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Pfizer Regulatory Affairs Jobs (NOW HIRING)

Pfizer

Field Medical Outcomes Director

Three Rivers, MI · On-site

Represents Pfizer Oncology Medical Affairs leadership with clinical/professional associations and ... These laws and regulations require Pfizer to provide government agencies with information such as a ...

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How much do pfizer regulatory affairs jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for pfizer regulatory affairs in the United States is $39.57, according to ZipRecruiter salary data. Most workers in this role earn between $31.73 and $46.88 per hour, depending on experience, location, and employer.

How does the Regulatory Affairs team at Pfizer typically collaborate with other departments during the drug approval process?

At Pfizer, Regulatory Affairs professionals work closely with cross-functional teams, including Research & Development, Clinical, Quality Assurance, and Legal, to ensure that all regulatory submissions meet global standards. They coordinate timelines, review scientific data, and help interpret regulatory guidelines for the team. Effective communication and teamwork are essential, as Regulatory Affairs often act as the liaison between internal teams and external regulatory agencies. This collaborative approach helps streamline the approval process and maintain compliance across all stages of product development.

Is Pfizer Regulatory Affairs high paying?

Pfizer Regulatory Affairs professionals typically earn competitive salaries that are above average for the industry, reflecting the specialized knowledge and skills required in regulatory compliance, documentation, and communication with authorities. Compensation can vary based on experience, location, and level of responsibility, with senior roles often offering higher pay and additional benefits.

What is a Pfizer Regulatory Affairs professional?

Pfizer Regulatory Affairs professionals are experts who ensure that Pfizer's products meet all regulatory requirements in each country where they are sold. They work closely with governmental agencies to obtain approval for new drugs, maintain compliance for existing products, and keep up with changing regulations. Their role is crucial in facilitating the timely and safe introduction of medicines to the market. They also provide strategic guidance throughout the product lifecycle to help Pfizer navigate complex regulatory environments.

What are the key skills and qualifications needed to thrive as a Regulatory Affairs professional at Pfizer, and why are they important?

To thrive as a Regulatory Affairs professional at Pfizer, you need a strong background in life sciences, regulatory guidelines, and pharmaceutical compliance, typically supported by a relevant degree. Familiarity with regulatory submission systems, document management tools, and certifications such as RAC (Regulatory Affairs Certification) are commonly required. Excellent attention to detail, project management, and effective communication skills set top candidates apart in this role. These skills ensure timely product approvals, adherence to global regulations, and successful collaboration across departments, which are critical for bringing safe and effective medicines to market.

What is the difference between Pfizer Regulatory Affairs vs Pfizer Regulatory Operations?

AspectPfizer Regulatory AffairsPfizer Regulatory Operations
Primary FocusDeveloping and managing regulatory strategies, preparing submissions, ensuring compliance with regulationsImplementing and supporting regulatory processes, managing documentation, and coordinating submissions
Required CredentialsBachelor's or higher in life sciences, regulatory affairs certification often preferredBachelor's in life sciences, regulatory or project management experience beneficial
Work EnvironmentOffice-based, cross-functional collaboration with R&D, legal, and compliance teamsOffice-based, operational support within regulatory teams, coordination with external agencies

Pfizer Regulatory Affairs focuses on strategic regulatory planning and submission preparation, while Pfizer Regulatory Operations handles the implementation and management of regulatory processes. Both roles require similar educational backgrounds and work in collaborative, office-based environments within the pharmaceutical industry.

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Pfizer Regulatory Affairs jobs near you
Infographic showing various Pfizer Regulatory Affairs job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 87% Full Time, 9% Part Time, and 3% Contract. Highlights an 90% Physical, 4% Hybrid, and 6% Remote job distribution, with an average salary of $82,307 per year, or $39.6 per hour.

Pharma Labeling Regulatory Affairs Analyst / Remote Work

Pioneer Data

Pearl River, NY • Remote

Contractor

Posted 4 days ago

Job description

Position Details:
Our client, a world-leading Pharmaceutical Company in Pearl River, NY is currently looking for an Pharma Labeling Regulatory Affairs Analyst to join their expanding team.
 
Job Title: Pharma Labeling Regulatory Affairs Analyst / Remote Work
Duration: 10 months contract, extendable up to 48 months
Location: Remote Worker
 
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
 
Job Description:
Pan-Portfolio Strategy & Support Business Analyst
 
Education:
Bachelor’s Degree or equivalent
Advanced academic qualification/degree desired, equivalent relevant professional experience will be considered.
 
Experience and Attributes:
8+ years’ experience in global/multi-national pharmaceutical environment, including direct experience either in Labeling or Regulatory Affairs role.
Experience with Business Analytics required.
Experience with interacting autonomously with leaders and working in a matrix team environment a must.
Experience in interpreting and applying global and local regulatory guidance around labeling/regulatory and associated supportive documentation desirable.
Experience in labeling and/or artwork processes preferred
Demonstrated track record of delivery to time and quality
 
Technical Skills
Proven fluency with use of soft skills and negotiation skills
Ability to transform ambiguous situations/discussions into structured outcomes
Ability to partner with wide range of business stakeholders, crossing multiple divisions across multiple countries/cultures
Proven leadership driving highly complex projects to meet evolving business needs
Ability to manipulate and understand complex data.
Ability to synthesize and communicate complex information and analyses to a variety of audiences in both verbal and written format
Clear and adaptive verbal and written communication skills
Excellent problem-solving capabilities
Strong facilitation and project management skills
Ability to evaluate and diagnose process and systems
Knowledge and experience with labeling or similar tracking systems
Knowledge of XML, regulatory tracking, document management systems, various reporting tools
The preferred candidate will have experience with Pfizer’s labeling intelligence systems (PfLEET, GDMS, PEARL).
This position is responsible for coordinating and supporting to maintenance of the Pfizer’s labeling intelligence interfacing with internal stakeholders to support Pfizer’s labeling portfolio in alignment with business needs and compliance standards.

Specific responsibilities:
Coordinate the labeling universe maintenance process, including analysis and tracking of updates. Ensure regular data quality checks are performed support the resolution of identified issues.
Coordinate the implementation of label tracking strategies throughout the lifecycle of Pfizer’s products including end of label maintenance activities are performed.

Specifications:
This role has expertise in clinical, global and international labeling and/or artwork functions and interdependencies.
The preferred candidate will have experience with Pfizer’s labeling intelligence systems (PfLEET, GDMS, PEARL).