Senior QA Associate - Plant

GTT, LLCWest Greenwich, RI

$25 - $25 / hour

Apply with Sonara

Automate your job search with Sonara.

Submit 10x as many applications with less effort than one manual application.¹

Reclaim your time by letting our AI handle the grunt work of job searching.

We continuously scan millions of openings to find your top matches.

Overview

Remote

On-site

Compensation

$25-$25/hour

Job Description

QA Senior Associate - Plant

Location: West Greenwich, RI

Onsite Flexibility: Onsite

Contract Details

Position Type: Contract
Contract Duration: 12 months
Pay Rate: $25.00 $27.00 / Hour (USD)
Shift / Schedule: Administrative Shift | 6:45 AM 3:15 PM (with 30-minute meal break)
Work Authorization: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

Job Summary

In this critical role, you will serve as a Plant Quality Assurance (PQA) professional, providing on-the-floor quality oversight for Facilities and Engineering (F&E), Process Development, Incoming Quality Assurance (IQA), and Manufacturing operations. This position requires close collaboration with cross-functional teams to ensure that all activities within bulk drug substance operations adhere to cGMP and other regulatory requirements.

Key Responsibilities

Provide quality oversight for F&E, IQA Warehouse areas (including Incoming Inspections and the Raw Material Sampling Lab), and Process Development Laboratories.
Ensure facilities, equipment, materials, processes, and products comply with cGMP standards and other applicable regulatory requirements.
Review and approve work orders and job plans within Maximo.
Review logbooks (paper-based and electronic), particle-generating forms, pest control sighting forms, and periodic pest control (monthly/quarterly) reports, RT reports, and other GMP documentation.
Review and approve Manufacturing Execution System (MES) records, including EBRs and ESPs.
Handling of rejected materials.
Review/Approve Delta V Audit Trail entries.
Ensure that any deviations from established procedures are properly documented according to approved processes.
Communicate and collaborate effectively across departments (PQA, PD, IQA, F&E, and Manufacturing) to ensure completion of assigned tasks.
Complete required training assignments to maintain compliance and readiness for task execution.
Proactively identify and escalate quality, compliance, or safety risks to management.
Maintain a presence in cleanroom areas (~25% of shift time), including proper gowning and adherence to aseptic practices.

Required Skills

Ability to prioritize and navigate ambiguity, with minimal oversight, in a fast-paced environment.
Experience collaborating within and across functional areas, with a strong focus on customer service and partnership.
GMP experience (either MFG or QA).

Preferred Skills

Strong understanding of cGMP principles and regulatory expectations.
Demonstrated experience utilizing enterprise systems such as Maximo, OEFM, MES, and Veeva Vault (CDOCS/DQMS) to support quality oversight, documentation management, and manufacturing execution processes.
Proficient in Microsoft Office applications, including Outlook, Word, Excel, PowerPoint, and Teams.
Excellent written and verbal communication skills.
Experience collaborating within and across functional areas, with a strong focus on customer service and partnership.
Demonstrated ability to make sound decisions in a dynamic, fast-paced environment.
Ability to prioritize and navigate ambiguity, with minimal oversight, in a fast-paced environment.

Education Requirements

High school diploma / GED + 4 years of work experience, OR
Associate degree + 2 years of work experience, OR
Bachelor's degree + 6 months of work experience, OR
Master's degree
Bachelor's degree in a relevant field (e.g., Life Sciences) preferred.

Required Experience

Minimum of 2 years of experience in Quality or Manufacturing, with exposure to F&E-related activities (preferred).

Work Environment / Physical Requirements

Maintain a presence in cleanroom areas (~25% of shift time), including proper gowning and adherence to aseptic practices.

Important Notes

Red Flag: No GMP experience (biopharmaceutical or pharmaceutical) will disqualify a candidate.
Interview Process: Video Conference Call with Hiring Manager.

Benefits

Medical, Vision, and Dental Insurance Plans
401k Retirement Fund

About GTT

GTT is a minority-owned staffing firm and a subsidiary of Chenega Corporation, a Native American-owned company in Alaska. We highly value diverse and inclusive workplaces and support Fortune 500 organizations across banking, financial services, technology, life sciences, biotech, utilities, and retail sectors throughout the U.S. and Canada.

Job Number: 26-14068 Industry: Manufacturing & Operations

#LI-Onsite #gttic

Automate your job search with Sonara.

Submit 10x as many applications with less effort than one manual application.

Apply with Sonara Apply manually

FAQs About Senior QA Associate - Plant Jobs at GTT, LLC

What is the work location for this position at GTT, LLC?

This job at GTT, LLC is located in West Greenwich, RI, according to the details provided by the employer. Some roles may also include multiple work locations depending on the requirement.

What pay range can candidates expect for this role at GTT, LLC?

Candidates can expect a pay range of $25–$25 per hour for this role.

What employment applies to this position at GTT, LLC?

The employer has not provided this information. This may be discussed during the hiring process.

What is the process to apply for this position at GTT, LLC?

You can apply for this role at GTT, LLC either through Sonara's automated application system, which helps you submit applications 10X faster with minimal effort, or by applying manually using the direct link on the job page.