Deputy Quality Manager
Quality 
Quality Manager
Purpose of the Job:
The Deputy Quality Manager is responsible for overseeing Quality Control (QC) in the Incoming Quality Control (IQC) process, Microbiological Testing, and Document Control and Standardization. The Deputy Quality Manager ensures compliance with established quality procedures and contributes to the implementation and maintenance of the company’s quality standards.
Key Responsibilities:

1.    Quality Control Management: Oversee IQC (Incoming Quality Control), ensuring the quality of raw materials and supplies. Manage the QC team in performing inspections and assessments at various stages of the production process.
2.    Incoming Quality Control (IQC): Supervise and manage the QC team responsible for incoming materials, ensuring that raw materials and components meet quality specifications. Establish and enforce IQC inspection standards, procedures, and acceptance criteria.
3.    Physical and Microbiology Laboratory Management: Oversee the operations of the  physical and microbiology laboratory activity entire, including Incoming material Quality Control (IQC), In-Process  product inspection and also final product inspection and laboratory activities, ensuring smooth and effective functioning of each unit.
4.    Document Control and Standardization: Develop and maintain quality-related documentation, including procedure manuals, standard operating procedures, work instructions, and other quality control documents to ensure compliance with internal and external standards. 
5.    Quality System Implementation: Assist the Quality Manager in the development, implementation, and maintenance of QMS. Contribute to the formulation of quality policies and objectives.
6.    Supplier Quality Management: Participate in supplier evaluations, establish supplier quality standards, and maintain control over the quality of raw materials and outsourced products. Address supplier-related quality issues and follow up on corrective actions to ensure supplier compliance.
7.    Measuring Equipment Calibration and Supervision: Establish and implement a system for the calibration and maintenance of measuring equipment, such as rulers, tape measures, and other tools. Supervise the testing and verification of measuring instruments to ensure accuracy and reliability.
8.    Quality Training and Development: Develop annual training plans for quality department personnel in collaboration with Quality Manager, focusing on enhancing technical skills, quality awareness, and compliance with quality standards. Implement training programs and evaluate their effectiveness.
9.    Departmental Goal Achievement: Coordinate and oversee the activities of the Quality Department in collaboration with the Quality Manager to ensure alignment with the company’s annual objectives. Drive departmental efforts to achieve quality-related goals and support the overall success of the organization in meeting its strategic targets.
10.    Interdepartmental Coordination and Communication: Facilitate communication and collaboration between the laboratory and other departments within the company to address quality-related issues and ensure cross-functional alignment.
11.    Compliance and Continuous Improvement: Ensure that the company’s quality management system complies with industry standards and customer requirements. Drive continuous improvement initiatives, identify opportunities for process enhancements, and implement best practices.
12.    Reporting and Documentation: Prepare and present quality performance reports, providing insights and recommendations for improvement. Maintain thorough documentation of quality activities, processes, and results.
13.    Other tasks: Complete additional tasks and projects as assigned by senior management to support the overall quality assurance objectives of the company.

Job Requirements

Qualifications:

Education: Bachelor’s degree, in Quality Management, Textile Engineering, Garment Engineering, Bio medical engineering and related fields
Experience: 8 years and above proven experience in quality management and quality control processes in a manufacturing environment, with at least 3 years in a similar role.
Skills: Strong understanding of quality standards, regulatory requirements, and quality assurance methodologies. Understand the ISO 13485 quality management system requirement.
Knowledge of medical device industry laws and regulations.
Proven ability to manage quality control teams and implement quality management systems effectively.
Excellent problem-solving, analytical, and decision-making skills.
Strong communication and interpersonal skills for effective collaboration with internal and external stakeholders.

How To Apply

Please use the following email addresses for CV submissions.

Rahel.Likinaw@et.lrmed.com

Betelhem.Sileshi@et.LRMed.com 

Job Requirements Candidates must hold a bachelor’s degree in Quality Management, Textile Engineering, Garment Engineering, Biomedical Engineering or related fields. They should have at least eight years of experience in quality management within manufacturing, with a minimum of three years in a similar supervisory role. How to Apply Use the email addresses below to submit your CV: Rahel.Likinaw@et.lrmed.com or Betelhem.Sileshi@et.LRMed.com