Quality Engineer at Jobot
Rockville, MD 20850
About the Job
Well established manufacturing company is seeking a skilled Quality Engineer to join their growing team!
This Jobot Job is hosted by: Ryan Anderson
Are you a fit? Easy Apply now by clicking the "Quick Apply" button
and sending us your resume.
Salary: $110,000 - $125,000 per year
A bit about us:
As a Permanent Quality Engineer in the dynamic Manufacturing industry, you will have the opportunity to work in a fast-paced, innovative environment where your contributions will have a direct impact. This position is an integral part of our team, responsible for ensuring the quality of our products and services. You will be involved in all aspects of quality management, from design and development to production and customer support. With a focus on continuous improvement, you will utilize your skills in FTA, FMEA, 8D, A3, Six Sigma, SPC, data analysis, production quality control, and quality assurance to drive our quality objectives.
Why join us?
Competitive compensation, annual bonus, and benefits package! Relocation assistance available! 401k w employer match!!
Job Details
Job Details:
Our organization is a leading player in the Med Device Manufacturing industry, and we are currently seeking a highly skilled and motivated Permanent Quality Engineer to join our dynamic team. The successful applicant will be responsible for maintaining and improving our quality systems, ensuring compliance with industry and company standards, and playing a key role in the development of new products. This position requires a minimum of 5 years of experience in a similar role, preferably within the Medical Device Manufacturing industry.
Responsibilities:
1. Lead and execute quality improvement projects using tools such as FTA, FMEA, 8D, A3, Six Sigma, and SPC.
2. Conduct data analysis to identify areas for improvement in production quality control and implement necessary changes.
3. Ensure all quality assurance processes are in compliance with QSR, ISO 9001, and other relevant standards.
4. Play a key role in new product development, ensuring that all products meet the highest quality standards.
5. Implement and manage CAPA processes, identifying and addressing any non-conformities.
6. Work closely with the production team to ensure the quality of products, identifying and addressing any potential issues.
7. Maintain and improve quality systems for medical devices, ensuring compliance with all relevant regulations and standards.
8. Prepare and present quality reports to management, providing recommendations for improvement where necessary.
Qualifications:
1. Bachelor's or Master's degree in Engineering/Scientific/Technical or a related field.
2. A minimum of 4 years of experience as a Quality Engineer within the Medical Device, IV Diagnostics, Pharma, or related industries is a must.
3. Proficiency in FTA, FMEA, 8D, A3, Six Sigma, SPC, and other quality improvement tools.
4. Strong data analysis skills, with the ability to identify trends and make data-driven decisions.
5. Experience with production quality control and quality assurance processes.
6. Experience with new product development, with a strong focus on quality.
7. Knowledge of CAPA processes and experience implementing and managing these processes.
8. Knowledge of medical devices and the relevant quality systems and regulations.
9. Familiarity with QSR, ISO 9001, and other relevant standards.
10. Certifications such as ASQ, CQE, CRE, CQA, or equivalent are highly desirable.
11. Knowledge of TQM and experience implementing and managing quality systems.
12. Excellent problem-solving skills, with the ability to think critically and make sound decisions.
13. Strong communication skills, with the ability to effectively present information and influence others.
14. Ability to work in a fast-paced environment, managing multiple priorities simultaneously.
Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button.
This Jobot Job is hosted by: Ryan Anderson
Are you a fit? Easy Apply now by clicking the "Quick Apply" button
and sending us your resume.
Salary: $110,000 - $125,000 per year
A bit about us:
As a Permanent Quality Engineer in the dynamic Manufacturing industry, you will have the opportunity to work in a fast-paced, innovative environment where your contributions will have a direct impact. This position is an integral part of our team, responsible for ensuring the quality of our products and services. You will be involved in all aspects of quality management, from design and development to production and customer support. With a focus on continuous improvement, you will utilize your skills in FTA, FMEA, 8D, A3, Six Sigma, SPC, data analysis, production quality control, and quality assurance to drive our quality objectives.
Why join us?
Competitive compensation, annual bonus, and benefits package! Relocation assistance available! 401k w employer match!!
Job Details
Job Details:
Our organization is a leading player in the Med Device Manufacturing industry, and we are currently seeking a highly skilled and motivated Permanent Quality Engineer to join our dynamic team. The successful applicant will be responsible for maintaining and improving our quality systems, ensuring compliance with industry and company standards, and playing a key role in the development of new products. This position requires a minimum of 5 years of experience in a similar role, preferably within the Medical Device Manufacturing industry.
Responsibilities:
1. Lead and execute quality improvement projects using tools such as FTA, FMEA, 8D, A3, Six Sigma, and SPC.
2. Conduct data analysis to identify areas for improvement in production quality control and implement necessary changes.
3. Ensure all quality assurance processes are in compliance with QSR, ISO 9001, and other relevant standards.
4. Play a key role in new product development, ensuring that all products meet the highest quality standards.
5. Implement and manage CAPA processes, identifying and addressing any non-conformities.
6. Work closely with the production team to ensure the quality of products, identifying and addressing any potential issues.
7. Maintain and improve quality systems for medical devices, ensuring compliance with all relevant regulations and standards.
8. Prepare and present quality reports to management, providing recommendations for improvement where necessary.
Qualifications:
1. Bachelor's or Master's degree in Engineering/Scientific/Technical or a related field.
2. A minimum of 4 years of experience as a Quality Engineer within the Medical Device, IV Diagnostics, Pharma, or related industries is a must.
3. Proficiency in FTA, FMEA, 8D, A3, Six Sigma, SPC, and other quality improvement tools.
4. Strong data analysis skills, with the ability to identify trends and make data-driven decisions.
5. Experience with production quality control and quality assurance processes.
6. Experience with new product development, with a strong focus on quality.
7. Knowledge of CAPA processes and experience implementing and managing these processes.
8. Knowledge of medical devices and the relevant quality systems and regulations.
9. Familiarity with QSR, ISO 9001, and other relevant standards.
10. Certifications such as ASQ, CQE, CRE, CQA, or equivalent are highly desirable.
11. Knowledge of TQM and experience implementing and managing quality systems.
12. Excellent problem-solving skills, with the ability to think critically and make sound decisions.
13. Strong communication skills, with the ability to effectively present information and influence others.
14. Ability to work in a fast-paced environment, managing multiple priorities simultaneously.
Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button.
Salary
110,000 - 125,000 /year