Quality Assurance Technician

Integrated Resources Inc.; Carlisle (Cumberland County); On-site; USD 50,000 - 70,000; Full time

Job summary

A leading staffing firm seeks a Quality Assurance Technician to ensure product quality and compliance with cGMP standards. The technician will oversee quality activities, assist in investigations, and maintain essential QA systems to support manufacturing processes. Ideal candidates will have strong problem-solving skills and a background in quality operations.

Qualifications

• Familiar with manufacturing and quality operations.
• Ability to prioritize and manage a varied workload.
• Experience in quality assurance practices and compliance.

Responsibilities

• Support manufacturing batch record review activities.
• Prepare and issue production batch records.
• Assist in QA systems development and implementation.

Skills

Quality Oversight

Data Interpretation

Problem Solving

Job description

A Few Words About Us

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-state area's most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy, and Nursing.

Job Description

Our Client is looking for a Quality Assurance Technician

Summary:

• Accountable for activities involved in quality oversight for review and release of finished goods, raw materials, and packaging components, issuance of master batch records, and associated documentation, and tracking of investigations, change controls, and action items related to material release activities.
• Maintains routine programs and processes to ensure high-quality products and compliance with current cGMPs.
• Must be familiar with all aspects of manufacturing and quality operations.
• Ability to effectively prioritize and manage a varied workload is essential.

Responsibilities:

• Support manufacturing batch record review activities.
• Prepare and issue production batch records.
• Perform review and release activities related to finished goods, raw materials, and packaging components.
• Assist in the development and implementation of QA systems and SOPs.
• Initiate and assist in quality investigations of cGMP products as required.
• Generate incident reports, change controls, and CAPA reports as required.
• Perform initiation, maintenance, and closure activities of QA systems such as discrepancies, CAPAs, and change control to support QA operations and ensure SOP compliance.
• Identify, investigate, and report on quality issues.
• Interpret data and communicate results to quality management.
• Maintain effective communication and partnership with operations and materials management departments.
• Perform additional assignments as directed by the Quality Assurance Manager.