Quality Lead Salary at Imerit BETA

Job Title: Senior Product Quality Engineer Department: Quality Assurance Location: San Jose, California Type: Full-Time Job Description: Directly interface with automotive customer quality engineers to collaborate on product quality topics Directly interface with internal teams to address product development quality Lead 8D investigations for quality issues and work to deploy systemic corrective actions Create customer facing 8D reports Assist Sales team on customer quality matters Support customer PPAP and documentation requests Requirements: BSEE degree Minimum of 8 years of experience in engineering role (Quality Engineering, Product Engineering, Test Engineering, Applications Engineering) supporting or developing automotive products or processes. Experience with AEC-Q100 product qualifications Direct Experience managing 8D investigations and creating 8D reports Enjoys working in cross-functional team environment Enjoys problem solving Preferred: Failure Analysis lab experience APQP

This full-time position offers flexible work hours and ample opportunities for advancement into management roles. You will work remotely to serve clients and offer valuable advice and protection to individuals and their families. What We Offer: • Remote, work from home career. • Average first-year earnings of $69K commission + bonuses. • Life-long residual income through renewals. • Unionized position with stock options. • Excellent benefits package - medical, dental, and prescription coverage. • Exceptional training with experienced managers. • High-quality leads provided: no calling family or friends. • Flexible hours: this is a fulltime career, but you can choose when you work. • Opportunities for advancement and recognition as we promote from within. • Dynamic Team Environment: Our virtual workplace thrives on a vibrant team atmosphere. While this position is remote, you will have lots of support. Qualities We Value: • Willingness to learn and be coached as we provide comprehensive

Manager/Senior Manager Clinical Quality Assurance We are seeking a skilled Clinical Quality Professinal to support study team compliance with national and international regulatory standards and guidelines for cell therapy products. This role offers the opportunity to contribute to a growing biotech focused on innovative therapies for oncology and autoimmune diseases. Key Responsibilities: Act as a Clinical Quality lead by ensuring study teams adhere to GCP and regulatory requirements. Develop and execute audit plans and strategies for ongoing clinical trials. Perform initial and ongoing audits of clinical vendors. Coordinate, plan, and conduct internal system audits and external site/vendor audits in accordance with GCP guidelines. Report audit findings to management, provide recommendations, and verify corrective actions. Support the development and maintenance of clinical SOPs, work instructions, forms, and templates. Develop and deliver GCP and inspection readiness training for staf

Manager/Senior Manager Clinical Quality Assurance We are seeking a skilled Clinical Quality Professinal to support study team compliance with national and international regulatory standards and guidelines for cell therapy products. This role offers the opportunity to contribute to a growing biotech focused on innovative therapies for oncology and autoimmune diseases. Key Responsibilities: Act as a Clinical Quality lead by ensuring study teams adhere to GCP and regulatory requirements. Develop and execute audit plans and strategies for ongoing clinical trials. Perform initial and ongoing audits of clinical vendors. Coordinate, plan, and conduct internal system audits and external site/vendor audits in accordance with GCP guidelines. Report audit findings to management, provide recommendations, and verify corrective actions. Support the development and maintenance of clinical SOPs, work instructions, forms, and templates. Develop and deliver GCP and inspection readiness training for staf

Manager/Senior Manager Clinical Quality Assurance We are seeking a skilled Clinical Quality Professinal to support study team compliance with national and international regulatory standards and guidelines for cell therapy products. This role offers the opportunity to contribute to a growing biotech focused on innovative therapies for oncology and autoimmune diseases. Key Responsibilities: Act as a Clinical Quality lead by ensuring study teams adhere to GCP and regulatory requirements. Develop and execute audit plans and strategies for ongoing clinical trials. Perform initial and ongoing audits of clinical vendors. Coordinate, plan, and conduct internal system audits and external site/vendor audits in accordance with GCP guidelines. Report audit findings to management, provide recommendations, and verify corrective actions. Support the development and maintenance of clinical SOPs, work instructions, forms, and templates. Develop and deliver GCP and inspection readiness training for staf

Manager/Senior Manager Clinical Quality Assurance We are seeking a skilled Clinical Quality Professinal to support study team compliance with national and international regulatory standards and guidelines for cell therapy products. This role offers the opportunity to contribute to a growing biotech focused on innovative therapies for oncology and autoimmune diseases. Key Responsibilities: Act as a Clinical Quality lead by ensuring study teams adhere to GCP and regulatory requirements. Develop and execute audit plans and strategies for ongoing clinical trials. Perform initial and ongoing audits of clinical vendors. Coordinate, plan, and conduct internal system audits and external site/vendor audits in accordance with GCP guidelines. Report audit findings to management, provide recommendations, and verify corrective actions. Support the development and maintenance of clinical SOPs, work instructions, forms, and templates. Develop and deliver GCP and inspection readiness training for staf

Manager/Senior Manager Clinical Quality Assurance We are seeking a skilled Clinical Quality Professinal to support study team compliance with national and international regulatory standards and guidelines for cell therapy products. This role offers the opportunity to contribute to a growing biotech focused on innovative therapies for oncology and autoimmune diseases. Key Responsibilities: Act as a Clinical Quality lead by ensuring study teams adhere to GCP and regulatory requirements. Develop and execute audit plans and strategies for ongoing clinical trials. Perform initial and ongoing audits of clinical vendors. Coordinate, plan, and conduct internal system audits and external site/vendor audits in accordance with GCP guidelines. Report audit findings to management, provide recommendations, and verify corrective actions. Support the development and maintenance of clinical SOPs, work instructions, forms, and templates. Develop and deliver GCP and inspection readiness training for staf

Manager/Senior Manager Clinical Quality Assurance We are seeking a skilled Clinical Quality Professinal to support study team compliance with national and international regulatory standards and guidelines for cell therapy products. This role offers the opportunity to contribute to a growing biotech focused on innovative therapies for oncology and autoimmune diseases. Key Responsibilities: Act as a Clinical Quality lead by ensuring study teams adhere to GCP and regulatory requirements. Develop and execute audit plans and strategies for ongoing clinical trials. Perform initial and ongoing audits of clinical vendors. Coordinate, plan, and conduct internal system audits and external site/vendor audits in accordance with GCP guidelines. Report audit findings to management, provide recommendations, and verify corrective actions. Support the development and maintenance of clinical SOPs, work instructions, forms, and templates. Develop and deliver GCP and inspection readiness training for staf