Quality Associate Level 2- Second Shift
Planet Pharma Group · planet-pharma.com
EastonEntry level2+ yrs
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The job in short
An entry-level Specialist / Analyst role at Planet Pharma Group in Easton, asking for 2+ years of experience. Skills mentioned: Warehouse, Compliance.
WarehouseCompliance
Details
- Found
- 6 d ago · posted 2026-11-04
- Location
- easton, Pennsylvania
Full description
Quality Associate II (Cleanroom & GMP Environment)
Overview
Our client is seeking a Quality Associate II to support quality assurance activities within a GMP-regulated warehouse and cleanroom environment. This role is responsible for material inspection, sampling, quality documentation, and compliance activities while ensuring adherence to GMP standards and client requirements.
Responsibilities
• Perform material inspections, sampling, and quality assessments for incoming and outgoing products.
• Review inventory, shipping, and receiving documentation for accuracy and compliance.
• Document deviations, discrepancies, investigations, and quality events within quality systems.
• Support GMP cleanroom operations, including adherence to gowning and contamination control procedures.
• Collaborate with Operations, Inventory, and Quality teams to resolve quality issues and manage non-conforming materials.
• Participate in continuous improvement and compliance initiatives.
Qualifications
• High School Diploma or GED required.
• 2+ years of Quality Assurance, Quality Control, or Quality experience in a GMP-regulated environment.
• Required experience working in a cleanroom environment.
• Required experience performing material sampling activities.
• Experience within pharmaceutical, biotech, medical device, or other highly regulated industries preferred.
• Familiarity with quality management systems, deviation investigations, and GMP documentation.
• Strong attention to detail, organization, and communication skills.
Key Skills
Quality Assurance * Quality Control * GMP Compliance * Cleanroom Operations * Material Sampling * Material Inspection * Documentation Review * Deviation Management * Inventory Control * Warehouse Quality * Regulatory Compliance
Must-Have Requirements
• GMP-regulated industry experience
• Cleanroom experience (clearly demonstrated on resume)
• Material sampling experience (clearly demonstrated on resume)
• Quality Assurance or Quality Control background
• Strong documentation and investigation skills
• Experience working in a warehouse, manufacturing, pharmaceutical, biotech, or medical device environment
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