Top 7 Quality assurance associate Jobs in Coventry Ri

Quality Assurance Senior Associate
Aequor Technologies LLC —West Greenwich, RI
- Contract
- Microsoft Excel
- Microsoft Outlook
- Customer service
Quick Apply
QA Associate Documentation I
Boston Scientific —Coventry, RI
- $47,200 - $89,700 a year
- Full-time
- Engineering
- Neurology
- In-person
Associate Quality Control
Amgen —West Greenwich, RI
- $62,571.90 - $84,656.10 a year
- Monday to Friday
- Mid-level
- High school diploma or GED
- Organizational skills
- Disability insurance
- Health insurance
3d
Quality Assurance Associate I
CEDENT —Cumberland, RI
- Full-time
- Mid-level
- Communication skills
Quality Associate
Composite Energy Technologies —Bristol, RI
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Health insurance
- Dental insurance
Quick Apply
Senior Associate Manufacturing Deviation Owner Environmental and Contamination Control
Amgen —West Greenwich, RI
- $86,048.05 - $116,417.95 a year
- Bachelor of Science
- Master's degree
- High school diploma or GED
- Disability insurance
- Health insurance

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Environmental Engineer / Scientist - Air Quality (Mid-Level)
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Bachelor's or master’s of science degree in related discipline. Ability to work in both office and industrial manufacturing environments.
$70,000 - $100,000 a year
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2d
QA Operations Associate I
American Regent, Inc. —New Albany, OH
Achieve and maintain packaging line and inspection room clearance qualification. Perform room, area and equipment clearances.

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Quality Assurance Senior Associate

Aequor Technologies LLC -
West Greenwich, RI

Quick Apply

Job Details

Contract

Qualifications

Raw material quality management
Microsoft Excel
Quality records maintenance
Microsoft Outlook
Maximo
Laboratory document review
Document control experience within pharmaceutical industry
Customer service
Enterprise software
GMP
Cleanroom protocols
Mid-level
Manufacturing process inspections
Bachelor's degree
Quality risk management
Task prioritization
Cleanroom gowning procedures
Decision making
Quality assurance experience within pharmaceutical industry
Compliance documentation
Microsoft Teams
Regulatory/legal compliance standards in production
Cleanroom experience
Collaboration with manufacturing teams
Production batch record review
2 years
Quality control records management
Communication skills
Cross-functional communication
Pharmaceutical manufacturing facility experience

Full Job Description

Note:
100% onsite ARI
Location:
Onsite – West Greenwich, RI
Schedule:
Administrative Shift | 8:30 AM – 5:00 PM (with 30 minute meal break)
Contract Length:
12 months with potential for extension

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, 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 reject 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.

Preferred Qualifications:

Bachelor's Degree in a relevant field (e.g. Life Sciences)
Minimum of 2 year 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.

#TechRV

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Refine Your Search

quality assurance associate jobs in coventry ri

Quality Assurance Senior Associate

QA Associate Documentation I

Associate Quality Control

Quality Assurance Associate I

Quality Associate

Senior Associate Manufacturing Deviation Owner Environmental and Contamination Control

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