Change Control Specialist

Use Your Power for Purpose

Every day Pfizers unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative always putting the patient first. Your expertise will be vital in implementing documentation systems proposing change control processes and coordinating the review of procedures and forms. Your dedication and hard work have a significant impact on countless lives.

What You Will Achieve

• Prepare and review essential documentation including Good Manufacturing Practices.
• Create and manage change controls change notifications and change authorizations in compliance with company policies and government regulations.
• Implement and propose documentation systems and change control processes coordinating the review of procedures and forms.
• Provide input on quality control procedures and documentation contributing to moderately complex projects and managing time to meet targets.
• Provide technical writing editing and design support creating and updating policies procedures specifications training materials and other technical documents.
• Collaborate with Functional Area and network customers to develop change management plans.
• Facilitate change management pre-meetings and impact assessments working closely with project teams to ensure documents are accurate consistent and meet internal and external regulatory guidelines.

Here Is What You Need (Minimum Requirements)

• Applicant must have a High school diploma (or equivalent) with 8 years of experience or Associates degree with 6 years of experience or Bachelors with 2 years of experience or Masters with any years of relevant experience
• Robust comprehension of cGMP Data Integrity and ALCOA principles
• Proficiency in word processing and document formatting
• Extensive experience with Microsoft Office applications including Word Excel PowerPoint and Visio.

Bonus Points If You Have (Preferred Requirements)

• Relevant pharmaceutical experience
• Demonstrated expertise in technical writing
• Strong project management skills
• Experience with electronic document management systems
• Knowledge of regulatory requirements and guidelines
• Ability to mentor and guide junior colleagues

Physical/Mental Requirements

• Exceptional organizational and communication skills
• Ability to manage multiple tasks and projects simultaneously
• Strong attention to detail and accuracy
• Ability to work independently and as part of a team
• Excellent problem-solving skills
• Strong interpersonal skills

Non-Standard Work Schedule Travel or Environment Requirements

• This role is standard office hours Monday through Friday work schedule

Other Job Details:

• Last day to Apply: Oct 9th 2025
• Eligible for Relocation Assistance: No
• Work Location Assignment: Hybrid

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