11/14/2025
Dynamic is looking for a Quality Engineer.
The Quality Engineer is responsible for supporting, maintaining, and improving the Quality Management System (QMS) in compliance with ISO standards and regulatory requirements. This role focuses on process validation and creation, quality control, and problem-solving to ensure products and processes meet customer and regulatory expectations. The Quality Engineer participates in audits, drives corrective and preventive actions, supports safety initiatives, and collaborates with cross-functional teams to promote a culture of quality, safety, and continuous improvement.
The individual in this position must be able to successfully perform the job duties listed below.
Responsibilities:
• Support and maintain the company’s Quality Management System (QMS) in accordance with ISO 9001 and other applicable standards.
• Participate in internal and external audits, including customer and regulatory audits.
• Assist in developing and updating quality policies, procedures, and documentation.
• Monitor and report on key quality metrics; drive and track corrective/preventive actions (CAPA).
• Ensure compliance with customer-specific requirements and industry regulations.
• Train and support employees on quality standards, procedures, and best practices.
• Collaborate with engineering, production, and supply chain teams to resolve quality issues.
• Conduct root cause analysis and support continuous improvement initiatives.
• Maintain document control and change management systems.
• Actively support and participate in safety initiatives, ensuring that quality processes align with company safety policies and regulatory requirements.
• Work with the safety team to identify and mitigate risks and promote a safe working environment through quality and safety audits.
Related Experience:
Experience in quality engineering, quality systems management, or manufacturing environments. Familiarity with ISO 9001, GMP, or other regulatory frameworks is preferred.
Certifications/Tech expertise:
• Certified Quality Auditor (CQA), Certified Quality Engineer (CQE), or similar preferred
• Proficiency in quality tools such as FMEA, SPC, CAPA, and root cause analysis
• Experience with Microsoft Office and document control systems
PREFERRED QUALIFICATIONS:
• Knowledge of ISO 9001, GMP, and other quality standards
• Knowledge of ISO 13485, medical device or regulated industries is a plus
• Familiar with value stream mapping and other Lean management tools such as 5S and root cause analysis.
• Strong leadership and communication skills
• Detail-oriented with strong analytical and problem-solving abilities
Apply via our website:
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