QMS Manager
- Compensation
- Not disclosed
- Location
- Not listed
- Work setup
- Not specified
- Seniority
- Not specified
- Employment
- Not specified
- Experience
- 5+ years
- Category
- Not specified
- Posted
Skills
Must have
- Bachelor of Science degree required, BS in Electrical, Industrial, Mechanical Engineering, Quality Management, or related field.
- 5+ years of experience in Quality Management within Advanced Manufacturing, Bioscience, Semiconductor, Aerospace, or Defense Industry Environment
- Strong knowledge of quality standards and regulations (ISO 9001, ISO 13485, ISO 14971, IATF 16949, FDA 21 CFR 820)
Nice to have
- ASQ certified Quality Manager, ISO Lead Auditor Certification, Technical Writing
- Understanding and familiarity with design history files, change management, manufacturing process control, material review boards, failure analysis, corrective/preventive actions, and verification tes
- Experience in NPI (New Product Introductions) process management and product quality planning
- Formal training in statistical techniques in a manufacturing environment with Six Sigma training and certification
- Knowledge and experience with continuous improvement techniques such as Lean Enterprise, Six Sigma, Kaizen, SPC, etc.
- Experience in Supplier Quality Management
- Excellent verbal and written skills, including proficiency in MS Office Suite of applications
Full description
ENABLE your future through light.
Excelitas is a global technology leader with more than 7,500 employees, focused on delivering market-driven solutions to fulfill the illumination, optical, detection and imaging needs of OEMs and end-users across the biomedical, semiconductor, industrial, consumer products, scientific, security, defense and aerospace sectors.
ENGAGE with us today and make your contribution to the future! Join the team that leading technology companies turn to for cutting-edge photonic innovation. At Excelitas Technologies you are how we EXCEL.
We are presently seeking a Quality Management System Manager that be responsible for continous improvement and maintenance of the site QMS and in the support of manufacutring process improvements.
Main responsibilities:
- Oversee all Quality Management System functions, including Document Control, Internal QMS Audits, Customer & Supplier Audits, Returned Material Authorizations, and Customer Complaints.
- Improve and optimize the Quality Management System (QMS) to ensure effectiveness and efficiency while ensuring the standardization of procedures within Excelitas globally
- Support quality improvement initiatives at the site to address the cost of poor-quality contributors
- Cultivate a culture of continuous improvement and operational excellence within the organization
- Provide cross-functional team leadership to drive quality and yield improvement initiatives
- Ensure that all manufacturing processes and finished products meet internal specifications, customer requirements, and regulatory compliance standards
- Plan, coordinate, and actively engage in new product introductions (NPI), product qualifications, design verifications, and risk assessments, which encompass process failure mode and effects analysis.
- Ensure adherence to ISO standards such as ISO 9001, ISO 13485, ISO 14971, and FDA 21 CFR 820 according to site accreditation requirements
- Address and resolve customer complaints through effective corrective and preventative actions
- Utilize statistical tools and root cause analysis methods such as SPC, Pareto Diagrams, Affinity Diagrams, Fault-Tree Analysis, Design of Experiments, Fish-Bone Analysis, to drive quality improvements, including training and guidance to site employees
- Assist in the maintenance and training of the site on ISO standards and regulations according to site accreditations
- Support and coordinate site Root Cause Investigations and Corrective and Preventative Actions (CAPA), including Supplier Corrective Actions (SCARS)