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Senior Quality Assurance Associate

Job in West Greenwich, Kent County, Rhode Island, 02817, USA
Listing for: Planet Pharma
Full Time position
Listed on 2026-01-11
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control / Manager, QA Specialist / Manager
Salary/Wage Range or Industry Benchmark: 31 - 32 USD Hourly USD 31.00 32.00 HOUR
Job Description & How to Apply Below
Location: West Greenwich

Quality Assurance Senior Associate (GMP/Floor)

Location:

West Greenwich, RI

Base pay range: $31.00/hr - $32.00/hr

Position Overview

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, 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 reject materials.
  • 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 elevate 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.
Preferred Qualifications
  • Bachelor’s Degree in a relevant field (e.g., Life Sciences)
  • Minimum of 2 years of experience in Quality or Manufacturing, with exposure to F&E-related activities.
  • 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.
Seniority Level

Mid‑Senior level

Employment Type

Contract

Job Function

Quality Assurance

Benefits
  • Medical insurance
  • Vision insurance
  • 401(k)
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Position Requirements
10+ Years work experience
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