Job Description

For our client, a leading multinational manufacturer of aesthetics and physiotherapy devices, we are seeking an experienced Quality Control Officer to oversee all quality-related activities at their manufacturing facility in the Jebel Ali Free Zone. This role plays a key part in ensuring compliance with international quality standards, leading process improvements, and supporting regulatory requirements within the medical device manufacturing environment. At DNA Recruitment, we carefully review all applications and aim to contact every suitable candidate within max. 5 working days. If you don't hear from us, please consider your application unsuccessful on this occasion. Quality Control Officer - Job Responsibilities:

• Managing quality control functions in the medical equipment industry at a manufacturing site, handling complex projects, or implementing innovative quality initiatives.
• Preparing routine and special reports to staff, district management, and regulatory agencies as required.
• Coordinating or developing standard operating procedures for operations and field staff; preparing and/or maintaining computer programs for the compilation and statistical analysis of quality control data.
• Developing and presenting document training programs for laboratory, operations, and field staff on quality assurance, analyses, and safety; developing training protocols, competency standards, and documentation requirements.

Quality Control Officer - Job Requirements:

• Proficiency in quality control methodologies, statistical analysis tools, and quality management systems.
• Minimum 5-7 years of experience in quality control roles within the Manufacturing industry of Medical Equipment, including exposure to quality audits, process improvement projects, and regulatory compliance
• Possession of advanced quality certifications, leadership training programs, or specialized education in quality management disciplines.
• Strong communication skills, attention to detail, analytical thinking, problem-solving abilities, leadership qualities, and the ability to work effectively in a team environment.
• In-depth understanding of quality standards, regulatory requirements, GMP principles, and quality assurance best practices relevant to the Manufacturing sector.

If you have a strong background in quality control within medical device manufacturing and are ready to take on a leadership role, we encourage you to apply and join a team dedicated to excellence and innovation. DNA consultant in charge of this requisition: Agnieszka Bednarz CEEMEA Senior Research Consultant Apply for this position First Name * Last Name * Email * Phone (including country code) * Sex * Nationality * Country of Residence * Your Current Role * Your Current Monthly Salary * Your Desired Monthly Salary * Upload CV/Resume * Drop files here or click to uploadMaximum allowed file size is 5 MB. Allowed Type(s): .pdf, .docx Cover Letter By using this form you agree with the storage and handling of your data by DNA FZ LLC, as well as to receive an information about our Career Advancement Program by email. *