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A global healthcare leader in Dubai is seeking a Quality Manager to ensure compliance with quality systems in the Middle East. Responsibilities include conducting audits, training staff, and managing quality documentation. Applicants should have a scientific background and at least 3 years of experience in quality assurance within the healthcare sector.
Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.
At Abbott, You Can Do Work That Matters, Grow, And Learn, Care For Yourself And Family, Be Your True Self And Live a Full Life. You Will Have Access To
Our Diagnostics business is looking for an Quality Manager to support Middle East and will be based in UAE.
We’re empowering smarter medical and economic decision making to help transform the way people manage their health at all stages of life. Every day, more than 10 million tests are run on Abbott’s diagnostics instruments, providing lab results for millions of people.
Ensure Quality System awareness and compliance of new and revised quality documents and regulations that affect the assigned area of responsibility.
Supports the business in the affiliate / region according to the position expertise and functions.
Plan and conduct internal audits to verify the effectiveness of the management system
Prepare / coordinate external audits.
Perform supplier audits as required.
Support / provide training to the organization about the CRDx Quality System.
Ensure QS record keeping, document control, Warehousing, QH, Supplier / Distributor evaluation / monitoring, CAPA management follow up and ensure timely closure.
Ensure availability of org charts (including LSME if required) and job descriptions.
Assess risk related to processes
Timely elevate regional concerns to Area Management Review and MIMS MR
Supports Global Commercial Affiliates QA improvement projects
Maintain / challenge current certifications. Propose new certificates if required.
Coordinates communication between commercial organization and Regulatory to support responses in contracts and public tenders (e.g. QARA, EHS, Data Privacy requirements).
Team / MIMS Subject Matter Expert & Procedure Owner : Be the expert on a QS process and support the rest of team as process SME : either as lead, backup or team member.
Review Abbott policies & procedures, and update Quality documentation accordingly.
Manage any audit input by initiating changes to affected processes following MIMS change control procedures.
Identify and coordinate improvement initiatives within the entire QS.
Participates in Quality System improvements and implementation projects
Actively seek internal / external customer feedback and respond to issues
If there is no regulatory function in the affiliate, perform / ensure revision and approval of locally / translated AdPromo material on behalf of Regulatory Affairs. If needed, support RA appointing language approvers and ensure trainings are done accordingly.
Manage the QA budget, always considering cost improvement opportunities.
Act as an expert for sales and customer support for accreditation topics, presentations, and process implementation in sites where customer certification / accreditation is requested.
Scientific background (i.e. Lab Technician, Biology, Chemistry, Pharmacy, M.D.) is preferred. Other education (i.e. business, engineer) is acceptable if experience of 3 or more years in similar manager position.
Background
Managers can have experience in one or several of the following :
Quality Assurance in a commercial affiliate at the IVD / MD / pharmaceutical industry is preferred, either as manager or as specialist, for at least 3 years.
Regulatory Affairs, Customer Service or any other commercial affiliate function at the diagnostic / medical device / pharmaceutical industry,
Manufacturing / Distribution / Clinical laboratory / Competent Authority / IVD / MD / Pharma industry association
This is the experience expected for each category,
Product and market environment knowledge preferred.
Management skills and leadership competencies
Experience to work in international environment, project management and negotiation skills desirable.
Operates under Quality and Regulatory directives and Abbott policies and procedures.
Follows local regulations, European guidelines, and International Industry / Quality System standards.