إنتهت صلاحية هذا الإعلان الوظيفي لقد إنتهت صلاحية هذا الإعلان الوظيفي و هو غير مفتوح حاليا لأي طلبات عمل.
إرفاق
تصنيف الوظيفة
الأدوية
وصف الوظيفة
- Quality review of QC lab generated data and documentation for accuracy, completeness, and compliance in timely manner to meet the manufacturing schedules/ supply chain requirements.
- Audit trails review of analytical instrumentation to ensure data integrity.
- Raw data review for documented information such as calculation verification, standard/sample preparation, reagent preparation, instrument calibration, reagent expires, logbook entries, control charts, etc.
- Facilitates laboratory data or documentation corrections with analysts to ensure accuracy.
- Must have a working knowledge of the analytical instrumentations (HPLC, GC, UV-Vis, FTIR, KF, etc.) and able to understand and interpret chromatographic and other analytical data.
- Should have good command on Chromatographic Data Systems (Chromeleone/ Empower/ Labsolutions) software
- Assist laboratory to investigate any Out of Specification (OOS) and Out of Trend (OOT) results and deviations.
- Must be able to perform the trend analysis for the laboratory test results and suggest and implement CAPA’s.
- Create/ update Standard Operating Procedures (SOPs) as required.
- Provide support to Quality Assurance to perform Internal cGMP Audits.
- Completes other duties as assigned by Quality (QA/QC) management.
- To prepare and check Certificates of Analysis for all lots of finished product, raw materials and packaging materials tested in the QC Department.
- To provide training and retraining to new or existing laboratory staff on proper laboratory documentation procedures as required and ensure that this is documented according to procedures.
- To ensure GMP compliance as per local procedures, EU and USFDA guidelines.
- Assist with overall completion of QC Deviations, Errors, CAPA plans, Change controls and Risk Assessment.
- To review Calibration and qualification data for QC Laboratory Equipment/ Instruments.
- Responsible for continuous improvement in the warehouse department compliance.
- To ensure Safety norms as per EHS policy of the site, meet 100% guidelines.
- Shall be responsible for quality control operational excellence.
- Shall be accountable for timely completion of SOP and CGMP training.
المهارات
5 - 10 years of QC experience
Chemistry university degree
عن الشركة
Mezzan Holding Co.is one of the leading food, healthcare, and consumer conglomerates in the Middle East with a celebrated heritage of over 75 years.
Headquartered in Kuwait with direct operational activities in Kuwait, UAE, Qatar, Saudi Arabia, Iraq and Jordan
Mezzan Holding Co:
- Employs 8,500 people (50+ nationalities)
- Distributes over 34,000 Stock Keeping Units (SKU)
- Serves over 100,000 meals a day in Kuwait, Qatar and the UAE through its catering business.
- Has a total of 130,000 square meters in food, beverage and FMCG manufacturing facilities in Kuwait, Qatar, UAE.
- Represents some of the biggest names in the FMCG and healthcare industries.