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
- Strong understanding of USFDA/ MHRA/ EU or local guidelines
- Responsible for setting strategy direction for the entire Production Department and team.
- To enforce the batch manufacturing as per cGMP requirements in order to obtain high quality products.
- To achieve targeted production with span of control.
- To ensure the manufacturing equipment remains in validated stage
- To co-ordinate with interdepartmental functional to carry out day to day activities in a smooth manner minimizing loss of the manhours.
- To ensure maintenance plan of machines so as to reduce down time of machines which result in increase of product yield, productivity.
- Management and valuation of the work performed by the subordinate staff to ensure implementation of GMP standards and SOP
- To assure the in-house specification, SOPs and Master formulae and approvals.
- To ensure the Quality policies of the company and compliance.
- Readiness of production area for the Regulated Markets and lead the Regulatory audit team.
- Compilation of daily, weekly and monthly reports and their submission to the leadership team.
- To lead the plant’s Production plan & team towards the goal of the organization
- To ensure Safety norms as per EHS policy of the site, meet 100% guidelines.
- Preparation of department’s budget & its executions.
Communicating regularly with site leadership regarding problems or issues impacting production - Evaluating machine resources to ensure continued production and minimal downtime
- Establishing a balance between increased productivity and reduced costs of manufacturing operations by setting productivity goals for each manufacturing team
- Assess production standards in relation to plant capacity, materials supply, manpower availability and financial limitations.
- Ensures that proper manufacturing validation is being done at appropriate intervals.
- Ensures that all production equipment is maintained in good working order along with engineering department.
المهارات
- Prevous experience in the production of Sterile Injectables (Solution & Immersion Products)
- Understanding of Microbiology aspects of sterile manufacturing
- Skillful in managing a large team (50-80)
- Familiar with all Regulatory Audits (EMEA, MHRA & SFDA)
- SAP RM/PM Modules
عن الشركة
KSPICO we are Kuwait’s only pharmaceutical manufacturing company.
The products we manufacture are sold in Kuwait, distributed to most of the Middle East, and reach customers world-wide.
KSPICO is part of Mezzan Holding Co. 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
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- 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.