MD
Manufacturing Quality Engineer
Macpower Digital Assets Edge Private Limited
πΊπΈ United States
Remote
Manager or above
5 days ago
$45 β $48 / hour
- Regulatory Compliance
- Green Belt
5 days ago
Not enough detail in this posting to match
Key Responsibilities:
- Design, implement, and maintain quality assurance protocols and methods for processing materials into partially finished or finished products for the supply chain.
- Plan, implement, and manage compliance of in-house and outsourced manufacturing processes with internal and external quality and regulatory standards for global distribution.
- Review inspection methods, testing procedures, and evaluation techniques to ensure precision and accuracy in production processes, equipment, components, and finished products.
- Analyze production reports and data trends to recommend updates or changes to quality standards and procedures.
- Ensure compliance with internal and external specifications and standards such as ISO 13485, MP, and MDSAP.
- Lead and facilitate investigations with cross-functional teams to identify root causes and implement corrective actions for product and component issues within the supply chain.
- Provide expertise in specialized quality assurance areas, requiring knowledge of key principles and concepts.
Additional Responsibilities:Depending on experience level, responsibilities may include:
- Performing routine quality assurance tasks (early career).
- Contributing to projects and process improvements (mid-career).
- Providing specialist guidance and expertise in primary focus areas.
- Leveraging professional experience to drive strategy and business results.
- Build and maintain productive internal/external working relationships.
- Occasionally lead project teams and provide training for junior staff.
Basic Qualifications and Experience:
- Bachelor's degree in a relevant field.
- Minimum 2 years of experience in manufacturing quality assurance.
- Experience applying company policies and procedures to resolve quality-related issues.
- Strong working knowledge of ISO 13485 and regulatory compliance for medical devices.
Must-Have Requirements:
- Bachelor's degree.
- Minimum 2 years of related experience.
- Strong knowledge of ISO 13485.
- Ability to apply professional expertise to resolve quality issues.
Additional Information:
- The team is preparing for an ISO Audit in October and requires expertise in ISO 13485 compliance.
- The Hiring Manager prefers candidates with realistic experience claims, avoiding exaggerated achievements (e.g., overstating QMS development).
- Candidates from CSUN's master's program in manufacturing (with a Green Belt certificate) have previously excelled in this role.
- The position is on-site atChatsworth, CA, transitioning to Los Angeles, CAby September/October.
- Candidates must be willing to work on-site, five days per week at both locations.
Interview Process:
- First Round: Virtual interview (Microsoft Teams) with the Hiring Manager.
- Second Round: On-site interview with the Hiring Manager, including a facility tour.
Manufacturing Quality Engineer Β· Macpower Digital Assets Edge Private Limited