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 3 days ago, 2 Oct | Get your application in today.

Closing date: Closing date not specified

Job ref: 02dbf67f8678446bb4bc0fc5d44cb979

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 SummaryUnder the guidance of experienced leaders, you will conduct strategic regulatory activities for assigned products and markets. Your work will be essential in obtaining and maintaining Marketing Authorizations and supporting Clinical Trial Applications, all while aligning with our business goals and legal requirements.Key Responsibilities Deliver Regulatory Strategy: Provide expert regulatory advice to cross-functional teams and meet customer requests. Manage Applications: Oversee New Registration, Marketing Authorization Variations, and Renewal Applications.

Engage with Authorities: Respond promptly to queries and requests from National Regulatory Authorities (NRA). Maintain Regulatory Databases: Ensure accurate and up-to-date records of all regulatory activities. Support Clinical Development: Collaborate with national Regulatory Authorities and Clinical Trials Regulatory Strategy Execution (CTRSE). Contribute to Good Regulatory Practice: Uphold compliance in packaging and prescribing information updates. Lead Personal Development: Take charge of your growth and contribute to the development of the Regulatory Group.Qualifications & Skills Education: Life sciences or chemistry graduate (honors level or equivalent); Master's degree or PhD preferred. Experience: Proven track record in Regulatory Affairs for Human Medicinal Products. Technical Skills: Computer literacy and excellent analytical thinking. Communication: Strong written and verbal communication skills.All applicants must have the relevant authorization to live and work in the UK.Why

Join Pfizer?At Pfizer, we believe in a flexible workplace culture that promotes work-life harmony. We are committed to creating an environment where everyone can thrive and be their best selves. Here's what you can expect: Growth Opportunities: We support your professional development and encourage continuous learning. Diversity & Inclusion: We celebrate diverse backgrounds and perspectives, fostering a culture of empowerment. Disability Confident: We are proud to be a Disability Confident Employer, ensuring support for all applicants.Let's Start the Conversation!Join us in our journey to enhance health outcomes and improve patient experiences. Your unique skills and passion can help us achieve our mission. Together, we can make a difference!To learn more about our commitment to innovation and our digital transformation strategy, explore the opportunities at Pfizer.

Direct job link

https://www.jobs24.co.uk/job/senior-regulatory-associate-127500092