Cadence, Inc.
Overview
Join to apply for the
Quality Assurance Lead
role at
Cadence, Inc. Cadence Inc. seeks an experienced
Quality Supervisor
to support our Cranston, Rhode Island Quality team. This is a salaried, exempt position and is on the first shift. Responsibilities
Overseeing Quality Control Processes and Inspection Activities: Establish and enforce quality standards, processes, and procedures across production and testing stages. Monitor day-to-day quality control activities to ensure product consistency and adherence to specifications. Team Supervision and Training Development: Manage a team of quality inspection employees, oversee their work, train team members on quality standards, testing methods, and safety protocols; conduct performance evaluations and facilitate team development and training opportunities; hold regular team meetings to communicate quality objectives and drive performance improvement. Inspecting and Testing Products: Supervise product inspections and quality tests to identify defects or deviations; use tools and technology to measure and verify product quality, ensuring specifications are met. Implementing Quality Improvement Plans: Identify areas for improvement in production processes to enhance product quality and efficiency; collaborate with other departments to implement process improvements aligned with quality goals. Developing and Updating QC Documentation: In conjunction with Quality Manager, update and maintain documentation related to quality standards, policies, and procedures; ensure documentation is clear, accurate, and available for team members. Ensuring Compliance with Regulations and Standards: Stay updated on relevant industry standards, laws, and regulations and ensure compliance; regularly review and adjust quality processes to adhere to regulatory requirements. Analyzing Data and Reporting: Analyze quality data, inspection results, and other metrics to identify trends and root causes of quality issues; compile reports on quality performance, nonconformance, and corrective actions, presenting findings to upper management. Continuous Improvement: Identify areas for improvement in the inspection process and collaborate with quality engineering, operations, and manufacturing engineering teams to implement corrective and preventive actions; participate in root cause analyses for quality issues and contribute to continuous improvement initiatives. Ensuring Safety and Compliance: Enforce safety protocols in the QC area to protect employees and maintain compliance with safety regulations; report safety hazards and work with safety personnel to resolve issues. Inventory and Equipment Management: Oversee maintenance and calibration of quality control equipment and testing tools; ensure the QC area has the necessary supplies and tools to perform inspections and tests effectively. Communication & Collaboration: Collaborate with cross-functional teams, including production, quality engineering, and manufacturing engineering, to ensure alignment on quality standards; serve as the point of contact for external audits or customer visits related to inspection activities. Qualifications
Minimum of 5 years experience in quality inspection within a regulated industry, preferably in medical device manufacturing. Minimum of 2 years of experience in a supervisory and/or leadership role, managing a team of individuals. Education: Technical degree in a related field preferred or equivalent experience. Knowledge, Skills & Abilities
Ability to effectively lead and manage a team of Quality Inspection employees, promoting collaboration, communication, and a positive work culture; delegate responsibilities and foster ownership and accountability. Strong leadership and team management skills; excellent attention to detail and problem-solving abilities; effective written and verbal communication; ability to work under pressure and meet deadlines. Proficiency in using Quality Management Software platforms; advanced data analysis tools (e.g., Microsoft Excel, Tableau, Power BI); statistical analysis tools; ERP systems (e.g., SAP, Oracle); database management; document management; email platforms; risk management software; project management tools; process mapping tools; CRM software; audit management software; LMS platforms; and other quality-related software. Ability to adapt to new software tools and technologies; strong planning and organizational skills. Certifications
ASQ Certified Quality Inspector (CQI) or Certified Quality Technician (CQT) preferred. Familiarity with Lean or Six Sigma methodologies for process improvement. Physical Demands
Must be able to function in both office and manufacturing environments. May require time on the production floor; standard computer use for extended periods; ability to move throughout the facility safely and interact with employees. Monday - Friday (8am - 4:30pm)
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Join to apply for the
Quality Assurance Lead
role at
Cadence, Inc. Cadence Inc. seeks an experienced
Quality Supervisor
to support our Cranston, Rhode Island Quality team. This is a salaried, exempt position and is on the first shift. Responsibilities
Overseeing Quality Control Processes and Inspection Activities: Establish and enforce quality standards, processes, and procedures across production and testing stages. Monitor day-to-day quality control activities to ensure product consistency and adherence to specifications. Team Supervision and Training Development: Manage a team of quality inspection employees, oversee their work, train team members on quality standards, testing methods, and safety protocols; conduct performance evaluations and facilitate team development and training opportunities; hold regular team meetings to communicate quality objectives and drive performance improvement. Inspecting and Testing Products: Supervise product inspections and quality tests to identify defects or deviations; use tools and technology to measure and verify product quality, ensuring specifications are met. Implementing Quality Improvement Plans: Identify areas for improvement in production processes to enhance product quality and efficiency; collaborate with other departments to implement process improvements aligned with quality goals. Developing and Updating QC Documentation: In conjunction with Quality Manager, update and maintain documentation related to quality standards, policies, and procedures; ensure documentation is clear, accurate, and available for team members. Ensuring Compliance with Regulations and Standards: Stay updated on relevant industry standards, laws, and regulations and ensure compliance; regularly review and adjust quality processes to adhere to regulatory requirements. Analyzing Data and Reporting: Analyze quality data, inspection results, and other metrics to identify trends and root causes of quality issues; compile reports on quality performance, nonconformance, and corrective actions, presenting findings to upper management. Continuous Improvement: Identify areas for improvement in the inspection process and collaborate with quality engineering, operations, and manufacturing engineering teams to implement corrective and preventive actions; participate in root cause analyses for quality issues and contribute to continuous improvement initiatives. Ensuring Safety and Compliance: Enforce safety protocols in the QC area to protect employees and maintain compliance with safety regulations; report safety hazards and work with safety personnel to resolve issues. Inventory and Equipment Management: Oversee maintenance and calibration of quality control equipment and testing tools; ensure the QC area has the necessary supplies and tools to perform inspections and tests effectively. Communication & Collaboration: Collaborate with cross-functional teams, including production, quality engineering, and manufacturing engineering, to ensure alignment on quality standards; serve as the point of contact for external audits or customer visits related to inspection activities. Qualifications
Minimum of 5 years experience in quality inspection within a regulated industry, preferably in medical device manufacturing. Minimum of 2 years of experience in a supervisory and/or leadership role, managing a team of individuals. Education: Technical degree in a related field preferred or equivalent experience. Knowledge, Skills & Abilities
Ability to effectively lead and manage a team of Quality Inspection employees, promoting collaboration, communication, and a positive work culture; delegate responsibilities and foster ownership and accountability. Strong leadership and team management skills; excellent attention to detail and problem-solving abilities; effective written and verbal communication; ability to work under pressure and meet deadlines. Proficiency in using Quality Management Software platforms; advanced data analysis tools (e.g., Microsoft Excel, Tableau, Power BI); statistical analysis tools; ERP systems (e.g., SAP, Oracle); database management; document management; email platforms; risk management software; project management tools; process mapping tools; CRM software; audit management software; LMS platforms; and other quality-related software. Ability to adapt to new software tools and technologies; strong planning and organizational skills. Certifications
ASQ Certified Quality Inspector (CQI) or Certified Quality Technician (CQT) preferred. Familiarity with Lean or Six Sigma methodologies for process improvement. Physical Demands
Must be able to function in both office and manufacturing environments. May require time on the production floor; standard computer use for extended periods; ability to move throughout the facility safely and interact with employees. Monday - Friday (8am - 4:30pm)
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