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QC Coordinator

Job in Andover, Essex County, Massachusetts, 05544, USA
Listing for: Sourceabled
Full Time position
Listed on 2026-02-16
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control / Manager, Quality Technician/ Inspector, QA Specialist / Manager
Salary/Wage Range or Industry Benchmark: 24.22 - 40.36 USD Hourly USD 24.22 40.36 HOUR
Job Description & How to Apply Below

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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