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The Role
The role involves providing regulatory support for registration applications, managing product lifecycle issues, coordinating submissions, and ensuring compliance with health regulatory frameworks.
Summary Generated by Built In
Use Your Power for Purpose
We are committed to delivering medicines to the world with greater speed, without compromising on excellence and integrity. Navigating both local and global regulations is crucial, and the dynamic regulatory landscape demands innovative thinking and meticulous attention to detail. Your unwavering dedication and specialized knowledge will play a pivotal role in broadening and hastening patient access to Pfizer's medicines and vaccines.
What You Will Achieve
In this role, you will:
- M1 dossier components (local document authoring and/or coordination)
- Simple local only HA query responses,
- Provide support for general x-functional activities to country Regulatory teams for tenders, out-of-stock reporting, Annual Product Quality Review, risk minimization plans, and coordination of regulatory input for launch planning.
- Identification of regulatory requirements (for the in-scope submission categories defined),
- Authoring, delivery and/or coordination of local, submission-ready documents and
- The quality review/approval of the Dossier provided by Hub Submission/Dossier Managers (for the in-scope submission categories defined).
Here Is What You Need (Minimum Requirements)
Bonus Points If You Have (Preferred Requirements)
Work Location Assignment: Hybrid
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Regulatory Affairs
We are committed to delivering medicines to the world with greater speed, without compromising on excellence and integrity. Navigating both local and global regulations is crucial, and the dynamic regulatory landscape demands innovative thinking and meticulous attention to detail. Your unwavering dedication and specialized knowledge will play a pivotal role in broadening and hastening patient access to Pfizer's medicines and vaccines.
What You Will Achieve
In this role, you will:
- Be responsible for providing operational regulatory support to the International country and/or cluster Regulatory teams.
- Work across portfolio phases from initial registration applications, lifecycle management through to product withdrawal to support numerous regulatory activities that include but are not limited to;
- M1 dossier components (local document authoring and/or coordination)
- Simple local only HA query responses,
- Provide support for general x-functional activities to country Regulatory teams for tenders, out-of-stock reporting, Annual Product Quality Review, risk minimization plans, and coordination of regulatory input for launch planning.
- Partner closely with the Country Regulatory Strategist and Hub Submission/Dossier Managers to enable timely, high-quality submissions and sustained compliance. This includes but is not limited to:
- Identification of regulatory requirements (for the in-scope submission categories defined),
- Authoring, delivery and/or coordination of local, submission-ready documents and
- The quality review/approval of the Dossier provided by Hub Submission/Dossier Managers (for the in-scope submission categories defined).
Here Is What You Need (Minimum Requirements)
- B.Pharm/BA/BS with 2+ years of experience
- Demonstrated experience in regulatory affairs or in a regulated industry
- In-depth knowledge of the current health regulatory framework for drug regulatory procedures
- Strong problem-solving skills, attention to detail, and a quality and compliance orientation
- Excellent verbal and written communication skills, and fluent in English
- Proficient in MS Office Suite
Bonus Points If You Have (Preferred Requirements)
- A Master's degree along with relevant pharmaceutical experience
- Familiarity with electronic submission processes and regulatory information management systems
- Ability to work effectively in a fast-paced, dynamic environment
- Strong interpersonal skills and the ability to work collaboratively with cross-functional teams
- Excellent organizational and time management skills
- Ability to adapt to changing priorities and manage multiple tasks simultaneously
- Strong analytical skills and the ability to interpret complex regulatory guidelines and requirements
- 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
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Regulatory Affairs
Skills Required
- B.Pharm/BA/BS with 2+ years of experience
- Demonstrated experience in regulatory affairs or in a regulated industry
- In-depth knowledge of health regulatory framework for drug regulatory procedures
- Strong problem-solving skills and attention to detail
- Excellent verbal and written communication skills, fluent in English
- Proficient in MS Office Suite
What the Team is Saying
Daniel
Diagnostics Launch Lead
Anna
R&D Privacy Steward
Esteban
Specialist
Pfizer Compensation & Benefits Highlights
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Parental & Family Support — U.S. materials describe up to 26 weeks of parental leave (including up to 12 paid non‑medical weeks), with phased return‑to‑work plus fertility, adoption, and surrogacy financial support, backup care, lactation support, and caregiver leave. These offerings indicate depth in family‑building benefits and day‑to‑day caregiver resources.
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Healthcare Strength — Core programs commonly include medical, prescription drug, dental, vision, mental‑health/EAP resources, disability insurance, preventive health programs, and free or reduced‑cost vaccinations. Voluntary Benefit Extras and wellness resources broaden coverage and access.
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Retirement Support — Career pages and postings note a 401(k) with company matching plus an additional company retirement savings contribution in some plans. Company materials also reference financial‑planning education and colleague‑directed retirement funds.
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The Company
What We Do
Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.
Why Work With Us
We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.
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Pfizer Offices
Hybrid Workspace
Employees engage in a combination of remote and on-site work.
Typical time on-site:
Not Specified
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