Private Label Quality Assurance Senior Specialist (2023130)
Nahdi Medical Co.
Date: 3 weeks ago
City: Jeddah
Contract type: Full time
Job Description
The QA Senior Specialist is responsible for detailed quality planning, both short term and long range, diagnosis of chronic quality problems (both internal and external), development of corrective action programs including but not limited to support on Quality Notifications, Change Controls, and validation activities. The position also is responsible for identifying and supporting Quality Assurance and Regulatory Compliance issues related to assigned product lines to assure compliance with FDA regulations, ISO standards, corporate directives and Company strategies.
Accountabilities
The QA Senior Specialist is responsible for detailed quality planning, both short term and long range, diagnosis of chronic quality problems (both internal and external), development of corrective action programs including but not limited to support on Quality Notifications, Change Controls, and validation activities. The position also is responsible for identifying and supporting Quality Assurance and Regulatory Compliance issues related to assigned product lines to assure compliance with FDA regulations, ISO standards, corporate directives and Company strategies.
Accountabilities
- Determines overall products quality by conducting and evaluating various product sampling tests and tests related.
- Examine and analyze team findings against measured service operational goals.
- Develop Product’s Inspection Plan.
- Performs audits to monitor compliance with all GMP standards, Food Safety Standards, Food Safety issues, Case and Label procedures and Safety programs and prepare suppliers evaluations Reports
- Lead the communications with Suppliers/ Laboratories and maintain all necessary documentations.
- Supervise Internal/ External Complaints related to PL products and coordinate with all stakeholders on resolutions actions
- Manage non-conformities (NCRs) and conducts initial investigations and assure timely executions for corrective actions.
- Assists in the development of special department projects in conjunction with DCs Quality Manage
- Consults with PL Commercial & DCs management on operational procedures to improve overall production efficiency related to PL and Import items
- Investigates reasons for complaints and if needed works closely with suppliers to identify the cause and define areas for improvement
- Ensure that all the process related to PL and Importation Department are updated and in line with company`s policies &, procedures
- Prepare and develop regular statistical reports to management to ensure business alignment.
- Indoors : 80%
- Outdoors : 20%
- Working Days : 5 Working Days
- Days off : 2 Days Off
- Working Hours : 8:00 AM – 5:00 PM (1 hour break)
- Education: BSc in chemistry, pharmacy.
- Experience: Min 3 years of experience in QA related to manufacturing or product development. Proffered to have cosmetics or pharmaceutical industry experience
- Computer Skills: MS Office Suite
- Languages: English - Arabic
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