
Senior Manager, Regulatory Affairs - CMC
- Hertfordshire
- Permanent
- Full-time
- Lead and manage CMC-regulatory activities across various development and marketed products, ensuring compliance and regulatory risk mitigation.
- Collaborate closely with cross-functional teams including Integrated Project Teams (IPTs) and CMC to drive license submissions and approvals.
- Develop and execute CMC-regulatory strategies and oversee the preparation of key regulatory documents, including Module 3 sections.
- Provide expert advice on CMC-regulatory issues and quality guidelines to stakeholders and project teams.
- Support growth market submissions and manage post-approval changes in liaison with affiliates and distributors.
- Continuously evaluate and improve CMC-regulatory processes to enhance efficiency and patient-centric approaches.
- Proven track record in CMC-regulatory affairs within the pharmaceutical industry.
- Strong understanding of regulatory guidelines and quality standards related to drug substance and drug product development.
- Excellent leadership and stakeholder management skills, with the ability to handle multiple projects simultaneously.
- Experience working within cross-functional teams and navigating complex regulatory environments.
- Strategic mindset with a passion for innovation and patient-focused healthcare solutions.
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