Centralized Document Management Team Specialist

Use Your Power for Purpose

Everything we do every day is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture rooted in science and risk-based compliance is both flexible and innovative always putting the customer first. Whether your role involves development maintenance compliance or analysis through research programs your contributions will have a direct impact on patient care. Your focus and commitment will be essential in achieving project tasks and goals fostering a collaborative environment for your colleagues. Your hard work and dedication will help Pfizer reach new milestones and make a significant impact on patients worldwide.

What You Will Achieve

• Support GMP document life cycle activities including document control retrieval retention archival and records management.
• Intake document change requests draft documents facilitate stakeholder alignment and drive timely approvals through quality systems.
• Support non-manufacturing functions strategic quality planning performance metrics and achieving quality goals and objectives.
• Provide quality-related oversight for GMP Documents
• Contribute to project tasks and/or milestones organizing work to meet deadlines.
• Learn and apply basic team effectiveness skills within the immediate Work Team.
• Make decisions in limited options to resolve basic problems with limited decision-making authority working under the supervisors direction.
• Work in a structured environment using established procedures and ask for guidance from colleagues.
• Collaborate with Pfizer Digital and the central support team to address enhancements upgrades or issues in the Quality Tracking System.
• Review and approve critical documents such as SOPs Computer Systems validation or verification documentation Change Controls Investigations and Official Computer Systems Lists.

Physical/Mental Requirements:

• This is a Penicilin Facility candidate must NOT be allergic to Penicillin

Here Is What You Need (Minimum Requirements)

• Bachelors degree with any years of experience or an Associates degree with 4 years of relevant experience or a high school diploma (or equivalent) and 6 years of relevant experience
• Familiarity with the use and functionality of Veeva Vault and Documentum
• Ability to work as part of a team in a cross-site support model with colleagues of diverse backgrounds
• Makes decisions that require choosing between limited options to resolve problems basic in their complexity
• Good communication skills asks questions and checks for understanding
• Experience with Laboratory Information Management System Word MS Excel Quality Tracking System
• Strong organizational skills and attention to detail

Bonus Points If You Have (Preferred Requirements):

• Demonstrated ability to learn and master new applications software
• Experience in conducting and documenting manufacturing incident or customer complaint investigations
• Knowledge of regulatory requirements and quality standards in the pharmaceutical industry
• Strong problem-solving skills and the ability to think critically
• Ability to work independently and as part of a team
• Excellent written and verbal communication skills
• Proficiency in data analysis and reporting
• Strong interpersonal skills and the ability to build effective working relationships
• Adaptability and flexibility in a fast-paced environment
• Experience using common AI tools including generative technologies such as 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 includingrisk management and ethical use

Other Job Details:

• Working hours: 7 am - 3:30 pm
• Last day to apply: October 27th 2026.
  

The annual base salary for this position ranges from $68600.00 to $114300.00. In addition this position is eligible for participation in Pfizers Global Performance Plan with a bonus target of 7.5% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of lifes moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution paid vacation holiday and personal days paid caregiver/parental and medical leave and health benefits to include medical prescription drug dental and vision coverage. Learn more at Pfizer Candidate Site U.S. Benefits (). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa FL or any location outside of the United States.

Relocation assistance may be available based on business needs and/or eligibility.

Candidates must be authorized to be employed in the U.S. by any employer.

U.S. work visa sponsorship (such as TN O-1 H-1B etc.) is not available for this role now or in the future.

To learn more about acceptable and prohibited uses of AI during the recruitment process please review our candidate AI-use guidelines available onPfizer Careers.

Quality Assurance and Control