Your role will be essential in ensuring that our regulatory submissions are prepared, published, tracked, and quality-controlled to meet the highest standards, ultimately supporting patients globally
Job Summary
Your role will be essential in ensuring that our regulatory submissions are prepared, published, tracked, and quality-controlled to meet the highest standards, ultimately supporting patients globally.
You will assist in the preparation, publication, tracking, and quality control of regulatory submissions, ensuring compliance with document management standards and contributing to project tasks and milestones.
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.
Matching Summary
Your role will be essential in ensuring that our regulatory submissions are prepared, published, tracked, and quality-controlled to meet the highest standards, ultimately supporting patients globally.
Skills & Requirements
Must-have
electronic submissions build
regulatory submissions compliance
document management standards
drug development process knowledge
regulated environment coordination
English communication skills
Nice-to-have
project timeline management
stakeholder communications
risk management and problem-solving
organizational and multitasking skills
experience with AI tools
attention to detail and analytical skills
Key Requirements
Bachelor's degree or equivalent experience
Associate's degree with 2 years experience
High school diploma with 6 years experience
Experience in electronic submissions within pharmaceutical industry