CQ Medical · 4 weeks ago
Quality Control Inspector
Avondale, PA
Full-time
Onsite
New Grad, Entry LevelCQ Medical is seeking a Quality Control Inspector I responsible for inspecting, testing, and auditing raw materials and finished products. The role includes ensuring compliance with quality policies and regulations, driving continuous improvement, and interacting with various teams to maintain product quality.
Health CareMedical DeviceWholesale
Responsibilities
Inspect and release raw materials, components, sub-assemblies, and finished devices according to procedure
Drives continuous improvement activities with cross-functional team members
Generate non-conformances and escalate to the Material Review Board in a timely manner
Interacts with production areas, manufacturing and design engineering, marketing, quality, and management
Promotes a work environment of continuous improvement that supports CQ Medical's Quality Policy, Quality System, and the appropriate regulations
Assists with communicating business-related issues or opportunities for improvement to management
Accountable for compliance with applicable US and International regulations and directives including, but not limited to, Food & Drug Administration (FDA), Canadian and European Union regulations
Works in a team environment to achieve metrics
Interprets engineering drawings, schematic diagrams, sampling tables, or formulas and confers with management or engineering staff to determine quality and reliability standards
Selects products for tests at specified stages in production process, and tests products for variety of qualities such as dimensions, performance, mechanical, or chemical characteristics
Records test data, applying statistical quality control procedures using GMP documentation practices
Recommends modifications of existing quality or production standards to achieve optimum quality within limits of equipment capability
Quarantines all incoming material until testing is accepted
Quarantines all non-conforming material during any step of the manufacturing process until the Material Review Board dispositions the material
Purging of records as required
Maintains a neat and organized work area
Remains current on all required training
Conducts calibrations and works with 3rd party calibration providers to ensure inspection equipment meets specifications
Conducts transactions in the Quality Management System and/or ERP system to detail the disposition of incoming and in-process materials
Qualification
Required
Attention to detail is an expectation
Demonstration of commitment to patient safety and product quality by maintaining compliance with the Quality Policy and all other documented quality processes and procedures
Inspect and release raw materials, components, sub-assemblies, and finished devices according to procedure
Drives continuous improvement activities with cross-functional team members
Generate non-conformances and escalate to the Material Review Board in a timely manner
Interacts with production areas, manufacturing and design engineering, marketing, quality, and management
Promotes a work environment of continuous improvement that supports CQ Medical's Quality Policy, Quality System, and the appropriate regulations
Assists with communicating business-related issues or opportunities for improvement to management
Accountable for compliance with applicable US and International regulations and directives including, but not limited to, Food & Drug Administration (FDA), Canadian and European Union regulations
Works in a team environment to achieve metrics
Interprets engineering drawings, schematic diagrams, sampling tables, or formulas and confers with management or engineering staff to determine quality and reliability standards
Selects products for tests at specified stages in production process, and tests products for variety of qualities such as dimensions, performance, mechanical, or chemical characteristics
Records test data, applying statistical quality control procedures using GMP documentation practices
Recommends modifications of existing quality or production standards to achieve optimum quality within limits of equipment capability
Quarantines all incoming material until testing is accepted
Quarantines all non-conforming material during any step of the manufacturing process until the Material Review Board dispositions the material
Purging of records as required
Maintains a neat and organized work area
Remains current on all required training
Conducts calibrations and works with 3rd party calibration providers to ensure inspection equipment meets specifications
Conducts transactions in the Quality Management System and/or ERP system to detail the disposition of incoming and in-process materials
Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals
Ability to write routine reports and correspondence
Ability to speak effectively before groups of auditors or employees of our organization
Ability to interact effectively with individuals and teams
Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, percent, and interpret bar graphs
Decision-making ability
Ability to use testing equipment
Must be able to manage multiple tasks and perform with accuracy and a high attention to detail
Ability to identify priorities and function independently required
Ability to apply common sense understanding to carry out detailed but uninvolved written or oral instructions. Identify various discrepancies (product, process, documentation, etc.)
Analytical and problem-solving skills
Computer proficiency, including data entry. MS Office Suite (Word, PowerPoint, and Excel) experience required
50 lbs. of lifting required for this role
Hearing protection, safety glasses, safety shoes, and gloves are required for this role
Required exposure to biohazard
High school diploma or general education degree (GED)
Preferred
Medical device or manufacturing experience a plus
Preferred demonstration of leadership
Company
CQ Medical
CQ Medical focuses on radiotherapy positioning and healthcare innovations for improved patient care.
Founded in 1982
201-500 employees
Funding
Current Stage
Growth StageRecent News
Canada NewsWire
2025-12-02
2025-06-01
2025-04-04
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