Deputy Production Manager at Macro Group
Maintain work flow by monitoring steps of the process; setting processing variables; observing control points and equipment; monitoring personnel and resources; studying methods; implementing cost reductions; developing reporting procedures and systems; facilitating corrections to malfunctions within process control points; initiating and fostering a spirit of cooperation within and between departments.
Complete production plan by scheduling and assigning personnel; accomplishing work results; establishing priorities; monitoring progress; revising schedules; resolving problems; reporting results of the processing flow on shift production summaries.
Maintain quality service by establishing and enforcing organization standards.
Ensure operation of equipment by calling for repairs; evaluating new equipment and techniques.
Maintain professional and technical knowledge by attending educational workshops; reviewing professional publications; establishing personal networks; bench marking state-of-the-art practices; participating in professional societies.
Maintain safe and clean work environment by educating and directing personnel on the use of all control points, equipment, and resources; maintaining compliance with established policies and procedures.
Resolve personnel problems by analyzing data; investigating issues; identifying solutions; recommending action.
Ensure line clearance & cleaning checks of the batch manufacturing process
Reviews documentation associated manufacture of products on the manufacturing floor during production.
Work closely with manufacturing to address any production issues on shift and ensure appropriate documentation.
Coordinates and assembly of batch record documentation to assist with disposition.
Reviews and approves completed manufacturing related documents for batch record disposition.
Coordinates activities associated with deviation resolution and CAPAs to facilitate investigations and assure timely closure.
Ensures adherence of appropriate cGMP regulations and quality standards.
Perform or support any other tasks necessary to maintain the product quality and site cGMP compliance, as needed.
Ensures that all activities in the unit or section are done according the relevant cGMP and ISO standards (ISO 9001/2015, ISO 14001/2015, and OHSAS 18001/2007).
Organize and implement the handling of production wastes.
BSc. degree in Pharmacy , Science is a must.
Experience Required 5 to 8 Years.
Can Work Under Stress
Fluent in English
Very good Computer Skills