What are the responsibilities and job description for the Quality Control Expert - Medical Devices position at Cypress HCM?
Job Summary:
Cypress HCM is seeking a dedicated Quality Engineer to join our team in Eagan, Minnesota. In this role, you will be responsible for driving quality improvements across our manufacturing operations, ensuring compliance with industry standards and regulatory requirements. You will work closely with cross-functional teams to identify and solve quality-related problems, develop effective solutions, and implement process improvements.
Main Responsibilities:
* Analyze quality data to identify trends and areas for improvement
* Develop and implement quality control systems and processes to ensure compliance with industry standards and regulatory requirements
* Participate in the investigation of technical issues, status of testing, and the establishment of procedures and CAPA to ensure product quality and regulatory compliance
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 seeking a dedicated Quality Engineer to join our team in Eagan, Minnesota. In this role, you will be responsible for driving quality improvements across our manufacturing operations, ensuring compliance with industry standards and regulatory requirements. You will work closely with cross-functional teams to identify and solve quality-related problems, develop effective solutions, and implement process improvements.
Main Responsibilities:
* Analyze quality data to identify trends and areas for improvement
* Develop and implement quality control systems and processes to ensure compliance with industry standards and regulatory requirements
* Participate in the investigation of technical issues, status of testing, and the establishment of procedures and CAPA to ensure product quality and regulatory compliance
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.
