QC Coordinator
Listed on 2026-02-16
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Quality Assurance - QA/QC
Quality Control / Manager, Quality Technician/ Inspector, QA Specialist / Manager
We strongly encourage applications from individuals with disabilities, including those with autism or other forms of neurodivergence. Our company is committed to diversity, inclusivity, and creating a supportive work environment for all employees.
Job Title:
QC Coordinator
Posted Date:
Feb 11, 2026
Duration: 0 Month, Direct Hire (Full Time)
Shift(s):
09:00 - 18:00
Salary ($): 24.22 - 40.36 per Hourly (compensation based on experience and qualifications)We care about you! Explore Rangam’s benefits information
Rangam is seeking candidates for a Direct Hire role as a QC Coordinator with our client Pfizer , one of the world’s largest pharmaceutical companies. Seeking candidates in Andover, MA or willing to relocate.
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, includingrisk management and ethical use
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
DescriptionRangam is seeking candidates for a Direct Hire role as a QC Coordinator with our client Pfizer , one of the world’s largest pharmaceutical companies. Seeking candidates in Andover, MA or willing to relocate.
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…
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