Quality Engineer - Manufacturing

We are seeking a Permanent Quality Engineer to join our dynamic team in the Medical Device industry. The candidate must have a minimum of 5 years of experience in the field and be proficient in quality engineering, medical device regulations, CAPA, audit, quality management systems, and root cause analysis. As a Quality Engineer, you will be responsible for ensuring the highest level of quality in our products and processes.

Excellent Compensation ** Up To $130,000 **

• Competitive wages paid weekly for full and part time opportunities
• Generous paid time off program - work your way up to over 5 weeks of paid time off a year!
• Medical, dental, and vision benefits after a short waiting period
• Company paid life insurance
• 401k plus company match
• Performance bonuses
• Growth opportunities

Responsibilities:

• Develop and implement quality control procedures and processes to ensure compliance with regulatory requirements and customer satisfaction
• Conduct audits and assessments to identify areas for improvement and implement corrective and preventive actions (CAPA)
• Investigate and analyze quality-related issues, perform root cause analysis, and develop solutions to prevent recurrence
• Collaborate with cross-functional teams to ensure effective communication and implementation of quality initiatives
• Monitor and analyze quality metrics to identify trends and opportunities for improvement
• Maintain and improve the quality management system to ensure compliance with regulatory standards and industry best practices
• Provide training and guidance to employees on quality-related topics
• Participate in the development and review of product specifications, design documentation, and manufacturing processes to ensure quality requirements are met

Qualifications:

• Bachelor's degree in engineering, science, or related field
• Minimum of 5 years of experience in quality engineering in the medical device industry
• Strong knowledge of quality management systems, regulatory requirements, and industry standards (ISO 13485, FDA regulations, etc.)
• Experience with CAPA, audit, and root cause analysis
• Excellent problem-solving and analytical skills
• Strong communication and interpersonal skills
• Ability to work independently and collaboratively in a team environment
• Detail-oriented and organized with the ability to manage multiple tasks simultaneously

If you are a results-driven individual with a passion for quality and a desire to make a difference, we encourage you to apply for this exciting opportunity as a Permanent Quality Engineer in the manufacturing industry.