Manufacturing Quality Operations Support Associate
Manufacturing Quality Operations Support Associate
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Job Description
Use Your Power for Purpose
Every 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 Achieve
In this role you will:
- Approve planned alarms and work orders (WO)
- Perform Compliance Walkthroughs
- Aseptic gowning occasionally
- Support site regulatory inspections
- Lead & suggest Continuous Improvements (CI) initiatives to improve safety and processes and successfully utilize IMEX tools and the one best way philosophy.
- Review/approve new/existing procedures (SOPs MBRs Job Aids etc.) in Documentum to ensure proposed critical changes to procedures and/or processes are completed/documented appropriately.
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
- Experience in the pharmaceutical industry and Quality administered systems
- Sound knowledge of current Good Manufacturing Practices (part of GxP)
- Ability to work effectively in a team environment both within ones own team and interdepartmental teams
- Effective written and oral communication skills
Bonus Points If You Have (Preferred Requirements)
- Experience at a manufacturing site.
- Experience with review/approval of new/existing procedures (SOPs MBRs Job Aids etc.) in Documentum
- Knowledge of electronic systems including Trackwise Documentum/PDOCs SAP gLIMS Microsoft Office electronic batch records systems quality management systems.
- Strong problem-solving skills
- Ability to work independently and as part of a team
- Excellent time management and multitasking abilities
PHYSICAL/MENTAL REQUIREMENTS
- Standing/sitting for periods of more than one (1) hour.
NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS
- This role may occasionally require on-call after hours and weekend support.
OTHER JOB DETAILS
Last Date to Apply for Job: 7/28/25
Work Location Assignment: On site
Relocation support available
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
Pfizer 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 providers 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 Eligibility
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 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.
Required Experience:
IC
Employment Type
Full-Time
