Use Your Power for Purpose
At Pfizer, we are committed to bringing medicines to the world with speed, without compromising on excellence and integrity. Navigating the ever-changing regulatory environment requires forward thinking and meticulous attention to detail. Adhering to both local and global regulations is crucial. Your dedication and expertise are vital in expanding and accelerating patient access to Pfizer's innovative medicines and vaccines. By maintaining our high standards and ethical practices, we ensure that patients receive the best possible care. Join us in our mission to make a meaningful impact on global health.
What You Will Achieve
As a Senior Associate in Regulatory Chemistry, Manufacturing, and Control Strategy at Pfizer, you will play a critical role in developing and implementing regulatory strategies for both small and large molecule pharmaceuticals. Your expertise will be essential in preparing regulatory submissions and liaising with health authorities to ensure compliance with global requirements.
- Contribute to project completion and manage time to meet targets.
- Support assembly of Chemistry, Manufacturing and Control (CMC) information for global regulatory submissions.
- Actively contribute to cross-functional initiatives to mitigate risks.
- Ensure compliance with submission standards, procedures, and policies.
- Prepare and finalize Global Regulatory Strategy Documents and Clinical Data Request (CTD) sections for submissions.
- Maintain core dossiers and coordinate responses to deficiency letters.
- Review and apply regulatory guidelines for renewals.
- Recommend solutions and escalate issues with significant impact.
- Independently manage projects and execute strategies with minimal oversight.
- Collaborate with cross-functional teams to support regulatory strategies.
Here Is What You Need (Minimum Requirements)
- A BA /BS with 2+ years of experience, an MBA or MS with 0+ years of experience, an associate degree with 6+ years of experience, or a high school diploma (or equivalent) with 8+ years of relevant experience.
- Demonstrated commitment to scientific and regulatory integrity and quality compliance
- Sound understanding of regulatory processes and requirements for defined market(s) and able to interpret and apply to projects
- Ability to learn and navigate tracking/change control systems, compliant and consistent use of systems and willingness to support others in system use
- Demonstrated integrity in decision making on regulatory issues in line with company values
- Ability to contribute to effective teams and implement change and make decisions to resolve problems in standard situations
- Competent working knowledge of computer-based systems, such as Microsoft Office, controlled documentation systems
Bonus Points If You Have (Preferred Requirements)
- Pharmaceutical industry experience
- Experience in regulatory CMC strategy for both small and large molecule pharmaceuticals
- Proficiency in regulatory information management systems.
- Strong analytical and problem-solving skills
- Project management experience
- Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use
Work Location Assignment: Hybrid
EEO (Equal Employment Opportunity) & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, or disability.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.
Regulatory Affairs