Manager - Supplier Quality Assurance Devices (f/m/x)
at ZEISS Group
Oberkochen, Baden-Württemberg, Germany -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 30 Jul, 2024 | Not Specified | 05 May, 2024 | N/A | Good communication skills | No | No |
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Contract to Hire – Corp 2 Corp |
Description:
Your Role
- responsible to advise all quality aspects regarding Supplier Quality Assurance to ensure safety, effectiveness, reliability, and quality capability of purchased material from suppliers
- implement best practices for managing supplier non-conformities and incoming inspection processes while ensuring precise assessment of incoming materials and components meet regulatory standards
- define and monitor key performance indicators (KPIs) to measure supplier performance, incoming inspection effectiveness, and complaint management with a strong focus on regulatory compliance
- establish and maintain strong partnerships with suppliers, fostering quality improvements and adherence to the medical device industry standards and regulations
- collaborate closely with cross-functional teams, including quality management, production, procurement, and engineering, to drive quality initiatives and sustainably resolve supplier-related issues
- drive continuous improvement efforts aimed at enhancing quality, reducing defects, and optimizing costs within the medical device supply chain
- stay well-informed about evolving medical device industry trends and regulations pertaining to supplier quality and inspection
- drive digitalization and process improvement initiatives to enhance supplier quality assurance to its next level
- maintain constant contact with the global Supplier Quality teams to achieve continuous development
Your Profile
- Bachelor or Master of Science/ Engineering or comparable, required
- minimum 5 years of experience in supplier quality management or related roles in quality
- extensive knowledge of quality assurance & quality management systems, ISO 13485, ISO 9001, AQL, APQP, MSA, 8D, CAPA, MDR, FDA regulations, and other relevant medical device industry standards
- expert in interpretation of technical drawing (GD&T) and AQL sampling plan table
- strong problem-solving skills and the ability to manage multiple priorities simultaneously
- excellent interpersonal and leadership skills, ability to effectively manage internal/external cross-functional teams with the understanding of cross-functional tensions
- analytical mindset with the ability to identify trends and implement data-driven decisions
- willingness to travel domestically and internationally as required
- fluent in German and English, French would be an advantage
Your ZEISS Recruiting Team:
Marina Lö
Responsibilities:
- responsible to advise all quality aspects regarding Supplier Quality Assurance to ensure safety, effectiveness, reliability, and quality capability of purchased material from suppliers
- implement best practices for managing supplier non-conformities and incoming inspection processes while ensuring precise assessment of incoming materials and components meet regulatory standards
- define and monitor key performance indicators (KPIs) to measure supplier performance, incoming inspection effectiveness, and complaint management with a strong focus on regulatory compliance
- establish and maintain strong partnerships with suppliers, fostering quality improvements and adherence to the medical device industry standards and regulations
- collaborate closely with cross-functional teams, including quality management, production, procurement, and engineering, to drive quality initiatives and sustainably resolve supplier-related issues
- drive continuous improvement efforts aimed at enhancing quality, reducing defects, and optimizing costs within the medical device supply chain
- stay well-informed about evolving medical device industry trends and regulations pertaining to supplier quality and inspection
- drive digitalization and process improvement initiatives to enhance supplier quality assurance to its next level
- maintain constant contact with the global Supplier Quality teams to achieve continuous developmen
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Production / Maintenance / Quality
Software Testing, Clinical Pharmacy
Graduate
Proficient
1
Oberkochen, Germany