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Quality Control Manager

Pharco Corporation
Bourj Alarab, Alexandria
Pharco Corporation logo

Quality Control Manager

Bourj Alarab, AlexandriaPosted 2 days ago
13Applicants for1 open position
  • 0Viewed
  • 0In Consideration
  • 0Not Selected

Job Details

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Job Description

  • Laboratory Oversight
  • Manage daily operations of the QC laboratory (chemical, physical, and microbiological testing).
  • Ensure timely and accurate analysis of raw materials, intermediates, finished products, and stability samples.
     
  • Compliance and Documentation
  • Ensure full compliance with cGMP, GLP, and relevant regulatory guidelines.
  • Review and approve laboratory data, test results, CoAs, and protocols.
  • Maintain and audit QC documentation, ensuring data integrity and traceability.
     
  • Team Leadership and Development
  • Lead, train, and mentor QC analysts and technicians.
  • Evaluate staff performance and ensure continuous development and cross-training.

 

  • Method Validation & Transfer
  • Coordinate method validation, verification, and transfers in collaboration with R&D and QA.
  • Support new product introductions and scale-ups from a QC perspective.
     
  • Laboratory Equipment Management
  • Oversee calibration, maintenance, qualification, and lifecycle management of lab instruments.
  • Approve equipment qualification protocols and reports.

 

  • Investigation & Change Control
  • Lead OOS, OOT, deviations, CAPA, and laboratory investigations.
  • Support change control related to testing methods, materials, and specifications.
     
  • Audit Readiness and Support
  • Ensure QC area is inspection-ready at all times.
  • Act as SME during internal, customer, and regulatory audits.
     
  • Continuous Improvement
  • Identify and implement process improvements to enhance efficiency, accuracy, and compliance.

Job Requirements

  • Bachelor’s or Master’s degree in Pharmacy.
  • Minimum of 7–10 years of experience in a pharmaceutical QC environment, including at least 3 years in a leadership role.
  • Deep understanding of cGMP, and regulatory expectations.
  • Strong leadership, problem-solving, and communication skills.

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