Quality Manager
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Before you apply
Salary$100k – $130k
LocationSan Diego, California, United States
Work modeon-site
Typefull-time
SenioritySenior
Experience10+ yrs
DepartmentSan Diego
Company size1,001–5,000 people
PostedOct 23, 2024 · 2y ago
Verified live2d ago
May no longer be actively hiring
Posted by the company on Oct 23, 202495% of this company's open roles have been listed for 90+ days
At a glanceSummarised by Seekless from the posting.
Minimum Bachelor's degree in Science or related field
Thorough knowledge of US FDA 21 CFR 820 Quality System Regulation and ISO 13485:2016 standards
Strong understanding of quality management principles and practices in the medical device industry
Excellent communication and interpersonal skills
Ability to work collaboratively in a team environment
Demonstrated problem-solving and analytical skills
Attention to detail and strong organizational skills
Minimum 10 Years experience in Medical devices, Quality Management, Regulatory compliance and ISO standards
ISO 13485:2016 lead auditor certification preferred
We are an equal-opportunity employer and celebrate diversity...We do not discriminate...
Skills
Statistical analysis
Benefits
Medical insurance
Retirement plan
Paid time off
Training and development
About the role
We are looking for an experienced Quality Manager to ensure that our products and services meet all necessary requirements before they reach the consumer. The Quality Manager, or Quality Assurance Manager, will inspect the final product to make sure it has been built with compliance to legal standards and meets customer expectations. A great quality manager is thorough and observant with an eye for detail. They must fully understand the requirements for the product or service and have a sense of responsibility towards our potential and existing customers as well as the competition. The goal is to help preserve our reputation by ensuring that our products and services are capable to drive sustainable growth.
Position: Quality Manager
Location: San Diego(Onsite)
Salary: $100,000- $130,000
Responsibilities
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Understand customer needs and requirements to develop effective quality control processes
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Devise and review specifications for products or processes
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Set requirements for raw material or intermediate products for suppliers and monitor their compliance
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Ensure adherence to health and safety guidelines as well as legal obligations
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Supervise inspectors, technicians and other staff and provide guidance and feedback
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Oversee all product development procedures to identify deviations from quality standards
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Inspect final output and compare properties to requirements
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Approve the right products or reject defectives
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Keep accurate documentation and perform statistical analysis
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Solicit feedback from customers to assess whether their requirements are met
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Submit detailed reports to appropriate executives
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Implement, manage, and improve the company’s quality management system, with a primary focus on IVD products and equipment.
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Conduct internal audits, compile audit reports, perform problem analysis, propose improvement initiatives, and monitor the implementation of corrective and preventive actions (CAPA).
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Lead and participate in internal audits and management reviews of the company’s quality system as a key member of the quality department.
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Manage the documentation of the company’s quality management system, ensuring compliance with relevant standards and regulations.
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Oversee the quality management system for IVD equipment, ensuring compliance with applicable regulations and standards.
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Perform statistical analysis of IVD equipment quality data, prepare reports, and develop corrective and preventive measures as needed.
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Update company documents in accordance with new or revised quality standards, laws, and regulations.
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Establish collaborative relationships with key opinion leaders and certification bodies to ensure alignment with industry best practices and regulatory requirements.
Requirements
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Minimum Bachelor’s degree in Science or related field.
•
ISO 13485:2016 lead auditor certification preferred.
•
Thorough knowledge of US FDA 21 CFR 820 Quality System Regulation and ISO 13485:2016 standards.
•
Strong understanding of quality management principles and practices in the medical device industry.
•
Excellent communication and interpersonal skills.
•
Ability to work collaboratively in a team environment.
•
Demonstrated problem-solving and analytical skills.
•
Attention to detail and strong organizational skills.
•
Minimum 10 Years experience in Medical devices, Quality Management , Regulatory compliance and ISO standards
Benefits
•
Medical Insurance Plan
•
Retirement Plan
•
Paid Time Off
•
Training & Development
Legal
We are an equal-opportunity employer and celebrate diversity, recognizing that diversity of thought and background builds stronger teams. We approach diversity and inclusion seriously and thoughtfully. We do not discriminate on the basis of race, religion, color, ancestry, national origin, caste, sex, sexual orientation, gender, gender identity or expression, age, disability, medical condition, pregnancy, genetic makeup, marital status, or military service