Senior Regulatory Associate
Pfizer Inc., Tadworth, Reigate and Banstead
Senior Regulatory Associate
Salary not available. View on company website.
Pfizer Inc., Tadworth, Reigate and Banstead
- Full time
- Permanent
- Onsite working
Posted 1 day ago, 4 Oct | Get your application in today.
Closing date: Closing date not specified
Job ref: afbab44d8d174fb592c8b888b0a20387
Location ref: Tadworth, Reigate and Banstead
Full Job Description
Job DescriptionJoin Our Team as a Regulatory Affairs Specialist!Are you ready to make a difference in the world of healthcare? At Pfizer, we are dedicated to transforming patients' lives through innovative solutions. As a Regulatory Affairs Specialist, you will play a crucial role in ensuring our products meet the highest standards of safety and efficacy. Join us in our mission to create breakthroughs that change lives!Job Responsibilities Deliver Regulatory Strategy: Collaborate with cross-functional teams to provide expert regulatory advice and information. Manage Applications: Oversee New Registration, Marketing Authorization (MA) Variation, and MA Renewal Applications. Engage with Authorities: Respond promptly to queries from National Regulatory Authorities (NRA) and seek clarification when needed. Support Clinical Development: Partner with national Regulatory Authorities and Clinical Trials Regulatory Strategy Execution (CTRSE) to support strategic clinical activities. Maintain
Regulatory Databases: Ensure accurate and up-to-date records of regulatory activities. Safeguard Compliance: Manage updates to packaging and prescribing information components. Contribute to Good Regulatory Practice: Support the development of regulatory best practices within the team. Lead Personal Development: Take charge of your growth and development in the regulatory field.Qualifications & Skills Educational Background: Life sciences or chemistry graduate to honors level or equivalent; Master's degree, Post Graduate Diploma, or PhD preferred. Professional Qualifications: Relevant qualifications such as an MSc in Regulatory Affairs are desirable. Experience: Proven track record in Regulatory Affairs for Human Medicinal Products. Technical Skills: Strong computer literacy and excellent written and verbal communication skills. Analytical Thinking: Demonstrated strength in analytical problem-solving.Working ConditionsAll applicants must have the relevant authorization to live and work in
the UK. We foster a trusting and flexible workplace culture that encourages work-life harmony, allowing you to be your best self.Why Join Pfizer? Growth Opportunities: We are committed to your professional development and offer various pathways for growth. Diversity & Inclusion: We celebrate a diverse workforce and believe it is crucial to our success. Join a culture that empowers everyone. Disability Confident Employer: We are proud to support individuals with unique abilities and will make reasonable adjustments to support your journey with us.Let's start the conversation about how you can contribute to our mission at Pfizer. Together, we can unleash the power of our people and make a lasting impact on the lives of patients around the world!