Quality Engineer

Job Summary

We are seeking a highly motivated and experienced Quality Engineer to join our team. As a Quality Engineer, you will be responsible for ensuring the quality of our products and processes, identifying and implementing improvements to ensure compliance with regulatory requirements and industry standards. This is a full-time position that will report to the Quality Manager.

Responsibilities

• Develop and implement quality plans, procedures, and protocols to ensure compliance with regulatory requirements and industry standards.

• Conduct quality audits and inspections to identify areas for improvement and implement corrective actions.

• Investigate customer complaints and product failures to identify root causes and implement corrective actions.

• Collaborate with cross-functional teams to develop and implement quality improvement initiatives.

• Conduct root cause analysis and implement corrective actions to prevent recurrence of defects.

• Develop and maintain quality metrics and reports to track performance and identify areas for improvement.

• Participate in continuous improvement initiatives to improve processes and reduce defects.

• Collaborate with suppliers to ensure compliance with quality standards and regulations.

• Develop and maintain documentation of quality processes, procedures, and protocols.

Requirements

• Bachelor's degree in Engineering, Quality Assurance, or a related field.

• 3+ years of experience in a quality engineering or related field.

• Strong knowledge of quality principles, regulations, and industry standards (e.g. ISO 9001, FDA GMP, etc.).

• Excellent analytical and problem-solving skills.

• Strong communication and interpersonal skills.

• Ability to work effectively in a team environment.

• Strong attention to detail and organizational skills.

• Ability to prioritize tasks and manage multiple projects simultaneously.

• Familiarity with statistical process control (SPC) and statistical analysis (SAS) is a plus.

Preferred Qualifications

• Master's degree in Engineering or a related field.

• ASQ (American Society for Quality) certification (e.g. CQE, CQA).

• Experience in the medical device or pharmaceutical industry.

• Knowledge of regulatory requirements (e.g. FDA, EU MDR).

• Experience with quality management software (e.g. TrackWise, Lighthouse).

What We Offer

• Competitive salary and benefits package.

• Opportunities for professional growth and development.

• Collaborative and dynamic work environment.

• Recognition and rewards for outstanding performance.

• Flexible work arrangements (e.g. telecommuting options).

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

• Hiring diverse talent

• Maintaining an inclusive environment through persistent self-reflection

• Building a culture of care, engagement, and recognition with clear outcomes

• Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email ~~~ (~~~) for other accommodation options.