Change Control 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

• Oversee quality activities related to change control systems and product change control in collaboration with Regulatory Affairs.
• Support non-manufacturing functions strategic quality planning performance metrics and achieving quality goals and objectives.
• Provide quality-related oversight for various functions ensuring that all processes meet the highest standards.
• Contribute to project tasks and/or milestones organizing your 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.
• Ensure that quality control procedures are robust enough to thoroughly evaluate the organizations products.
• 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.

Here Is What You Need (Minimum Requirements)

• Applicant must have a bachelors degree with 0 years of experience; OR
  an associates degree with 4 years of experience; OR a high school
  diploma (or equivalent) and 6 years of relevant experience
• Familiarity with the use and functionality of eQMS (Veeva Vault) or gQTS (Trackwise)
• 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 core computer software/systems (Word MS Excel PowerPoint etc.)
• Strong organizational skills and attention to detail

Bonus Points If You Have (Preferred Requirements):

• Demonstrated ability to learn and master new applications software
• 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

PHYSICAL/MENTAL REQUIREMENTS

• Mathematical calculation and complex data analysis ability.
• Occasionally lift a computer system and/or instrument up to 50 pounds.
• Use a computer terminal for up to 8 hours per shift work around moving equipment.
• Stand for up to 8 hours sit for up to 8 hours walking climbing stairs responding to visual warning indicators respond to audible warning indicators respond to color or special visual indicators wear specialized protective.

NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS

• Primary work schedule is day shift Monday Friday but evenings weekends and holidays will be required as needed to support manufacturing processes at the Rocky Mount site.
• Must be able to wear proper gowning and PPE in laboratory and manufacturing areas as required to meet GMP and/or OSHA requirements.
• Minimal travel may be required.

Work Location Assignment:On Premise

Last Date To Apply: October 29 2025

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