Quality Assurance Associate

Use Your Power for PurposeEvery day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. Your role is crucial in maintaining this commitment and driving forward our mission to improve patient outcomes.What You Will AchieveIn this role, you will:Execute on defined and established procedures, work instructions and templatesProcess documents in electronic Document Management SystemAnswer basic questions and send routine notificationsIssue and reconcile batch records, forms, and logbooksMaintain and distribute documents to Controlled Document LocationsBack-up the Records Management job function as requiredResponsible for receiving and logging GMP records, cataloging, physical or electronic filing, and retrieval as neededWorks with GMP personnel submitting and retrieving records to ensure records are maintained and tracked in a compliant manner and are readily retrievable.Participates in cross-functional teams to implement, update, or upgrade systems or processes related to the management of GMP records.Supports GMP regulatory audits and inspections ensuring timely retrieval of both physical and electronic records.Scans and digitizes GMP records and verifies as true copies.Performed reconciliation of completed records issued for GMP activities.Collects and assists with reporting on relevant metrics.Works with off-site storage facilities to ensure compliant submission and retrieval of GMP records.Contribute to milestones related to specific projects.Participates in continual improvement activities within Document Control and GMP Records management.Here Is What You Need (Minimum Requirements)Bachelor's degree with any years of experience, or an Associate's degree with 3 years of relevant experience, or a high school diploma (or equivalent) and 6 years of relevant experienceExperience in the pharmaceutical industry and Quality administered systemsSound knowledge of current Good Manufacturing Practices (part of GxP)Ability to work effectively in a team environment, both within one's own team and interdepartmental teamsEffective written and oral communication skillsBonus Points If You Have (Preferred Requirements)Experience at a manufacturing site.Managing and writing deviations, Change Control and CAPAExperience in production batch record issuance, reconciliation, investigation of non-conformance, root cause analysis and change control managementStrong problem-solving skillsAbility to work independently and as part of a teamExcellent time management and multitasking abilities  PHYSICAL/MENTAL REQUIREMENTSN/ANON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS N/AWork Location Assignment: On PremiseThe annual base salary for this position ranges from $66,500.00 to $110,900.00. In addition, this position is eligible for participation in Pfizer’s 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 life’s 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.Sunshine ActPfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.EEO & Employment EligibilityPfizer 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, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. Pfizer endeavors to make /careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email disabilityrecruitment@. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.Quality Assurance and Control

Created: 2025-11-24