Compliance Supervisor

وصف الوظيفة


2024-11-24

Shift Work type

Compliance supervisor

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Job Description:

  • Ensure line clearance & cleaning checks of the batch manufacturing process.
  • Reviews documentation associated manufacture of products on the manufacturing area 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.
  • Performs in process control sampling, testing and inspection (as AQL) for all SEDICO and Toll Products.
  • Coordinates activities associated with deviation report 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 his unit or section are done according to the relevant cGMP and ISO standards (ISO 9001, ISO 14001, OHSAS 45001).

Job Requirement

  • Bachelor's degree in science or Pharmacy.
  • 5:7 years of relevant experience in sterile manufacturing in the pharmaceutical industry.
  • No less than 1 years in a similar position.
  • Up to date knowledge of current GMP, EDA Regulatory requirements, WHO & ICH guidelines
  • Excellent investigation and report writing skills.
  • Excellent problem-solving and analytical abilities.
  • Strong communication and interpersonal skills.

Working Conditions

  • Job Location: 6th of October City.
  • Shift work is required.

Benefits

  • Social Insurance.
  • Medical Insurance
  • Profit Share
  • Transportation is provided.

If you meet these qualifications and are interested in joining our team, please submit your resume and cover letter for consideration. to: [email protected] and mention in the subject " Fc- Compliance supervisor."

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