Production Section Head

Hi Pharm - Obour City, Cairo

Applicants for
1 open position
Experience Needed:
3 to 5 years
Career Level:
Job Type:
Full Time
1 open position
About the Job
  • 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.
  • Ensure efficient collaboration and co-ordination between relevant departments according to the work needs

Job Requirements
  • BSc. degree in Pharmaceutical is a must.
  • Experience Required 3 to 5 Years.

About this Company

Hi Pharm is a customer centric company with a commitment to satisfying the patient’s unmet needs in medicine.

Through a leading portfolio & far reaching projects & programs to increase accessibility to our products & insure they reach the patients who need... (More)

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