QC Coordinator

Use Your Power for Purpose
Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture, which is both science and risk-based, is flexible, innovative, and customer-oriented. Whether you are engaged in development, maintenance, compliance, or analysis through research programs, your contribution will have a direct impact on patients. Our dedication to quality and safety ensures that we consistently meet the needs of those we serve. By being part of our team, you play a crucial role in maintaining this high standard and making a difference in the lives of patients.
Role Summary
This position supports commercial manufacturing and the QC testing labs by managing the delivery and storage of samples. Sample types may include release test, backups, retains, reference material, assay controls, and stability. Support and maintain retain program as required by regulatory agencies and Boards of Health. Monitoring of environmental chambers is also critical to the storage of the above sample types.
What You Will Achieve
In this role, you will:

• Coordinate receipt and delivery of samples from designated sample ports to QC laboratories or QC cGMP areas and maintain the inventory for retain samples, backup samples and reference material.
• Adhere to Good Manufacturing Practices (cGMP) and proper documentation practices with generating, reviewing, and reconciling department records.
• Utilize sampling plans effectively and report any problems or adverse quality events to the management and Quality Assurance.
• Maintain sample inventories; and monitor and maintain QC Cold storage units. Perform space evaluations for receipt of material.
• Assist in sampling for laboratory control testing, stability testing, and other special purposes.
• Data entry and distribution of inventory reports.
• Participate in on-call program - Be part of the rotation for the on-call program to support critical equipment 24/7.
• Coordinate and maintain Standard Operating Procedures (SOPs) within the Document Management System (DMS).
• Meetings - Represent the functional group at meetings related to projects, investigations or issues.
• Investigations - May attend meetings for investigations.
• Undertake other duties related to Quality Control or special projects as assigned, manage personal time and growth, and participate in process improvement teams.

Other:

• May cross train and provide support for other areas, such as QC Biological Shipping and Receiving, QC Sampling Operations, Solutions Chemistry, and QC Stability Operations

Here Is What You Need (Minimum Requirements)

• High School Diploma or GED.
• Ability to multi-task across various capabilities and functions while managing competing priorities and requirements
• Effective interpersonal and communication skills
• Working knowledge of Microsoft Office applications
• Ability to work effectively in a collaborative team environment

Bonus Points If You Have (Preferred Requirements)

• Familiarity with Quality Tracking Systems
• Experience using common AI tools, including generative technologies such as ChatGPT or 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, including risk management and ethical use
• Biotechnology Certificate
• Labware LIMS Experience
• Experience working in a GMP facility
• IATA and 49 CFR certification

Non-Standard Work Schedule, Travel, or Environment Requirements

• 1st shift, Sunday through Thursday (weekend differential applies)
  Some holiday coverage required

PHYSICAL/MENTAL REQUIREMENTS
Ability to lift up to 50lbs (assisted)
50-75% of time standing and/or walking
OTHER JOB DETAILS
Last Date to Apply for Job: Feb 18, 2026.
Referral Bonus Eligibility: YES
Eligible for Relocation Package: NO
Work Location Assignment: On Premise
The salary for this position ranges from $24,22 to $40,36 per hour. In addition, this position offers eligibility for overtime, weekend, holiday and other pay premiums depending on the work schedule and the Company's policies. 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 | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided applies only to the United States - Massachusetts - Andover location.
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 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 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.
Pfizer endeavors to make www.pfizer.com/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 [email protected] . 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