Senior Regulatory Strategist for Medications

Pfizer Inc.

Knaphill

On-site

GBP 60,000 - 80,000

Full time

3 days ago

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Job summary

Pfizer Inc. is seeking a Regulatory Affairs Specialist to navigate regulatory landscapes for our medicines.

You will conduct strategic regulatory activities to secure and maintain Marketing Authorizations, support Clinical Trial Applications, and align with business and legal requirements under guidance from experienced leaders. You will advise cross-functional teams, manage registrations and renewals, respond to NRA queries, keep regulatory databases up to date, and contribute to good

Qualifications

Degree in life sciences or chemistry (honors level or equivalent).
Master's degree, Post Graduate Diploma, or PhD preferred.
MSc in Regulatory or similar qualification.
Experience in Regulatory Affairs for Human Medicinal Products.
Strong computer literacy and excellent communication skills.
Proven analytical thinking ability.

Responsibilities

Advise cross-functional teams on regulatory strategy to ensure compliance and success.
Manage New Registration, Marketing Authorization, and Renewal Applications.
Address NRA queries efficiently and accurately.
Maintain regulatory databases up to date and ensure data integrity.
Support Clinical Development with national Regulators and strategists.
Ensure updates to packaging and prescribing information are compliant.
Contribute to Good Regulatory Practice and regulatory process improvements.
Lead personal development and continuous learning.