
Pharmaceuticals
Description
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Not a perfect match?
- Novartis Pharmaceutical Manufacturing GmbH
Regulatory Affairs Associate Director, CMC(m/w/x)
Full-timeOn-siteExperiencedSchaftenaufrom 78,383.9 / year - Novartis
Manager, Regulatory Affairs CMC(m/w/x)
Full-timeOn-siteManagementSchaftenaufrom 65,605.54 / year - Novartis Pharmaceutical Manufacturing GmbH
Drug Product Project Leader – Associate Director Science & Technology(m/w/x)
Full-time/Part-timeOn-siteSeniorSchaftenaufrom 78,383.9 / year - Novartis Pharmaceutical Manufacturing GmbH
Technical Transfer Lead(m/w/x)
Full-time/Part-timeOn-siteExperiencedSchaftenaufrom 65,605.54 / year - Novartis Pharmaceutical Manufacturing GmbH
R&D Quality Lead(m/w/x)
Full-timeOn-siteExperiencedSchaftenaufrom 78,383.9 / year