What are the responsibilities and job description for the Product Quality Specialist position at Cypress HCM?
Job Overview:
Cypress HCM is a leading manufacturer of health, beauty, and cosmetic products. We are currently seeking an experienced Quality Engineer to join our team in Eagan, Minnesota.
About the Role:
This is a unique opportunity for a highly motivated individual to drive quality improvements across our manufacturing operations. As a Quality Engineer, you will be responsible for identifying and analyzing quality problems, developing effective solutions, and implementing process improvements to ensure compliance with industry standards and regulatory requirements.
Main Responsibilities:
* Lead quality-related problem-solving and root cause analysis in manufacturing to prevent recurrences
* Participate in the investigation of technical issues, status of testing, and the establishment of procedures and CAPA to ensure product quality and regulatory compliance
* Operate independently, representing the quality organization in major meetings to resolve key issues and plan work
* Coordinate cross-functional teams to address Non-Conformance issues to reduce scrap and improve First Pass Yield (FPY)
Requirements:
* Bachelor's degree in Engineering (Master's degree preferred)
* 3-5 years of experience in cosmetics, medical device, or pharmaceuticals with a Bachelor's degree, or 1-2 years with a Master's degree
* Strong knowledge of quality systems (ISO 9001, GMP, FDA regulations), personal care industry standards, and regulatory compliance
Preferred Qualifications:
* Six Sigma Green or Black Belt certification
* Certified Quality Engineer (CQE) certification
* ISO 9001 Lead Auditor Certification
Contact Information:
Please submit your resume and cover letter to apply for this exciting opportunity.
Cypress HCM is a leading manufacturer of health, beauty, and cosmetic products. We are currently seeking an experienced Quality Engineer to join our team in Eagan, Minnesota.
About the Role:
This is a unique opportunity for a highly motivated individual to drive quality improvements across our manufacturing operations. As a Quality Engineer, you will be responsible for identifying and analyzing quality problems, developing effective solutions, and implementing process improvements to ensure compliance with industry standards and regulatory requirements.
Main Responsibilities:
* Lead quality-related problem-solving and root cause analysis in manufacturing to prevent recurrences
* Participate in the investigation of technical issues, status of testing, and the establishment of procedures and CAPA to ensure product quality and regulatory compliance
* Operate independently, representing the quality organization in major meetings to resolve key issues and plan work
* Coordinate cross-functional teams to address Non-Conformance issues to reduce scrap and improve First Pass Yield (FPY)
Requirements:
* Bachelor's degree in Engineering (Master's degree preferred)
* 3-5 years of experience in cosmetics, medical device, or pharmaceuticals with a Bachelor's degree, or 1-2 years with a Master's degree
* Strong knowledge of quality systems (ISO 9001, GMP, FDA regulations), personal care industry standards, and regulatory compliance
Preferred Qualifications:
* Six Sigma Green or Black Belt certification
* Certified Quality Engineer (CQE) certification
* ISO 9001 Lead Auditor Certification
Contact Information:
Please submit your resume and cover letter to apply for this exciting opportunity.
